Asymmetric [2,3]-Wittig Rearrangement Involving a Chiral Ester Enolate Terminus. A Chiral Synthesis Oferythro-Α-Hydroxy-Β-Alkyl Carboxylic Acid Derivatives

Chemistry Letters - Japan
doi 10.1246/cl.1987.69
Full Text
Abstract

Available in full text

Categories
Chemistry
Date
Authors
Publisher

The Chemical Society of Japan

Related search

Highly Regio- And Stereoselective Asymmetric Bromoazidation of Chiral A, B-Unsaturated Carboxylic Acid Derivatives: Scope and Limitations

English

Α,β-Unsaturated Carboxylic Acid Derivatives. VI. New Synthesis ofN-Acyl-α-dehydroamino Acid Esters

Bulletin of the Chemical Society of Japan
Chemistry
1974English

Asymmetric Synthesis of Α-Unsubstituted Β-Hydroxy Acids

2013English

Unexpected Catalytic Behavior of Chiral Bisoxazoline in Asymmetric Reaction of Lithium Ester Enolate With Imine.

Chemical and Pharmaceutical Bulletin
MedicineDrug DiscoveryChemistry
1999English

Recyclable Fluorous Cinchona Alkaloid Ester as a Chiral Promoter for Asymmetric Fluorination of Β-Ketoesters

Beilstein Journal of Organic Chemistry
Organic Chemistry
2012English

Enantioselective Conjugate Addition of a Lithium Ester Enolate Catalyzed by Chiral Lithium Amides

English

Chiral Amides in Asymmetric Synthesis

Pure and Applied Chemistry
ChemistryChemical Engineering
1992English

Organocatalytic Asymmetric Wittig Reactions: Generation of Enantioenriched Axially Chiral Olefins Breaking a Symmetry Plane

Synlett
Organic Chemistry
2011English

A Convenient Enantioselective Decarboxylative Aldol Reaction to Access Chiral Α-Hydroxy Esters Using Β-Keto Acids

Beilstein Journal of Organic Chemistry
Organic Chemistry
2014English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy