Scope and Mechanism of the Highly Stereoselective Metal-Mediated Domino Aldol Reactions of Enolates With Aldehydes

Beilstein Journal of Organic Chemistry - Germany
doi 10.3762/bjoc.12.80
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Beilstein Institut

Related search

Stereoselective Acetate Aldol Reactions From Metal Enolates

Synthesis
Organic ChemistryCatalysis
2011English

Highly Anti-Selective Catalytic Aldol Reactions of Amides With Aldehydes

English

One-Pot Organocatalytic Domino Michael-Aldol and Intramolecular SN2 Reactions. Asymmetric Synthesis of Highly Functionalized Epoxycyclohexanone Derivatives

English

Highly Stereoselective Oxidative Esterification of Aldehydes With B-Dicarbonyl Compounds

English

Highly Stereoselective Oxidative Esterification of Aldehydes With B-Dicarbonyl Compounds

English

The Supersilyl Group as a Carboxylic Acid Protecting Group: Application to Highly Stereoselective Aldol and Mannich Reactions

Angewandte Chemie - International Edition
CatalysisChemistry
2013English

Recent Developments in Enantioselective Metal-Catalyzed Domino Reactions

Advanced Synthesis and Catalysis
Organic ChemistryCatalysis
2019English

Highly Stereoselective TiCl4-Catalyzed Evans-Aldol and Et3Al-Mediated Reformatsky Reactions. Efficient Accesses to Optically Active Syn- Or Anti-A-Trifluoromethyl-B-Hydroxy Carboxylic Acid Derivatives

English

Gold(I)-Catalyzed Stereoselective Cyclization of 1,3-Enyne Aldehydes by 1,3-Acyloxy Migration/Nazarov/Aldol Cascade

2019English

Amanote Research

Note-taking for researchers

Follow Amanote

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

Privacy PolicyRefund Policy