Publications and Presentations



[ From IIT Bombay ]




2016


    66. "Recent Trends in Copper-Catalyzed C-H Amination Routes to Biologically Important Nitrogen Scaffolds". Parthasarathi Subramanian, Georg C. Rudolf, and Krishna P. Kaliappan, Chem.Asian.J., 2016, 11, 168-192.  DOI :



    65. "A Copper Catalyzed Cascade Amination Route to N-Aryl Benzimidazoquinazolinones". Arpan Banerjee, Parthasarathi Subramanian and Krishna P. Kaliappan. J.Org.Chem., J. Org. Chem. 2016, 81, 10424-10432.  DOI :

    An efficient one-pot Cu-catalyzed C-H functionalization/two-fold C-N bond formation protocol for the syntheses of N-aryl benzimidazoquinazolinones is being reported. This strategy involves a Cu-catalyzed C-N bond coupling reaction between N-anilinoquinazolinones and aryl/heteroaryl halides followed by acetate ligand assisted intramolecular C-H amination. This reaction is general and straightforward for the synthesis of anti-cancer drug analogs of benzimidazoquinazolinones.




2015


    64. "An enantioselective total synthesis of Sch-725674". Kota Ramakrishna and Krishna P. Kaliappan, Org. Biomol. Chem., 2015, 13, 234-240.  DOI

    An enantioselective total synthesis of Sch-725674, a unique 14-membered macrolactone, has been accomplished in 13 steps. The step-wise dithiane alkylation served as a strategic step to assemble the upper and lower fragments of the molecule, whereas cross metathesis reaction, Yamaguchi macro-lactonization and a substrate controlled stereoselective reduction are used as key steps to complete the total synthesis.





2014


    63. "A One-Pot Copper Catalyzed Biomimetic Route to N-Heterocyclic Amides from Methyl Ketones via Oxidative C-C Bond Cleavage". Parthasarathi Subramanian, Satrajit Indu and Krishna P. Kaliappan, Org. Lett., 2014, 16 (23), 6212-6215.   DOI

    A direct one-pot Cu-catalyzed biomimetic oxidation of methyl ketones to pharmaceutically important N-heterocyclic amides is reported. The scope of the method is broad, scalable, and mild, and the reaction is tolerant with various acid, base sensitive functionalities with multiple heteroatoms and aryl halides. The extensive mechanistic studies suggest that this reaction follows the Luciferin-Luciferase-like pathway.




    62. "A Domino Enyne/IMDA Approach to the Core Structure of (-) Vinigrol". Vipul V. Betkekar, Ashik A. Sayyad and Krishna P. Kaliappan, Org. Lett., 2014, 16(21), 5540-5543 DOI :

    We report here an enantioselective formal synthesis of vinigrol involving a 1?2?3 strategy: one pot and tworeactions with the formation of three rings leading to the core structure of vinigrol from its stereochemically well-defined acyclicprecursor.




    61. "Transition Metal Catalyzed Selective Cyclization Strategy to 2-Substituted Benzofurans and Indoles En-Route to the Oxa-Analogs of Isocrytolepine". Satrajit Indu, Parthasrathi Subramanian and Krishna P. Kaliappan, Eur. J. Org. Chem., 2014,7193-7202. DOI :

    We have described a selective cyclization strategy towards 2-substituted benzofurans and indoles starting from similar starting materials. Substrates having free -NH2 groups, which are traditionally reluctant to undergo Sonogashira coupling reactions have been shown to give good yields. The benzofurans have been further improvised to prepare the oxa-analogs of the natural product isocryptolepine.




    60. "A Unified Strategy Towards N-Aryl Heterocycles by a One-Pot Copper-Catalyzed Oxidative C-H Amination of Azoles". Parthasarathi Subramanian and Krishna P. Kaliappan, Eur. J. Org. Chem., 2014, 5986-5997. DOI:

    An efficient one-pot synthesis of N-aryl-substituted heterocycles by a Cu-catalyzed two-fold C-N bond formation is reported. This strategy involves a CuI-catalyzed C-N bond-forming reaction between azoles and electron-deficient bromopyridines followed by an intramolecular sp2 C-H amination. One of the products thus formed has been successfully used as a ligand for the synthesis of a Pd complex.



    59. "Total syntheses of rubiginone A2, C2, andfujianmycin A". Devendar G. Vanga and Krishna P. Kaliappan, RSC Adv., 2014, 4, 12716-12722. DOI :

    The total syntheses of rubiginone A2, C2 and fujianmycinA are described. The synthesis involves Diels-Alder/aromatization and photo chemical reactions as key steps to construct the tetracyclic frame ofbenz[a]anthraquinone skeleton. Sharplessepoxidation, a copper-catalyzed regioselective epoxideopening, and enyne metathesis reactions are utilized as the key steps for the synthesis of chiralvinylcyclohexene.




    2013


    58. "Kinugasa Reaction: A Direct One Pot Route to Highly Functionalized β-Lactams." Rama K. Khangarot and Krishna P. Kaliappan, Eur. J. Org. Chem., 2013, 7664-7677. DOI.

    The β-lactam antibiotics are among the most commonly prescribed drugs in the world and their importance has been demonstrated by the isolation and syntheses of several classes of these agents. Of the synthetic routes used to access this interesting scaffold, the Kinugasa reaction utilizes a convergent strategy based on cycloaddition between readily available terminal alkynes and nitrones. Asymmetric versions involving chiral catalysts, chiral auxiliaries or chiral substrates have also been reported. This article gives a brief overview of the Kinugasa reaction and of recent advances since its discovery.

    57. "A hybrid approach to new molecular scaffolds" Kalanidhi Palanichamy and Krishna P. Kaliappan, Pure Appl. Chem., 2013, 85, 1185-1202. DOI :

    Our various efforts toward the synthesis of a set of novel sugar hybrid scaffolds of several biologically active natural products such as taxol, steroids, ?-lactams, and otteliones are presented. We have shown the application of the hybrid approach to design and rapidly generate a library of novel natural product-like compounds, which may have interesting biological features, using metathesis and/or cycloaddition reactions as key steps.

    56. "A Stereoselective Synthesis of Trifluoromethyl-Analogues of Polyhydroxy Pyrrolidines" Rama K. Khangarot and Krishna P. Kaliappan, Eur. J. Org. Chem., 2013, 2692-2698. DOI :

    An efficient strategy for the synthesis of a variety of trifluoromethylated polyhydroxypyrrolidines is described. This strategy involves a diastereoselective nucleophilic addition reaction of trimethyl(trifluoromethyl)silane to sugar-derived cyclic nitrones followed by reductive N-O bond cleavage and removal of benzyl groups.



    55. "A One-Pot, Copper-Catalyzed Cascade Route to 2-Indolyl-C-glycosides" Parthasarathi Subramanian and Krishna P. Kaliappan, Eur.J. Org. Chem., 2013, 595-604. (Highlighted in CHEMISTRYVIEWS on 06 Dec 2012). DOI :

    An efficient and high-yielding, one-pot, Cu-catalyzed synthesis of 2-indolyl-C-glycosides is delineated. The sequence involves a cascade Sonogashira type coupling and a hydroamination reaction between sugar-derived alkynes and N-tosyl-o-iodoaniline followed by the removal of the N-tosyl group to provide a library of 2-indolyl-C-glycosides in moderate to excellent yields.




    2012


    54. "Recent Developments on Domino Metathesis Reactions in India" Rahul S. Nandurdikar and Krishna P. Kaliappan, CHIMIA 2012, 66,892-896

    53. "Total Synthesis and Stereochemical Assignment of (-)-Zenkequinone B" Vanga Devendar Goud and Krishna P. Kaliappan, Synlett 2012, 23, 2931-2934. DOI :

    The first enantioselective total synthesis and a concise racemic synthesis of zenkequinone B are reported here by utilizing a sequential enyne metathesis, Diels-Alder and aromatization reactions.



    52. "A Concise Total Synthesis of (+)-Cladospolide D" D. Si and Krishna P. Kaliappan Synlett 2012, 23, 2822-2826. DOI :

    A short and convergent total synthesis of (+)-cladospolide D is delineated, which involves olefin cross metathesis andfuran oxidation to access the ?-oxo-?,?-unsaturated acid and Yamaguchi lactonization to construct the 12-membered ring as key steps.



    51. "A Stereoselective Route to Aza-C-aryl Glycosides from Arynes and Chiral Nitrones" Rama K. Khangarot and Krishna P. Kaliappan, Eur. J. Org. Chem., 2012, 5844-5854. DOI :

    An efficient strategy for the synthesis of a variety of aza-C-aryl glycosides is described. This strategy involves a stereoselective 1,3-dipolar cycloaddition reaction between arynes and sugar-derived cyclic nitrones followed by reductive N-O bond cleavage and removal of benzyl groups.





    50. "Synthetic Utility of Sugar Derived Cyclic Nitrones: A Diastereoselective Synthesis of Linear 4-Azatriquinanes" Anandaraju Bandaru and Krishna P. Kaliappan, Synlett 2012, 1473-1476. DOI :

    A diastereoselective Pauson-Khand reaction has been utilized as the key step in the construction of azatriquinanes from sugar-derived nitrones.



    49. "An Efficient Copper Catalyzed 3-Component Synthesis of 3-C-Linked Glycosyl Iminocoumarins" Kalanidhi Palanichamy, Sankar R. Suravarupu, Krishna P. Kaliappan, Synthesis, 2012, 1841-1848. DOI :

    An efficient general strategy was developed for the synthesis of previously unknown 3-C-linked glycosyl iminocoumarins. The strategy involves a copper-catalyzed multicomponent reaction of sugar-derived alkynes with tosyl azide and salicylaldehyde to give a diverse array of glycosyl iminocoumarins in good yields. These compounds can serve as appropriate precursors for the synthesis of the corresponding coumarin 3-C-glycosides.



    48. "A Tandem Enyne/Ring Closing Metathesis Approach to 4-Methylene-2-cyclohexenols: An Efficient Entry to Otteliones and Loloanolides" Vipul V. Betkekar, Samaresh Panda and Krishna P. Kaliappan, Org. Lett., 2012, 14, 198-201. DOI :

    A short and efficient approach to a 4-methylene-2-cyclohexenone substructure present in otteliones and loloanolides is described. This strategy involves a tandem enyne/ring closing metathesis as the key reaction to construct this labile core unit.



    47. "An Iterative Shimizu Non-aldol Approach for the Stereoselective Synthesis of C13-C22 Fragment of Callystatin A" Sandip A. Pujari and Krishna P. Kaliappan, Org. Biomol. Chem., 2012, 1750-1753

    An efficient synthesis of the polypropionate framework of callystatin A has been achieved by utilizing the Shimizu reaction in an iterative fashion.



    Link :

    46. "A Unified Strategy for the Syntheses of Angucyclinone Antibiotics: Total Syntheses of Tetrangulol, Kanglemycin M, X-14881-E and Anhydrolandomycinone" Vanga Devendar Goud and Krishna P. Kaliappan, Eur.J. Org. Chem., 2012, 2250-2259 DOI :

    A unified strategy that involves sequential intramolecular enyne metathesis, Diels-Alder, photooxygenation, and aromatization reactions has been developed for the syntheses of angucyclinone antibiotics.




2011


    45. "A One Pot Deprotection and Intramolecular Oxa Michael Addition to Access Angular Trioxatriquinans". K. Ramakrishna and Krishna P. Kaliappan, Synlett 2011, 2580-2584

    An efficient one-pot deprotection-oxa-Michael addition strategy has been used to synthesize a few trioxatriquinanes starting from commercially available sugars.



    Link :

    44. "A Radical Approach to Formal Total Syntheses of Platencin". K. Palanichamy A. V. Subrahmanyam and Krishna P. Kaliappan, Org. Biomol. Chem. 2011, 9, 7877-7886.

    Two different strategies leading to formal total syntheses of platencin are described. The first strategy involving Claisen rearrangement and radical cyclization provides a rapid access to the core structure of platencin, and also use minimum protective-group operations. The second strategy, a protecting group-free route, utilizes a 6-exo-trig radical cyclization and aldol condensation as key steps leading to the formal synthesis of platencin.



    Link :

    43. "A Shimizu Aldol Approach to Formal Total Synthesis of Palmerolide A." S. A. Pujari, P. Gowrisankar and Krishna P. Kaliappan, Chem. Asian. J. 2011, 6, 3137-3151. DOI :

    A convergent and efficient formal total synthesis of palmerolide A has been achieved. This synthetic approach involves a coupling of three fragments involving Julia-Kocienski olefination, Yamaguchi esterification, and ring-closing metathesis (RCM) reactions as key steps.



    42. "A Flexible and Unified Strategy for Syntheses of Cladospolides A, B, C and iso-Cladospolide B." Debjani Si, Narayana M. Sekar and Krishna P. Kaliappan, Org. Biomol. Chem. 2011, 9, 6988-6997.

    A simple, efficient and flexible strategy for the syntheses of cladospolides A-C and iso-cladospolide B is reported here. This strategy involves Julia-Kocienski olefination and Yamaguchi macrolactonization as key steps, starting from either D-ribose or suitable tartaric acid esters. Although our initial efforts towards cladospolide A involving a ring closing metathetic approach were not successful, changing the mode of ring closure and the use of Julia-Kocienski olefination for the construction of the key intermediate solved this issue and paved the way for the completion of total syntheses of this class of natural products.



    Link :

    41. "A Stereoselective Synthesis of Sugar Derived Chiral β-Lactams ."Rama K. Khangarot and Krishna P. Kaliappan<, Eur. J. Org. Chem., 2011, 6117-6127. DOI :

    A variety of sugar-derived chiral ?-lactams have successfully been synthesized in moderate to good yields and with high diastereoselectivity by the Kinugasa reaction between sugar-derived cyclic nitrones and alkynes.






2010


    40. "Application of Enyne Metathesis/Diels-Alder Cycloaddition Sequence: A New Versatile Approach to Syntheses of C-Aryl Glycosides and Spiro C-Aryl Glycosides." A. V. Subrahmanyam, P. Kalanidhi, Krishna P. Kaliappan Chem. Eur. J. 2010, 16, 8545-8556. DOI :

    Simple sequence for a difficult task! A sequential enyne metathesis/Diels-Alder reaction/aromatization strategy has been developed to access the synthesis of a library of C-aryl and spiro-C-aryl glycosides (see scheme). This strategy has also been extended to the synthesis of a set of hybrids of C-aryl and spiro-C-aryl glycosides.



    39. "A Formal Total Synthesis of Palmerolide A." P. Gowrisankar, S. A. Pujari, Krishna P. Kaliappan Chem. Eur. J. 2010, 16, 5858-5862. DOI :

    An efficient formal total synthesis of the marine natural product palmerolide A is reported herein, involving 24 longest linear steps. The key features of our synthesis involve a combination of Sharpless epoxidation and Shimizu reaction to construct the syn aldol moiety, a Julia-Kocienski reaction to construct the diene, and ring-closing metathesis to form the macrocycle (see scheme; PG=protecting group).



    38. "Synthesis of a Novel Taxa-Oxa-Sugar Hybrid Core Structure by Tandem Cross Enyne Metathesis/IMDA." R. S. Nandurdikar, A. V. Subrhamanyam, Krishna P. Kaliappan Eur. J. Org. Chem., 2010, 2788-2799. DOI :

    This paper describes our design and efforts in synthesizing new scaffolds with taxol-eleutherobin hybrid core structures and a taxol-sugar hybrid. The synthesis of taxol-eleutherobin hybrids involved the synthesis of the A-ring fragment from carvone and the C-ring fragment from either D-mannose or D-glucose. The Shapiro reaction was used as the key reaction to couple the A- and C-ring fragments of these hybrid structures. Unfortunately, another key reaction (RCM) failed to form the B-ring and essentially the core unit. However, a tandem enyne cross-metathesis/intramolecular Diels-Alder strategy was utilized for the synthesis of a taxa-oxa-sugar hybrid.



    37. "Discovery and Syntheses of Superbug Challengers-Platensimycin and Platencin." K. Palanichamy, Krishna P. Kaliappan Chem. Asian J. 2010, 668-703. DOI :

    Bacteria have developed resistance to almost all existing antibiotics known today and this has been a major issue over the last few decades. The search for a new class of antibiotics with a new mode of action to fight these multiply-drug-resistant strains, or "superbugs", allowed a team of scientists at Merck to discover two novel antibiotics, platensimycin and platencin using advanced screening strategies, as inhibitors of bacterial fatty acid biosynthesis, which is essential for the survival of bacteria. Though both these antibiotics are structurally related, they work by slightly different mechanisms and target different enzymes conserved in the bacterial fatty acid biosynthesis. This Focus Review summarizes the synthetic and biological aspects of these natural products and their analogues and congeners.




    2009


    36. "A Versatile Access to Calystegine Analogues as Potential Glycosidases Inhibitors." Krishna P. Kaliappan, P. Das, S. T. Chavan, S. G. Sabharwal J. Org. Chem., 2009, 74, 6266-6274 DOI :

    An efficient metathetic strategy and nitrone chemistry have been suitably tethered to construct 8-azabicyclo[3.2.1]octanes as versatile precursors for the synthesis of several calystegine analogues. This synthetic strategy relies on the ability of mannose-derived nitrone to undergo a highly stereoselective nucleophilic addition of various Grignard reagents to access syn orientation of alkenes, which then smoothly undergo ring-closing metathesis (RCM) to provide this framework. These RCM products 18 and 20 have been successfully used as advance precursors to synthesize many calystegine analogues either by syn-dihydroxylation or by hydrogenation and followed by global deprotection. Interestingly, both compounds 36 and 40 exhibited significant noncompetitive inhibition against ?-mannosidase and N-acetyl-?-D-gluco-saminidase.



    35. "An Expedient Total Synthesis of (-)-Cladospolide A." Krishna P. Kaliappan and D. Si Synlett 2009, 2441-2444.

    A simple and efficient total synthesis of (-)-cladospolide A is described here, which involves either olefin cross metathesis or Julia-Kocienski olefination and Yamaguchi macrolactonization as key steps.



    Link :

    34. "Click Chemistry on Sugar Derived Alkynes: A Tandem Click-Click Approach to Bistriazoles." Krishna P. Kaliappan, P. Kalanidhi and S. Mahaptra Synlett 2009, 2162-2166

    Development of a tandem 'click-click' approach to the formation of successive 1,4-disubstituted 1,2,3-triazole linkages and 'click chemistry' on sugar-derived alkynes are described.



    Link :



    2008


    33. "A Rapid Access to New Fluorinated 1,3-Dienes and Benzylic Fluorides via Metathesis on Propargylic Fluorides." Sandip A. Pujari, Krishna P. Kaliappan, Allan Valleix, Danielle Gree and Rene Gree Synlett 2008, 2503-2507.

    The cross enyne metathesis reaction of propargylic fluoride (+)-12 with ethylene affords the enantioenriched 1,3-diene (+)-14 having fluorine-containing side chain at 2-position in good yield. Upon Diels-Alder reaction, followed by aromatization, this diene affords the new benzylic fluorides (+)-16 and (+)-17 in high ee values. This new strategy has been successfully extended to the corresponding gem-difluoro diene 21 and benzylic fluorides 23 and 24.



    Link :

    32. "Cope-House Cyclization Strategy for the Synthesis of Pyrrolizidines: An Expedient Route to 5-epi-Hyacynthacine A3 and A5." Krishna P. Kaliappan and P. Das Synlett 2008, 841-844.

    An expedient Cope-House cyclization strategy is reported here for the synthesis of several polyhydroxy pyrrolizidine alkaloids starting from sugar-derived nitrones.



    Link :

    31. "Synthetic Studies on Taxanes: A Domino Enyne Metathesis/Diels-Alder Approach to the AB ring." Krishna P. Kaliappan Velayutham Ravikumar and Sandip A. Pujari J. Chem. Sci. 2008, 120, 205-216.

    A domino enyne cross-metathesis/intramolecular Diels-Alder reaction has been successfully used to synthesize a bicyclo[5.3.1]undecene, corresponding to AB-ring of taxol without the gem di-methyl group.

    Link :


    2007


    30. "Angucylinone Antibiotics: Total Syntheses of YM -181741, (+)-Ochromycinone, (+)-Rubiginone B2, (-)-Tetrangomycin and MM-47755." Krishna P. Kaliappan and V. Ravikumar J. Org. Chem., 2007, 6116-6126. DOI :

    A concise and highly enantioselective route has been developed for the synthesis of angucyclinone-typenatural products. Utilizing this strategy, total syntheses of five natural products YM-181741, (+)-ochromycinone, (+)-rubiginone B2,(-)-tetrangomycin, and MM-47755 have been accomplished in 22%,23%, 19%, 18%, and 12% overall yields, respectively. Our approach for the synthesis of these naturalproducts having the benz[a]anthraquinone skeleton is based on a sequential intramolecular enynemetathesis, intermolecular Diels-Alder reaction (DAR), and aromatization. The intramolecular enynemetathesis reaction was employed for the synthesis of enantiopure 1,3-dienes in excellent yields.Furthermore, the synthesis of YM-181741 as well as structurally similar angucyclinones such as (+)-ochromycinone and (+)-rubiginone B2was achieved via asymmetric enolate alkylation of an oxazolidinonein excellentde. The related angucyclinones (-)-tetrangomycin and MM-47755, bearing a labile tertiaryalcohol, were synthesized via Sharpless asymmetric epoxidation of a known allylic alcohol followed byopening the epoxide with Red-Al. The introduction of oxygen functionality at C-1 in all these naturalproducts was accomplished by photooxygenation under a positive pressure of oxygen.





    29. "An Expedient Enantioselective Strategy for the Oxatetracyclic Core of Platensimycin." Krishna P. Kaliappan and V. Ravikumar Org. Lett., 2007, 9, 2417-2430. DOI :

    An enantioselective route for the synthesis of oxatetracyclic core of platensimycin is reported for the first time using a 5-exo-trig cyclizationfollowed by intramolecular etherification as key reactions. The requisite dienynone for the radical cyclization is synthesized in eight stepsfrom the Wieland?Miescher ketone employing a Claisen rearrangement.





    28. "Synthetic Studies on a Marine Natural Product Palmerolide A: Synthesis of C1-9 and C15-21 fragments." Krishna P Kaliappan and P. Gowrisankar, Synlett 2007, 1537-1540.

    An efficient cross metathesis and Pd-catalyzed allylic re-arrangement have been successfully used to construct the northern hemisphere of a cytotoxic marine natural product, palmerolide A.



    Link :

    27. "First Enantioselective Total Synthesis of the Angucyclinone-Type Anitbiotic YM-181741." Krishna P. Kaliappan and V. Ravikumar Synlett 2007, 977-980.

    A simple and efficient strategy for angucyclinone anti-biotics is described with the disclosure of first total synthesis of YM-181741.



    Link :

    26. "A New Versatile Strategy for C-Aryl Glycosides." Krishna P. Kaliappan and A. V. Subrahmanyam Org. Lett., 2007, 9, 1121-1124. DOI :

    A versatile strategy involving a sequential intermolecular enyne metathesis of C-alkynyl glycosides with ethylene, Diels?Alder, and aromatization reactions is successfully developed to provide a range of C-aryl glycosides.






    2006


    25. "A Tandem Enyne-Ring Closing Metathesis Approach to the Synthesis of Novel Angularly Fused Dioxatriquinanes." Krishna P. Kaliappan R. S. Nandurdikar and M. M. Shaikh Tetrahedron 2006, 62, 5064-5073.

    Triquinanes and their oxygenated congeners, oxa- and dioxa-triquinanes, exhibit versatile biological activities in conjunction with synthetically challenging molecular architecture. Owing to these properties, several new strategies have been developed to accomplish the synthesis of these sesquiterpenes. Among the new strategies, cascade radical cyclization strategy has been broadly explored and well studied. Herein, we report our efforts in detail for the synthesis of dioxa-triquinanes using a domino enyne/RCM strategy as the key step. Carbohydrate based synthesis not only allows the use of inexpensive and optically pure starting materials, but also the furanose derivatives, which already possess one of the requisite dihydro-furan moieties in the desired dioxa-triquinane. The other two five-membered rings were constructed simultaneously by the cascade enyne/RCM reaction using the Grubbs' second-generation catalyst. During the course of our synthesis it was observed that the acetonide protection hinders the RCM reaction, after the initial enyne metathesis reaction. The reaction underwent smoothly under argon atmosphere, whilst use of ethylene atmosphere was found to hinder the formation of the tandem enyne/RCM product. The effect of substitution on the key reaction is described here.



    Link :

    24. "Synthesis of a Bicyclo[5.3.1]undecene by a Facile Domino Enyne Cross Metathesis/IMDA." Krishna P. Kaliappan, V. Ravikumar and S. A. Pujari Tetrahedron Lett., 2006, 47, 981-984.

    An efficient domino cross-enyne metathesis/intramolecular Diels-Alder reaction is demonstrated for the construction of a bicyclo[5.3.1]undecene.



    Link :




    2005


    23. "A Facile Domino Metathetic Route to Thapsigargin Skeleton." Krishna P. Kaliappan and R. S. Nandurdikar, Org. Biomol. Chem. 2005, 3, 3613-3614.

    A facile synthesis of a 5,7,5-fused ring system that is presentin thapsigargins belonging to a novel family of sesquiterpene lactones, guainanolides, using domino enyne-RCM isreported here.



    Link :

    22. "Recent Advances in Cascade Enyne/RCM in Organic Synthesis." Krishna P. Kaliappan, Letters in Organic Chemistry, 2005, 2, 678-686. DOI :

    A concise highlight on recent advances in cascade/enyne RCM reactions of a range of substrates is discussed. Some of the reported strategies led to total synthesis of biologically active natural products.

    21. "Efficient Metathesis Route to the B-ring of Eleutherobin and Other Medium-Sized Cyclic Ethers." Krishna P. Kaliappan and N. Kumar, Tetrahedron 2005, 61, 7461-7469.

    A short and efficient RCM route is reported for the synthesis of the B-ring of eleutherobin and other medium-sized cyclic ethers from readily available 1,2,5,6-diisopropylidene-D-glucose. This strategy is successfully extended to the synthesis of a few bicyclic ethers, which may find applications in the synthesis of novel bicyclic nucleosides.



    Link :

    20. "Design and Synthesis of Novel Oxa-bridged Isoxazolidines and 1,3-Aminoalcohols." Krishna P. Kaliappan, P. Das and N. Kumar, Tetrahedron Lett. 2005, 46, 3037-3040.

    An expedient intramolecular olefin-nitrone cycloaddition (INC) route is reported for the synthesis of a series of noveloxa-bridged isoxazolidines and 1,3-aminoalcohols starting fromD-(+)-mannose-derived nitrones.



    19. "Design and Synthesis of Novel Sugar-Oxasteroid-Quinone Hybrids." Krishna P. Kaliappan and V. Ravikumar, Org. Biomol. Chem. 2005, 3, 848-851.

    A new class of sugar-oxasteroid-quinone hybrid molecules has been designed and synthesized involving an efficient enyne metathesis/Diels-Alder reaction strategy.



    Link :


    2004


    18. "A Cascade Enyne/RCM Approach to Angularly Fused Dioxatriquinanes." Krishna P. Kaliappan and R. S. Nandurdikar, Chem. Commun. 2004, 2506-2507.

    An expedient and first tandem enyne/ring closing metathesis approach on a sugar furanose template leading to a novel angularly fused dioxa-triquinane is described here.



    Link :

    17. "An Expedient Enyne Metathesis Approach to Dysidiolide." Krishna P. Kaliappan and P. Gowrisankar, Tetrahedron Lett. 2004, 45, 8207-8209.

    A short and efficient enyne metathesis route is reported for the construction of a key intermediate required in thesynthesis of dysidiolide thus completing its formal synthesis.



    Link :




    2003


    16. "A Ring Closing Metathesis Approach to a Synthesis of the B-ring of Eleutherobin." Krishna P. Kaliappan and N. Kumar, Tetrahedron Lett. 2003, 44, 379-381.

    A short and efficient RCM route is reported for the construction of the key nine-membered B ring of eleutherobinstarting from the readily available 1,2,5,6-diisopropylidene-D-glucose.



    Link :







[ From Duke University, USA ]



    15. "Combinatorial Discovery of Two-Photon Photoremovable Protecting Groups." Michael C. Pirrung, Wolfgang H. Pieper, Krishna P. Kaliappan and M. R. Dhananjeyan, Proc. Natl. Acad. Sci. USA , 2003, 12553-12558.

    A design principle for a two-photon photochemically removableprotecting group based on sequential one-photon processes hasbeen established. The expected performance of such groups inspatially directed photoactivationphotodeprotection has beenshown by a kinetic analysis. One particular molecular class fittinginto this design, the nitrobenzyl ethers ofo-hydroxycinnamates,has been presented. An initial demonstration of two-photondeprotection of one such group prompted further optimizationwith respect to photochemical deprotection rate. This was accomplished by the preparation and screening of a 135-member indexedcombinatorial library. Optimum performance for>350 nm deprotection in organic solvent was found with 4,5-dialkoxy and -cyanosubstitution in the nitrobenzyl group and 4-methoxy substitutionin the cinnamate.

    Link :

    14. "Dipolar Cycloaddition of Rhodium generated Carbonyl ylides with p-Quinones". M. C. Pirrung and Krishna P. Kaliappan, Org. Lett. 2000, 353-355. DOI :

    The dipolar cycloaddition of carbonyl ylides generated by the rhodium-catalyzed decomposition of ?- and ?-carbonyl-?-diazoketones with p-quinones leads to both C=O and C=C addition products. The product ratio is solvent- and catalyst-dependent and has been optimized to favor formation of either product. The C=C addition products of naphthoquinones are used in the assembly of structures hybridizing the illudin and anthraquinone anticancer agents.



    13. "Pirrung, M. C.; Krishna P Kaliappan. Dipolar cycloaddition of rhodium-generated carbonyl ylides with p-quinones." Book of Abstracts, 219th ACS National Meeting, San Francisco, CA, March 26-30, 2000 (2000), ORGN-835.





[ From University of Geneva, Switzerland ]



    12. "Synthesis of [6,n] cis-fused ring compounds via Cr-mediated dearomatization-ring-closing metathesis." E. P. Kundig, A. Bellido, Krishna P. Kaliappan, A. R. Pape and S Radix, Org. Biomol. Chem. 2006, 4, 342-351.

    Temporary complexation of an arene to the Cr(CO)3 fragment provides rapid access to the cis-fused [6,8], [6,7], [6,6] and [6,5] ring systems shown; starting from chiral complexes products are obtained with 88 to >98% de.



    Link :

    11. "Efficient Access to Fused Ring Compounds via Dearomatization/Ring-Closing Metathesis." E. P. Kundig, A. Bellido, Krishna P. Kaliappan, A. R. Pape and S Radix, Synlett, 2003, 2407-2409. DOI :

    The complex (p-methoxyphenyl oxazoline)Cr(CO)3 is converted in two steps into a cis-fused [6,8] ring system containing a cycohexadiene ring unit, a cyclooctenone ring and a quaternary carbon at the ring junction. The key steps involve a diastereoselective addition of three C-substituents across an arene double bond, followed by an allylation and ring closing metathesis step. cis-Fused [6,7], [6,6], and [6,5] ring systems are also accessible via this methodology.

    10. "Transition metal-mediated Dearomatization reactions." A. R. Pape, Krishna P. Kaliappan and E. P. Kundig, Chem. Rev. 2000, 2917-2940. DOI :

    9. "Planar Arene Cr(CO)3 in Organic Synthesis". Krishna P. Kaliappan, E. P . Kundig, H. Ratni and D. M. Sigano. Chimia, 1998, (52), 482.




[ From Indian Institute of Science, Bangalore ]



    8. "Synthetic Studies Towards the Nortriterpene Pfaffic Acid: Synthesis of DEF Fragment via Tandem Radical Cyclization Rearrangement Reactions." P. J. Biju, Krishna P. Kaliappan and G. S. R. Subba Rao, Arkivoc, 2004, viii, 37-45.

    A tandem 5-exo-trig-vinyl-3-exo-radical cyclization-rearrangement reaction and its allylic radical version was developed for the synthesis of DEF ring system of the nor-tritepene Pfaffic acid.

    Link :

    7. "Synthesis Based on Cyclohexadienes: Part 34. A Tandem Cationic Rearrangement-Ene Cyclisation Route to 2-Pupukeanone. P. J. Biju, Krishna P. Kaliappan, Laxmisha, M. S. and G. S. R. Subba Rao, J. Chem. Soc. Perkin Trans 1. 2000, 3714-3718.

    A new strategy for the construction of the isotwistane skeleton is reported from easily available cyclohexadienes, which involves a one-pot cationic skeletal rearrangement and ene cyclization of a bicyclo[2.2.2]octenone derivative and a cationic rearrangement of a tricyclo[5.3.0.0]decane to a [4.3.1.0]decane skeleton as the key steps in the synthesis of 2-pupukeanone.

    Link :

    6. "Synthesis Based on Cyclohexadienes: Part 24. A New Total Synthesis of 2-Pupukeanone and a Facile Entry to Copa and Ylanga Sesquiterpene Skeleton". Krishna P. Kaliappan and G. S. R. Subba Rao., J. Chem. Soc. Perkin Trans 1. 1997, 3393-3399.

    A novel tandem 5-exo-trigallyl and 3-exo-trigradical cyclization and rearrangement to copa and ylangatype sesquiterpene skeletons from easily prepared cyclohexadienes is reported. A new total synthesis ofpupukean-2-one, which belongs to a novel class of sesquiterpenes, involving a 5-exo-trigallyl radicalcyclisation as the key step is also reported.

    Link :

    5. "Synthesis Based on Cyclohexadienes: Part 23. Total Synthesis of 5-epi-2-Pupukeanone." Krishna P. Kaliappan and G. S. R. Subba Rao, J. Chem. Soc. Perkin. Trans. 1. 1997, 3387-3392.

    A new strategy for the construction of the isotwistane skeleton is reported from easily availablecyclohexadienes which involves stereoselective alkylation of a bicyclooctenone derivativeand adecarboxylative 5-exo-trigradical cyclisation as the key steps in the total synthesis of 5-epi-pupukean-2-one.

    Link :

    4. "Synthesis Based on Cyclohexadienes: Part 22. Formal Syntheses of Norpatchoulenol and Patchouli Alcohol." Krishna P. Kaliappan and G. S. R. Subba Rao, J. Chem. Soc. Perkin. Trans. 1., 1997, 1385-1389.

    The preparation of 6-endo-formyl-1,3,3-trimethylbicyclo[2.2.2]octan-2-one and 6-endo -acetyl-1,3,3-trimethylbicyclo[2.2.2]octan-2-one, the two key intermediates for the synthesis of patchouli alcohol and norpatchoulenol, is reported by a simple and short method from 2-methylbenzoic acid.

    Link :

    3. "A New Total Synthesis of 2-Pupukeanone." Krishna. P Kaliappan and G. S. R. Subba Rao, Tetrahedron Lett. 1997, 2185-2186.

    An efficient total synthesis of 2-pupukeanone is reported which involves a 5-exo-trig allyl radical cyclization as the key step to construct the isotwistane skeleton.

    Link :

    2. "An expedient route to the preparation of the key intermediates for the total synthesis of Aphidicolin, Stemodin and Oryzalexin S." Krishna P. Kaliappan and G. S. R. Subba Rao, Tetrahedron Lett. 1996, 8429-8430.

    A novel strategy for the construction of tricyclo[6.3.1.0]dodecane and tricyclo[7.2.1.0]dodecane carbon skeleton present in several complex diterpenes is described.

    Link :

    1. "Tandem 5-exo-trig allyl and 3-exo-trig cyclization and its rearrangement to Copa and Ylanga sesquiterpene skeleton." Krishna P. Kaliappan and G. S. R. Subba Rao, Chem. Commun. 1996, 2331-2332.

    A novel tandem 5-exo-trig allyl and 3-exo-trig radical cyclisation and rearrangement to copa and ylanga type sesquiterpene skeleton is reported.

    Link :