Toward the Development of a General Chiral Auxiliary. 5. High Diastereofacial Selectivity in Cycloadditions with Trienol Silyl Ethers: An Application to an Enantioselective Synthesis of (−)-Cassioside-Reference-Cited by-同舟云学术

Toward the Development of a General Chiral Auxiliary. 5. High Diastereofacial Selectivity in Cycloadditions with Trienol Silyl Ethers: An Application to an Enantioselective Synthesis of (−)-Cassioside

Published:1996-11-15 Issue:23 Volume:61 Page:7984-7985
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Boeckman Robert K.¹,Liu Yugang¹

Affiliation:

1. Department of Chemistry, University of Rochester, Rochester, New York 14627-0216

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo961613q

Reference21 articles.

1. Toward the Development of a General Chiral Auxiliary. 3. Design and Evaluation of a Novel Chiral Bicyclic Lactam for Asymmetric Aldol Condensations: Evidence for the Importance of Dipole Alignment in the Transition State

2. Toward the development of a general chiral auxiliary 2. Evaluation of camphor lactam imide auxiliaries for asymmetric aldol reactions

3. Toward the development of a general chiral auxiliary. 1. Preparation of a new class of camphor lactam imides and their application to the construction of quaternary centers via Diels-Alder cycloaddition.

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