Sangeeta V. Pitre
Purdue University West Lafayette(US)
Publications by Year
Research Areas
Chemical Synthesis and Reactions, Asymmetric Synthesis and Catalysis, Asymmetric Hydrogenation and Catalysis, Oxidative Organic Chemistry Reactions, Chemical Synthesis and Analysis
Most-Cited Works
- → Selective Reductions. 59. Effective Intramolecular Asymmetric Reductions of α-, β-, and γ-Keto Acids with Diisopinocampheylborane and Intermolecular Asymmetric Reductions of the Corresponding Esters with B-Chlorodiisopinocampheylborane(2002)55 cited
- → Efficient Intramolecular Asymmetric Reductions of α-, β-, and γ-Keto Acids with Diisopinocampheylborane1(2000)33 cited
- → Studies in Lewis acid and LiClO4 (or Nafion-H) catalysed ionic Diels-Alder reactions of chiral and achiral olefinic acetals respectively(1999)29 cited
- → Trimethylsilylnitrate−Chromium Trioxide and Trimethylsilylnitrate−DMSO: Novel Reagent Systems for One Step Conversion of Olefins into α-Nitro Ketones and Cyclic Ethers into Lactones1(1999)20 cited
- → Palladium catalysed conversion of vinyl bromo allylic alcohols into vinylic carbonyl compounds and oxidation of secondary alcohols to ketones(1996)16 cited
- → Zeolite (H-ZSM5) Catalysed Regioselective Isomerisation of Glycidic Esters to α-Hydroxy-β,γ-Unsaturated Esters1(1996)13 cited
- → Zeolite H-ZSM 5 Catalysed Oxidation of Alcohols with Chromium Trioxide. Part 9.1 General Synthetic Methods†(1997)12 cited
- → Acetoxyselenation of Olefins with Selenium Dioxide-acetic Anhydride Reagent System1(1997)5 cited
- → Selective Reductions. Part 59. Effective Intramolecular Asymmetric Reductions of α‐, β‐, and γ‐Keto Acids with Diisopinocampheylborane and Intermolecular Asymmetric Reductions of the Corresponding Esters with B‐Chlorodiisopinocampheylborane.(2003)2 cited
- → ChemInform Abstract: General Synthetic Methods. Part 6. Acetoxyselenation of Olefins with Selenium Dioxide‐Acetic Acid Anhydride Reagent System.(1997)1 cited