Design of a Nonreductive Method for Chemoselective Cleavage of Hydrazines in the Presence of Unsaturations: Application to a Stereoconvergent Three-Component Synthesis of (−)-Methyl Palustramate-Reference-Cited by-同舟云学术

Design of a Nonreductive Method for Chemoselective Cleavage of Hydrazines in the Presence of Unsaturations: Application to a Stereoconvergent Three-Component Synthesis of (−)-Methyl Palustramate

Published:2004-11-01 Issue:24 Volume:69 Page:8429-8436
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Touré Barry B.¹,Hall Dennis G.¹

Affiliation:

1. Department of Chemistry, Gunning-Lemieux Chemistry Centre, University of Alberta, Edmonton, Alberta, T6G 2G2, Canada

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo048581o

Reference34 articles.

1. Diels-Alder reactions of 1,3-dienylboronates as a new route to functionalized carbocycles.

2. An improvement to the Vaultier tandem sequence: A practical highly stereoselective three-component reaction

3. Tandem Aza[4 + 2]/Allylboration: A Novel Multicomponent Reaction for the Stereocontrolled Synthesis of α-Hydroxyalkyl Piperidine Derivatives

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