Complete list of publications

From University of Hyderabad

  1. Baylis-Hillman reaction: in situ generated isoquinolinium species as excellent electrophiles for coupling with alkyl acrylates and acrylonitrile
    D. Basavaiah, P. Thamizharasi Eur. J. Org. Chem. 2017, 5135-5140.
  2. Highly diastereoselective synthesis of tertiary alcohols via intramolecular Baylis-Hillman reaction using less reactive acrylamides as activated alkenes and ketones as electrophiles
    D. Basavaiah, G. C. Reddy, B. Lingaiah, R.T. Naganaboina Tetrahedron, 2017, 73, 859-867.
  3. Baylis–Hillman acetates in synthesis:Copper(I)/tert-butyl hydroperoxide promoted one-pot oxidative intramolecular cyclization protocol for the preparation of pyrrole-fused compounds and the formal synthesis of (±)-crispine A
    D. Basavaiah, B. Lingaiah, G. C. Reddy, B. C. Sahu Eur. J. Org. Chem. 2016, 2398-2403.
  4. Intramolecular Baylis-Hillman reaction: synthesis of heterocyclic molecules (JY-9322KR)
    D. Basavaiah, G. C. Reddy ARKIVOC 2016, 172 – 205.
  5. The Baylis-Hillman acetates as a source of ambiphilic molecules: a simple synthesis of 1,3-thiazinane-2-thione frameworks
    D. Basavaiah, S. Pal, G.Veeraraghavaiah, K. C. Bharadwaj Tetrahedron, 2015, 71, 4659-4664.
  6. Less reactive ketones as electrophiles and acrylamides as activated alkenes in intramolecular Baylis- Hillman reaction: facile synthesis of functionalized γ-lactam frameworks
    D. Basavaiah, G. C. Reddy, K. C. Bharadwaj Tetrahedron, 2014, 70, 7991-7995.
  7. The Baylis-Hillman acetates in organic synthesis: unprecedented sodium nitrite induced intramolecular Friedel-Crafts cyclization of secondary nitro compounds
    D. Basavaiah, D. M. Reddy RSC Adv. 2014, 4, 23966-23970.
  8. The acrylamide moiety as an activated alkene component in intramolecular Baylis-Hillman reaction: a facile synthesis of functionalized α-methylene lactam and spirolactam frameworks
    D. Basavaiah, G. C. Reddy, K. C. Bharadwaj Eur. J. Org. Chem. 2014, 1157-1162.
  9. Ketones as electrophiles in two component Baylis-Hillman reaction: a facile one-pot synthesis of substituted indolizines
    D. Basavaiah, G.Veeraraghavaiah, S. S. Badsara Org. Biomol. Chem. 2014, 12, 1551-1555.
  10. Synthesis of fused nine-membered rings: a simple protocol for synthesis of [1,2,3]-triazolo-[1,4]-benzoxazonine frameworks from the Baylis-Hillman acetates
    D. Basavaiah, B. S. Reddy, H. Lingam Tetrahedron, 2013, 69, 10060-10067.
  11. Baylis-Hillman carbonates in organic synthesis: a convenient one-pot strategy for nitrone-spiro-oxindole frameworks
    D. Basavaiah, S. S. Badsara, G.Veeraraghavaiah Tetrahedron, 2013, 69, 7995-8001.
  12. The Baylis–Hillman acetates in organic synthesis: development of a facile strategy for synthesis of functionalized unsaturated benzo-fused macrocyclic ethers and [n] metacyclophanes
    D. Basavaiah, K. S. Kumar, K. Aravindu, B. Lingaiah RSC Adv. 2013, 3, 9629-9632.
  13. Conceptual influence of the Baylis-Hillman reaction on recent trends in organic synthesis
    D. Basavaiah, B. C. Sahu Chimia 2013, 67, 8-16.
  14. Baylis-Hillman bromides as a source of 1,3-dipoles : sterically directed synthesis of oxindole fused spiro oxirane and dihydrofuran frameworks
    D. Basavaiah, S. S. Badsara, B. C. Sahu Chem. Eur. J. 2013, 19, 2961-2965.
  15. Baylis-Hillman acetates in carbocyclic synthesis : a convenient protocol for synthesis of densely substituted indenes
    D. Basavaiah, B. S. Reddy, H. Lingam Tetrahedron, 2013, 69, 1994-2003.
  16. Baylis-Hillman acetates in organic synthesis: convenient one-pot synthesis of α-carboline framework a concise synthesis of neocryptolepine
    D. Basavaiah, D. M. Reddy Org. Biomol. Chem. 2012, 10, 8774-8777.
  17. The Baylis-Hillman reaction: a novel concept for creativity in chemistry
    D. Basavaiah, G. Veeraraghavaiah Chem. Soc. Rev. 2012, 41, 68-78.
  18. Synthesis of substituted maleimide derivatives using the Baylis-Hillman adducts
    D. Basavaiah, D. V. Lenin, G. Veeraraghavaiah Curr. Sci. 2011, 101, 888-893.
  19. A facile synthesis of substituted indenones and piperidine-2,6-diones from the Baylis-Hillman acetates
    D. Basavaiah, D. V. Lenin Eur. J. Org. Chem. 2010, 5650-5658.
  20. Toward understanding the scope of Baylis-Hillman reaction: synthesis of 3-(2-hydroxyphenyl) indolin-2-ones and polycyclic fused furans
    D. Basavaiah, S. Roy, U. Das Tetrahedron, 2010, 66, 5612-5622.
  21. Recent contributions from the Baylis-Hillman reaction to organic chemistry
    D. Basavaiah, B. S. Reddy, S. S.Badsara Chem. Rev. 2010, 110, 5447-5674.
  22. Simple, one-pot and facile synthesis of angularly fused [6-7-5], [6-7-6], [6-7-7] and [6,7] ring systems using Baylis-Hillman acetates
    D. Basavaiah, K. Aravindu, K. S. Kumar, K. R. Reddy Eur. J. Org. Chem. 2010,1843-1848.
  23. The Baylis-Hillman adducts as valuable source for one-pot multi-step synthesis: a facile synthesis of substituted piperidin-2-ones
    D. Basavaiah, R. J. Reddy, D. V. Lenin Helv. Chim. Acta. 2010, 93, 1180-1186.
  24. Simple and one-pot synthesis of tri and tetracyclic frameworks containing [1,8]naphthyridin-2-one moiety from the Baylis-Hillman adducts
    D. Basavaiah, K. R. Reddy Tetrahedron, 2010, 66, 1215-1219.
  25. A facile one-pot transformation of the Baylis-Hillman adducts into unsymmetrical disubstituted maleimide and maleic anhydride frameworks: a facile synthesis of himanimide A
    D. Basavaiah, B. Devendar, K. Aravindu, A. Veerendhar Chem. Eur.J. 2010, 16, 2031-2035.
  26. Towards chiral diamines as chiral catalytic precursors for the borane-mediated enantioselective reduction of prochiral ketones
    D. Basavaiah, U. Das, S. Roy J. Chem. Sci. 2009, 121, 1003-1010.
  27. A simple protocol for the synthesis of a piperidine-2,6-dione framework from Baylis-Hillman adducts
    D. Basavaiah, D. V. Lenin, B. Devendar Tetrahedron Lett. 2009, 50, 3538–3542.
  28. The Baylis-Hillman bromides as versatile synthons: a facile one-pot synthesis of indolizine and benzofused indolizine frameworks
    D. Basavaiah, B. Devendar, D. V. Lenin, T. Satyanarayana Synlett, 2009, 411-416.
  29. Dimethyl sulfide induced [3+2] annulation strategy: an efficient synthesis of functionalized dihydropyrazole derivatives using the Baylis-Hillman bromides
    D. Basavaiah, S. Roy Org. Lett. 2008, 10, 1819-1822.
  30. Simple and facile synthesis of tetralone-spiro-glutarimides and spirobisglutarimides from the Baylis-Hillman acetates
    D. Basavaiah, R. J. Reddy Org. Biomol. Chem. 2008, 6, 1034-1039.
  31. An expedient, facile, and simple one-pot synthesis of 2-methylenealkanoates and alkanenitriles from the Baylis-Hillman bromides in aqueous media
    D. Basavaiah, K. R. Reddy, N. Kumaragurubaran Nature Protocols 2007, 2, 2665-2676.
  32. The Baylis-Hillman acetates as a valuable source for one-pot multistep synthesis: a facile synthesis of functionalized tri-/ tetracyclic frameworks containing azocine moiety
    D. Basavaiah, K. Aravindu Org. Lett. 2007, 9, 2453-2456.
  33. The Baylis-Hillman reaction: a novel source of attraction, opportunities, and challenges in synthetic chemistry
    D. Basavaiah, K. V. Rao, R. J. Reddy Chem. Soc. Rev. 2007, 36, 1581-1588.
  34. Chiral diamides as efficient catalytic precursors for the borane-mediated asymmetric reduction of prochiral ketones
    D. Basavaiah, K. V. Rao, B. S. Reddy Tetrahedron: Asymmetry 2007, 18, 968-974.
  35. (5S)-1-Aza-2-imino-3-oxa-4,4-diphenylbicyclo(3.3.0)octane: a novel chiral catalytic source containing the N-(C=NH)-O moiety for the borane-mediated asymmetric reduction of prochiral ketones
    D. Basavaiah, K. V. Rao, B. S. Reddy Tetrahedron: Asymmetry 2007, 18, 963-967.
  36. Simple and one pot protocol for synthesis of indene-spiro-oxindoles involving tandem Prins and Friedel-Crafts reactions
    D. Basavaiah, K. R. Reddy Org. Lett. 2007, 9, 57-60.
  37. Organo-base mediated Cannizzaro reaction
    D. Basavaiah, D. S. Sharada, A. Veerendhar Tetrahedron Lett. 2006, 47, 5771–5774.
  38. An efficient and rapid chalcogenide-Morita-Baylis-Hillman process promoted by TBDMSOTf and a thiolane
    J. S. Rao, J-F. Brière, P. Metzner, D. Basavaiah Tetrahedron Lett. 2006, 47, 3553-3556.
  39. (2S)-2-Anilinomethylpyrrolidine: an efficient in situ recyclable chiral catalytic source for the borane-mediated asymmetric reduction of prochiral ketones in refluxing toluene
    D. Basavaiah, K. V. Rao, B. S. Reddy Tetrahedron: Asymmetry 2006, 17,1041-1044.
  40. (5S)-1,3-Diaza-2-imino-3-phenylbicyclo(3.3.0)octane: first example of guanidine based in situ recyclable chiral catalytic source for borane-mediated asymmetric reduction of prochiral ketones
    D. Basavaiah, K. V. Rao, B. S. Reddy Tetrahedron: Asymmetry 2006, 17, 1036-1040.
  41. Applications of Baylis-Hillman adducts: a simple, convenient, and one-pot synthesis of 3-benzoyl-quinolines
    D. Basavaiah, R. J. Reddy, J. S. Rao Tetrahedron Lett. 2006, 47, 73-77.
  42. A study toward understanding the role of a phosphorus stereogenic center in (5S)-1,3-diaza-2- phospha-2-oxo-3-phenylbicyclo(3.3.0)octane derivatives as catalysts in the borane-mediated asymmetric reduction of prochiral ketones
    D. Basavaiah, V. Chandrashekar, U. Das, G. J. Reddy Tetrahedron: Asymmetry 2005, 16, 3955-3962.
  43. TiCl4 catalyzed tandem construction of C-C and C-O bonds: a simple and one-pot atom-economical stereoselective synthesis of spiro-oxindoles
    D. Basavaiah, J. S. Rao, R. J. Reddy, A. J. Rao Chem. Commun. 2005, 2621-2623.
  44. Simple, facile, and one-pot conversion of the Baylis-Hillman adducts into functionalized 1,2,3,4-tetrahydroacridines and cyclopenta[b]quinolines
    D. Basavaiah, J. S. Rao, R. J. Reddy J. Org. Chem. 2004, 69, 7379-7382.
  45. Toward effective chiral catalysts containing the N-P=O structural framework for the borane- mediated asymmetric reduction of prochiral ketones
    D. Basavaiah, G. J. Reddy, K. V.Rao Tetrahedron: Asymmetry 2004, 15, 1881-1888.
  46. A facile tandem construction of C-O and C-C bonds: a novel one-pot transformation of Baylis-Hillman adducts into 2-benzoxepines
    D. Basavaiah, D. S. Sharada, A. Veerendhar Tetrahedron Lett. 2004, 45, 3081-3083.
  47. Applications of Baylis-Hillman acetates: one-pot, facile and convenient synthesis of substituted γ-lactams
    D. Basavaiah, J. S. Rao Tetrahedron Lett. 2004, 45, 1621-1625.
  48. A novel, tandem construction of C-N and C-C bonds: facile and one-pot transformation of the Baylis-Hillman adducts into 2-benzazepines
    D. Basavaiah, T. Satyanarayana Chem. Commun. 2004, 32-33.
  49. A new chiral catalytic source with an N-P=O structural framework containing a proximal hydroxyl group for the borane-mediated asymmetric reduction of prochiral ketones
    D. Basavaiah, G. J. Reddy, V. Chandrashekar Tetrahedron: Asymmetry 2004, 15, 47-52.
  50. Steric factors direct Baylis–Hillman and aldol reactions in titanium tetrachloride mediated coupling between α-keto esters and cyclohex-2-enone derivatives
    D. Basavaiah, B. Sreenivasulu, A. J. Rao J. Org. Chem. 2003, 68, 5983-5991.
  51. 1-Benzopyran-4(4H)-ones as novel activated alkenes in the Baylis–Hillman reaction: a simple and facile synthesis of indolizine-fused-chromones
    D. Basavaiah, A. J. Rao Tetrahedron Lett. 2003, 44, 4365-4368.
  52. First example of electrophile induced Baylis-Hillman reaction: a novel facile one-pot synthesis of indolizine derivatives
    D. Basavaiah, A. J. Rao Chem. Commun. 2003, 604-605.
  53. Recent advances in the Baylis-Hillman reaction and applications
    D. Basavaiah, A. J. Rao, T. Satyanarayana Chem. Rev. 2003, 103, 811-891.
  54. Methanolic trimethylamine mediated Baylis-Hillman reaction
    D. Basavaiah, A. J. Rao, M. Krishnamacharyulu ARKIVOC 2002, VII, 136-145.
  55. The Baylis-Hillman reaction: one-pot facile synthesis of 2,4-functionalized 1,4-pentadienes
    D. Basavaiah, D. S. Sharada, N. Kumaragurubaran, R. M. Reddy J. Org. Chem. 2002, 67, 7135-7137.
  56. (2S,5S)-1,3-Diaza-2-phospha-2-oxo-2-chloro-3-phenylbicyclo(3.3.0)octane: a novel chiral source for borane-mediated catalytic chiral reductions
    D. Basavaiah, G. J. Reddy, V. Chandrashekar Tetrahedron: Asymmetry 2002, 13, 1125-1128.
  57. One-pot facile conversion of the acetates of Baylis-Hillman adducts into substituted fused pyrimidones in aqueous media
    D. Basavaiah, T. Satyanarayana Tetrahedron Lett. 2002, 43, 4301-4303.
  58. Applications of Baylis-Hillman chemistry: one-pot convenient synthesis of functionalized (1H)-quinol-2-ones and quinolines
    D. Basavaiah, R. M. Reddy, N. Kumaragurubaran, D. S. Sharada Tetrahedron 2002, 58, 3693-3697.
  59. Highly diastereoselective TiCl4 mediated addition of (E)-cinnamyl(tributyl)tin to α-keto esters
    D. Basavaiah, B. Sreenivasulu Tetrahedron Lett. 2002, 43, 2987-2990.
  60. Tandem construction of carbon-carbon and carbon-oxygen bonds in the Baylis-Hillman chemistry: synthesis of functionalized dl-bis allyl ethers
    D. Basavaiah, M. Bakthadoss, G. J. Reddy Synth. Commun. 2002, 32, 689-697.
  61. Novel titanium (IV) chloride catalyzed olefination of aldehydes: a simple and convenient synthesis of trans-cinnamic acids
    D. Basavaiah, A. J. Rao Synth. Commun. 2002, 32, 195-201.
  62. Applications of liver acetone powders in enantioselective synthesis
    D. Basavaiah ARKIVOC 2001, VIII, 70-82 [issue in honor of Prof. T. Govindachari].
  63. A novel and facile synthesis of functionalized [4.4.3] and [4.4.4]propellano-bislactones using acetates of the Baylis-Hillman adducts
    D. Basavaiah, T. Satyanarayana Org. Lett. 2001, 3, 3619-3622.
  64. Applications of Baylis-Hillman chemistry: enantioselective synthesis of (-)-methyl 3-aryl-2-methylene-3-(prop-2-yn-1-yloxy)propanoates via chiral leaving group strategy
    D. Basavaiah, N. Kumaragurubaran, D. S. Sharada, R. M. Reddy Tetrahedron 2001, 57, 8167-8172.
  65. Baylis-Hillman chemistry: a convenient stereoselective synthesis of (Z, Z)- & (E, E)-1,4-diallyl-piperazines
    D. Basavaiah, R. M. Reddy J. Chem. Res. (S) 2001, 354-355.
  66. The Baylis-Hillman reaction: rate acceleration in silica gel solid phase medium
    D. Basavaiah, R. M. Reddy Indian J. Chem. 2001, 40B, 985-988.
  67. One-pot inter- and intramolecular Friedel-Crafts reactions in Baylis-Hillman chemistry: a novel facile synthesis of (E)-2-arylideneindan-1-ones
    D. Basavaiah, R. M. Reddy Tetrahedron Lett. 2001, 42, 3025-3027.
  68. The Baylis-Hillman reaction: TiCl4 mediated coupling of alkyl vinyl ketones with α-keto esters and aldehydes
    D. Basavaiah, B. Sreenivasulu, R. M. Reddy, K. Muthukumaran Synth. Commun. 2001, 31, 2987-2995.
  69. A novel and effective chiral phosphoramide catalyst for the borane-mediated asymmetric reduction of prochiral α-halo ketones
    D. Basavaiah, G. J. Reddy, V. Chandrashekar Tetrahedron: Asymmetry 2001, 12, 685-689.
  70. The first intramolecular Friedel-Crafts reaction of Baylis-Hillman adducts: synthesis of functionalized indene and indane derivatives
    D. Basavaiah, M. Bakthadoss, G. J. Reddy Synthesis 2001, 919-923.
  71. A novel Baylis-Hillman protocol for the synthesis of functionalized fused furans
    D. Basavaiah, B. Sreenivasulu, J. S. Rao Tetrahedron Lett. 2001, 42, 1147-1149.
  72. The Baylis-Hillman chemistry in aqueous media: a convenient synthesis of 2-methylenealkanoates and alkanenitriles
    D. Basavaiah, N. Kumaragurubaran Tetrahedron Lett. 2001, 42, 477-479.
  73. Baylis-Hillman chemistry: a novel synthesis of functionalized 1,4-pentadienes
    D. Basavaiah, N. Kumaragurubaran, D. S. Sharada Tetrahedron Lett. 2001, 42, 85-87.
  74. The Baylis-Hillman reaction: one-pot stereoselective synthesis of methyl (2E)-3-aryl-2-hydroxy- methylprop-2-enoates
    D. Basavaiah, K. Padmaja, T. Satyanarayana Synthesis 2000, 1662-1664.
  75. Synthetic applications of the Baylis-Hillman adducts: a simple stereoselective synthesis of (E)-3-(nitroxymethyl)alk-3-en-2-ones
    D. Basavaiah, R. S. Hyma, N. Kumaragurubaran Tetrahedron 2000, 56, 5905-5907.
  76. The aqueous trimethylamine mediated Baylis-Hillman reaction
    D. Basavaiah, M. Krishnamacharyulu, A. J. Rao Synth. Commun. 2000, 30, 2061-2069.
  77. TMSOTf-catalyzed stereoselective isomerization of acetates of the Baylis-Hillman adducts
    D. Basavaiah, K. Muthukumaran, B. Sreenivasulu Synthesis 2000, 545-548.
  78. Stereoselective transformation of Baylis-Hillman adducts into (3E)-3-(alkoxymethyl)alk-3-en-2- ones
    D. Basavaiah, R. S. Hyma, K. Muthukumaran, N. Kumaragurubaran Synthesis 2000, 217-219.
  79. Applications of the Baylis-Hillman adducts in organic synthesis: a facile synthesis of [E]-α-cyano-cinnamyl alcohols and [E]-α-cyanocinnamic aldehydes
    D. Basavaiah, N. Kumaragurubaran, K. Padmaja Synlett 1999, 1630-1632.
  80. α-Keto esters as electrophiles for the chalcogeno-Baylis-Hillman reaction
    D. Basavaiah, K. Muthukumaran, B. Sreenivasulu Synlett 1999, 1249-1250.
  81. The Baylis-Hillman Reaction: an expedient synthesis of (Z)-keto allyl bromides and chlorides
    D. Basavaiah, R. S. Hyma, K. Padmaja, M. Krishnamacharyulu Tetrahedron 1999, 55, 6971-6976.
  82. A facile one-pot conversion of the acetates of the Baylis-Hillman adducts to [E]-α-methylcinnamic acids
    D. Basavaiah, M. Krishnamacharyulu, R. S. Hyma, P. K. S. Sarma, N. Kumaragurubaran J. Org. Chem. 1999, 64, 1197-1200.
  83. RuCl2(PPh3)3 catalyzed isomerization of the Baylis-Hillman adducts
    D. Basavaiah, K. Muthukumaran Synth. Commun. 1999, 29, 713-719.
  84. A new protocol for the synthesis of [E]- 3-benzylidenechroman-4-ones: a simple synthesis of the methyl ether of bonducellin
    D. Basavaiah, M. Bakthadoss, S. Pandiaraju Chem. Commun. 1998, 1639-1640.
  85. Arylation of the Baylis-Hillman adducts
    D. Basavaiah, K. Muthukumaran Tetrahedron 1998, 54, 4943-4948.
  86. The Friedel-Crafts reaction of the Baylis-Hillman adducts
    D. Basavaiah, M. Krishnamacharyulu, R. S. Hyma, S. Pandiaraju Tetrahedron Lett. 1997, 38, 2141-2144.
  87. Unprecedented stereochemical reversal from alkyl to aryl substituents in the Johnson-Claisen rearrangement of methyl 3-hydroxy-2-methylenealkanoates
    D. Basavaiah, S. Pandiaraju, M. Krishnamacharyulu Synlett 1996, 747-748.
  88. The Friedel-Crafts chemistry: acetates of the Baylis-Hillman adducts as novel stereodefined β- electrophiles
    D. Basavaiah, S. Pandiaraju, K. Padmaja Synlett 1996, 393-395.
  89. The Baylis-Hillman reaction: a novel carbon-carbon bond forming reaction
    D. Basavaiah, P. D. Rao, R. S. Hyma Tetrahedron 1996, 52, 8001-8062.
  90. (1R,2R)-2-Nitroxycyclohexan-1-ol: first example of a cyclohexyl-based chiral auxiliary with nitroxy function as diastereoface discriminating group
    D. Basavaiah, S. Pandiaraju, M. Bakthadoss, K. Muthukumaran Tetrahedron: Asymmetry 1996, 7, 997-1000.
  91. Enantioselective synthesis of (1R, 2R)- and (1S, 2S)-2-nitroxycyclohexan-1-ols
    D. Basavaiah, S. Pandiaraju, K. Muthukumaran Tetrahedron: Asymmetry 1996, 7, 13-16.
  92. Nucleophilic addition of triethyl phosphite to acetates of the Baylis-Hillman adducts: stereoselective synthesis of (E)- and (Z)-allylphosphonates
    D. Basavaiah, S. Pandiaraju Tetrahedron 1996, 52, 2261-2268.
  93. Synthetic applications of the Baylis-Hillman reaction: simple synthesis of [2E]-2-butyloct-2-enal and [2E]-2-tridecylheptadec-2-enal
    D. Basavaiah, R. S. Hyma Tetrahedron 1996, 52, 1253-1258.
  94. New cyclohexyl-based chiral auxiliaries: enantioselective synthesis of α-hydroxy acids.
    D. Basavaiah, P. Rama Krishna Tetrahedron 1995, 51, 12169-12178.
  95. Enantioselective hydrolysis of 2,2-disubstituted oxiranes mediated by microsomal epoxide- hydrolase
    D. Basavaiah, S. B. Raju Synth. Commun. 1995, 25, 3293-3306.
  96. Synthesis of enantiomerically enriched anti-homoallyl alcohols mediated by crude chicken liver esterase (CCLE)
    D. Basavaiah, P. D. Rao Tetrahedron: Asymmetry 1995, 6, 789-800.
  97. The Baylis-Hillman reaction: a novel method for the synthesis of α-methylidene-β-hydroxyketonesand 2-methylidene-1,5-diketones
    D. Basavaiah, V. V. L. Gowriswari, P. D. Rao, T. K. Bharathi J. Chem. Res.(S).1995, 267.
  98. Synthesis of chiral α-aryl-α-hydroxyacetic acids: substituent effects in pig liver acetone powder (PLAP) induced enantioselective hydrolysis
    D. Basavaiah, P. Rama Krishna Tetrahedron 1995, 51, 2403-2416.
  99. A convenient enantioselective synthesis of trans-2-aryloxycyclohexan-1-ols using pig liver acetone powder (PLAP) as biocatalyst
    D. Basavaiah, P. Rama Krishna, T. K. Bharathi Tetrahedron: Asymmetry 1995, 6, 439-454.
  100. The Johnson-Claisen rearrangement of 3-hydroxy-2-methylenealkanenitriles: stereoselective synthesis of functionalized trisubstituted alkenes
    D. Basavaiah, S. Pandiaraju Tetrahedron Lett. 1995, 36, 757-758.
  101. Baylis-Hillman reaction: magnesium bromide as a stereoselective reagent for the synthesis of [E]- and [Z]-allylbromides
    D. Basavaiah, A. K. D. Bhavani, S. Pandiaraju, P. K. S. Sarma Synlett 1995, 243-244.
  102. Pig liver acetone powder (PLAP) mediated enantioselective synthesis of cyclic ketones
    D. Basavaiah, P. Rama Krishna Synth. Commun. 1995, 25, 277-282.
  103. Pig liver acetone powder (PLAP) as biocatalyst: enantioselective synthesis of trans-2-alkoxy-cyclohexan-1-ols
    D. Basavaiah, P. Rama Krishna Tetrahedron 1994, 50, 10521-10530.
  104. (1R,2R)-2-Phenoxycyclohexan-1-ol as chiral auxiliary: enantioselective synthesis of frontalin
    D. Basavaiah, T. K. Bharathi, P. Rama Krishna J. Indian Inst. Sci. 1994, 74, 227-230.
  105. First enantioselective synthesis of mikanecic acid via Diels-Alder cycloaddition mediated construction of chiral vinylic quaternary center
    D. Basavaiah, S. Pandiaraju, P. K. S. Sarma Tetrahedron Lett. 1994, 35, 4227-4230.
  106. Bovine liver acetone powder (BLAP) catalyzed synthesis of chiral C-8 allyl alcohols: an application of substrate specificity approach
    D. Basavaiah, S. B. Raju Tetrahedron 1994, 50, 4137-4148.
  107. Enzymatic resolution of trans-2-arylcyclohexan-1-ols using crude chicken liver esterase (CCLE) as biocatalyst
    D. Basavaiah, P. D. Rao Tetrahedron: Asymmetry 1994, 5, 223-234.
  108. Crude chicken liver esterase mediated resolution of homo allyl alcohols
    D. Basavaiah, P. D. Rao Synth. Commun. 1994, 24, 925-929.
  109. Biocatalytic approach to optically active Baylis-Hillman reaction products
    D. Basavaiah, P. D. Rao Synth. Commun. 1994, 24, 917-923.
  110. Applications of the Baylis-Hillman reaction 2. a simple stereoselective synthesis of [E]- and [Z]- trisubstituted alkenes
    D. Basavaiah, P. K. S. Sarma, A. K. D. Bhavani J. Chem. Soc., Chem. Commun. 1994, 1091-1092.
  111. Selective enzymatic hydrolysis of phenolic acetates
    D. Basavaiah, S. B. Raju Synth. Commun. 1994, 24, 467-473.
  112. Enantioselective synthesis using crude enzymes
    D. Basavaiah, P. Rama Krishna Indian J. Chem. 1993, 32B, 131-134.
  113. Bovine liver acetone powder (BLAP): a crude enzyme for synthesis of optically active 1-aryl-1-alkanols
    D. Basavaiah, S. B. Raju Bioorg. & Med. Chem. Lett.1992, 2, 955-958.
  114. Applications of Baylis-Hillman coupling products: a remarkable reversal of stereochemistry from esters to nitriles. a simple synthesis of [2E]-2-methylalk-2-en-1-ols and [2Z]-2-methylalk-2- enenitriles
    D. Basavaiah, P. K. S. Sarma J. Chem. Soc., Chem. Commun. 1992, 955-957.
  115. Enantioselective synthesis using crude enzymes
    D. Basavaiah, P. Rama Krishna Pure and Appl. Chem. 1992, 64, 1067-1072.
  116. trans-2-Phenoxycyclohexan-1-ol as a new chiral auxiliary: synthesis of chiral α-hydroxy acids
    D. Basavaiah, T. K. Bharathi, P. Rama Krishna Synth. Commun. 1992, 22, 941-947.
  117. Synthesis of chiral 1-arylalkan-1-ols using crude enzymes
    D. Basavaiah, S. B. Raju Synth. Commun. 1991, 21, 1859-1863.
  118. Enantioselective synthesis of α- and β-hydroxy acids using trans-2-phenylcyclohexan-1-ol as chiral auxiliary
    D. Basavaiah, T. K. Bharathi Tetrahedron Lett. 1991, 32, 3417-3420.
  119. Convenient enantioselective hydrolysis of racemic trans-1-acetoxy-2-aryloxycyclohexanes by crude pig liver acetone powder (PLAP)
    D. Basavaiah, P. Rama Krishna, T. K. Bharathi Tetrahedron Lett. 1990, 31, 4347-4348.
  120. Enantioselective hydrolysis of racemic acetates of homoallyl alcohols by crude pig liver acetone powder (PLAP)
    D. Basavaiah, P. D. Rao, Synth. Commun. 1990, 20, 2945-2949.
  121. Terminal hydroxyalkyl acrylates as substrates for Baylis-Hillman reaction
    D. Basavaiah, P. K. S. Sarma Synth. Commun. 1990, 20, 1611-1615.
  122. Chiral acrylates as substrates in Baylis-Hillman reaction
    D. Basavaiah, V. V. L. Gowriswari, P. K. S. Sarma, P. D. Rao Tetrahedron Lett. 1990, 31, 1621-1624.
  123. Towards chiral Reformatsky reagents
    D. Basavaiah, T. K. Bharathi Synth. Commun. 1989, 19, 2035-2039.
  124. Diethyl ketomalonate: a fast reacting substrate for Baylis-Hillman reaction
    D. Basavaiah, V. V. L. Gowriswari Synth. Commun. 1989, 19, 2461-2465.
  125. Sulfuric acid catalyzed decarbonylation of alkoxyacetyl chlorides
    D. Basavaiah, P. D. Rao, V. V. L. Gowriswari Synth. Commun. 1988, 18, 1411-1414.
  126. DABCO catalyzed dimerization of α,β-unsaturated ketones and nitriles
    D. Basavaiah, V. V. L. Gowriswari, T. K. Bharathi Tetrahedron Lett. 1987, 28, 4591-4592.
  127. DABCO catalyzed coupling of α-keto esters with acrylonitrile and methyl acrylate
    D. Basavaiah, T. K. Bharathi, V. V. L. Gowriswari Tetrahedron Lett. 1987, 28, 4351-4352.
  128. A general synthesis of α-methylene-β-hydroxyalkanones
    D. Basavaiah, T. K. Bharathi, V. V. L. Gowriswari Synth. Commun. 1987, 17, 1893-1896.
  129. A simple synthesis of 2-(1-hydroxyalkyl)acrylonitriles
    D. Basavaiah, V. V. L. Gowriswari Synth. Commun. 1987, 17, 587-591.
  130. A simple synthesis of α-methylene-β-hydroxyalkanones
    D. Basavaiah, V. V. L. Gowriswari Tetrahedron Lett. 1986, 27, 2031-2032.

    From the Purdue University

  131. Pheromone synthesis via organoboranes. 3. vinylic organoboranes. 10. stereospecific synthesis of [Z]- and [E]-6- and 7-alken-1-ols via boracyclanes
    H. C. Brown, D. Basavaiah, S. M. Singh, N. G. Bhat J. Org. Chem. 1988, 53, 246-250.
  132. Vinylic organoboranes. 9. a general stereospecific synthesis of [Z]- and [E]-disubstituted alkenes via organoboranes
    H. C. Brown, D. Basavaiah, S. U. Kulkarni, N. G. Bhat, J. V. N. V. Prasad J. Org. Chem. 1988, 53, 239-246.
  133. Vinylic organoboranes. 6. a general synthesis of [E]-disubstituted alkenes or ketones via the [E]- (1-substituted-1-alkenyl)boronic esters
    H. C. Brown, D. Basavaiah, S. U. Kulkarni, H. D. Lee, E. Negishi, J. J. Katz J. Org. Chem. 1986, 51, 5270-5276.
  134. Vinylic organoboranes. 4. a general, one-pot synthesis of 6- and 7-alkyn-1-ols via boracyclanes. Influence of steric effects in the iodination of lithium alkynyl “ate” complexes of dialkylborinates
    H. C. Brown, D. Basavaiah, N. G. Bhat J. Org. Chem. 1986, 51, 4518-4521.
  135. Pheromone synthesis via organoboranes: a stereoselective synthesis of [E]-1,3-alkenynes via thexylchloroborane-dimethyl sulfide
    H. C. Brown, N. G. Bhat, D. Basavaiah Synthesis 1986, 674-676.
  136. Pheromone synthesis via organoboranes: a general one-pot synthesis of [E]-6-alken-1-ols
    H. C. Brown, D. Basavaiah, S. M. Singh Synthesis 1984, 920-922.
  137. Pheromone synthesis via organoboranes: a simple synthesis of [Z]-5-undecen-2-one, a ketone fromthe pedal gland of the bontebok (Damaliscus dorcas dorcas)
    H. C. Brown, U. S. Racherla, D. Basavaiah Synthesis 1984, 303-304.
  138. Organoboranes. 36. a simple, general synthesis of alkynyl ketones and [E]-1,3-alkenynes via thexylchloroborane-dimethyl sulfide
    H. C. Brown, N. G. Bhat, D. Basavaiah Israel J. Chem. 1984, 24, 72-75.
  139. General synthesis of alkylalkenylalkynylboranes via haloboranes
    H. C. Brown, D. Basavaiah, N. G. Bhat Organometallics 1983, 2, 1468-1470.
  140. Organoboranes. 29. A convenient synthesis of alkyldibromoboranes and dialkylbromoboranes via hydroboration-redistribution
    H.C. Brown, D. Basavaiah, N. G. Bhat Organometallics 1983, 2, 1309-1311
  141. Synthetic applications of organoboranes: a simple synthesis of dihydrojasmone
    H. C. Brown, D. Basavaiah, U. S. Racherla Synthesis 1983, 886-888.
  142. A simple synthesis of alkynyl ketones via thexylchloroborane
    H. C. Brown, N. G. Bhat, D. Basavaiah Synthesis 1983, 885-886.
  143. Pheromone synthesis via organoboranes: a convenient stereospecific synthesis of racemic disparlure the sex pheromone of the gypsy moth (porthetria dispar L)
    H. C. Brown, D. Basavaiah Synthesis 1983, 283-284.
  144. General stereospecific synthesis of trisubstituted alkenes via step-wise hydroboration
    H. C. Brown, D. Basavaiah J. Org. Chem. 1982, 47, 5407-5409.
  145. A general and stereospecific synthesis of trans alkenes and regiospecific synthesis of ketones via stepwise hydroboration
    H. C. Brown, D. Basavaiah, S. U. Kulkarni J. Org. Chem. 1982, 47, 3808-3810.
  146. A general and stereospecific synthesis of cis alkenes via step-wise hydroboration: A simple synthesis of muscalure, the sex pheromone of the housefly (Musca domestica)
    H. C. Brown, D. Basavaiah J. Org. Chem. 1982, 47, 3806-3808.
  147. Pheromone synthesis via organoboranes: a stereospecific synthesis of [Z]-7-alken-1-ols
    D. Basavaiah, H. C. Brown J. Org. Chem. 1982, 47, 1792-1793.
  148. A general synthesis of B-[cis-1-bromo-1-alkenyl]dialkylboranes: valuable intermediates for the synthesis of ketones, trans-alkenes and trisubstituted alkenes
    H. C. Brown, D. Basavaiah J. Org. Chem. 1982, 47, 754-756.
  149. A stereospecific synthesis of trisubstituted alkenes via hydridation of dialkylhaloboranes followed by hydroboration-iodination of internal alkynes
    H. C. Brown, D. Basavaiah, S. U. Kulkarni J. Org. Chem. 1982, 47, 171-173.
  150. Rational synthesis of mixed dialkylhaloboranes [RA RB BX] and mixed trialkylboranes [RA RB RCB] via step-wise hydridation-hydroboration of alkyldihaloboranes
    S. U. Kulkarni, D. Basavaiah, M. Zaidlewicz, H. C. Brown Organometallics 1982, 1, 212-214.
  151. Iodine-induced transfer of dialkylvinylboranes produced by the hydridation of dialkylhaloboranes in the presence of 1-alkynes. generalization of the Zweifel cis alkene synthesis
    S. U. Kulkarni, D. Basavaiah, H. C. Brown J. Organometal. Chem. 1982, 225, C1-C5.
  152. Hydroboration 58. monohydroboration of alkynes with representative dialkylboranes of varying steric requirements. a general synthesis of dialkylvinylboranes
    H. C. Brown, D. Basavaiah, S. U. Kulkarni J. Organometal. Chem. 1982, 225, 63-69.
  153. Pheromone synthesis via organoboranes: a stereospecific synthesis of [E]-7-alken-1-ols
    D. Basavaiah Heterocycles 1982, 18, 153-156.