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Ramachandran P. V.;Brown, H. C.;Swaminathan, S. Lithium-B-Iso-2-Ethylapopinocampheyl-9-Borabicyclo 3.3.1 Nonyl Hydride as an Improved Reagent for Asymmetric Reduction of Unhindered Aliphatic-Ketones - Further Evidence for the Improved Enantioselectivity in Reductions by Reagents Containing Increased S Tetrahedron: Asymmetry 1990 1 - 433-436
Brown H. C.;Srebnik, M.;Ramachandran, P. V. Chiral Synthesis Via Organoboranes .22. Selective Reductions .44. The Effect of the Steric Requirements of the Alkyl Substituent in Isopinocampheylalkylchloroboranes for the Asymmetric Reduction of Representative Ketones J. Org. Chem. 1989 54 - 1577-1583
Srebnik M.;Cole, T. E.;Ramachandran, P. V.;Brown, H. C. Hydroboration .84. Controlled and Sequential Hydroboration of Simple Representative Alkenes with Monoorganylboranes in Tetrahydrofuran - a Convenient Synthesis of Mixed Borinic Esters, R1r2bor3, and Mixed Trialkylboranes, R1r2r3b - an Examination of Posi J. Org. Chem. 1989 54 - 6085-6096
Brown H. C.;Ramachandran, P. V. Selective Reductions .45. Asymmetric Reduction of Prochiral Ketones by Iso-2-Methyl 2-(Benzyloxy)Ethyl Apopinocampheyl -Tert-Butylchloroborane, Iso-2-Ethyl 2-(Benzyloxy)Ethyl Apopinocampheyl -Tert-Butylchloroborane, and Iso-2- 2-(Benzyloxy)Ethyl Apopinoc J. Org. Chem. 1989 54 - 4504-4511
Brown H. C.;Chandrasekharan, J.;Ramachandran, P. V. Chiral Synthesis Via Organoboranes .14. Selective Reductions .41. Diisopinocampheylchloroborane, an Exceptionally Efficient Chiral Reducing Agent J. Am. Chem. Soc. 1988 110 - 1539-1546
Srebnik M.;Ramachandran, P. V.;Brown, H. C. Chiral Synthesis Via Organoboranes .18. Selective Reductions .43. Diisopinocampheylchloroborane as an Excellent Chiral Reducing Reagent for the Synthesis of Halo Alcohols of High Enantiomeric Purity - a Highly Enantioselective Synthesis of Both Optical I J. Org. Chem. 1988 53 - 2916-2920
Oberlender R.;Nichols, D. E.;Ramachandran, P. V.;Srebnik, M. Tomoxetine and the Stereoselectivity of Drug-Action J. Pharm. Pharmacol. 1987 39 - 1055-1056
Brown H. C.;Park, W. S.;Cho, B. T.;Ramachandran, P. V. Selective Reductions .40. A Critical-Examination of the Relative Effectiveness of Various Reducing Agents for the Asymmetric Reduction of Different Classes of Ketones J. Org. Chem. 1987 52 - 5406-5412
Brown H. C.;Chandrasekharan, J.;Ramachandran, P. V. Highly Efficient Asymmetric Reduction of Alpha-Tertiary Alkyl Ketones with Diisopinocampheylchloroborane J. Org. Chem. 1986 51 - 3394-3396
Brown H. C.;Ramachandran, P. V.;Chandrasekharan, J. Organoboranes .47. An Extremely Facile Elimination of Alkenes from Dialkylhaloboranes - a Comparative Rate Study with Related Trialkylboranes Organometallics 1986 5 - 2138-2141
Brown H. C.;Ramachandran, P. V.;Prasad, Jvnv Hydroboration .73. Relative Rates of Hydroboration of Representative Heterocyclic Olefins with 9-Borabicyclo 3.3.1 Nonane J. Org. Chem. 1985 50 - 5583-5586
Chandrasekharan J.;Ramachandran, P. V.;Brown, H. C. Diisopinocampheylchloroborane, a Remarkably Efficient Chiral Reducing Agent for Aromatic Prochiral Ketones J. Org. Chem. 1985 50 - 5446-5448
Ranganathan D.;Bamezai, S.;Ramachandran, P. V. A Study of the Preparation and Reactions of the Unusually Labile 5-Methyl 1,2,4 Oxadiazolo 2,3-C Quinazolin-2-One Heterocycles 1985 23 - 623-632
Ranganathan S.;Ranganathan, D.;Ramachandran, P. V. Iodoxybenzene - a Remarkably Close Ozone Equivalent Tetrahedron 1984 40 - 3145-3151
Ranganathan D.;Ranganathan, S.;Bamezai, S.;Mehrotra, S.;Ramachandran, P. V. 2-Nitroethyl Phenyl Sulfoxide - a Novel Reagent for Facile Nitroethylene Transfer J. Chem. Res.-S 1983 - - 78-79
Ranganathan S.;Ranganathan, D.;Ramachandran, P. V.;Mahanty, M. K.;Bamezai, S. A Chemical and Thermochemical Study of Non-Observed Symmetry Allowed Reactions Tetrahedron 1981 37 - 4171-4184