WebFeb 1, 2016 · Remarkable progress in the enantioselective addition of Grignard reagents to carbonyl compounds has been made over the past decade. This enantioselective … WebDec 18, 2024 · The development and characterization of enantioselective catalytic kinetic resolution of allylic alcohols through asymmetric isomerization with chiral BINOL derivatives-based alkoxides as bifunctional Brønsted base catalysts were described in the study. A number of chiral BINOL derivatives-based alkoxides were synthesized, and …
Kinetic Resolution of Allylic Alcohol with Chiral BINOL-Based …
WebNov 30, 2011 · A mixture of alcohol (2 mmol), either acetic acid or trifluoroacetic acid (3 mmol, iodine (0.06 mmol), and anh. Na 2 SO 4 (0.02 mmol)) were stirred at 100°C for 48 h in a 3 mL amber screw-cap vial. The reaction product was dissolved in 1 mL dichloromethane, filtered and analysed by both GC/MS and chiral phase GC analysis as … WebFeb 14, 2024 · A study aimed at the synthesis and structure optimization of new, efficient, optically active β-amino alcohol ligands with a structure suitable for immobilization on … fites 2016
Corey–Itsuno reduction - Wikipedia
WebChiral alcohol compounds are widely used in the fields of organic synthesis, material science, medicine, agricultural chemistry and fine chemicals. Research applications (1) … WebJun 1, 2024 · The asymmetric O-alkylation of alcohols is a useful route to chiral ethers, but aliphatic secondary alcohols have proven to be difficult substrates. Here the authors report a method to achieve ... WebThe Corey–Itsuno reduction, also known as the Corey–Bakshi–Shibata (CBS) reduction, is a chemical reaction in which an achiral ketone is enantioselectively reduced to produce the corresponding chiral, non-racemic alcohol.The oxazaborolidine reagent which mediates the enantioselective reduction of ketones was previously developed by the laboratory of … fitesa nonwovens inc