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Records 121 to 136 of 136
| Authors | Title | Journal | Year | Vol. |
Issue | Pages |
| 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 |