Synthetic and Mechanistic Studies of the Retro-Claisen Rearrangement. 3. A Route to Enantiomerically Pure Vinyl Cyclobutane Diesters via a Highly Diastereoselective Syn SN2‘ Reaction and Their Rearrangement to Enantiomerically Pure Dihydrooxacenes-Reference-Cited by-同舟云学术

Synthetic and Mechanistic Studies of the Retro-Claisen Rearrangement. 3. A Route to Enantiomerically Pure Vinyl Cyclobutane Diesters via a Highly Diastereoselective Syn SN2‘ Reaction and Their Rearrangement to Enantiomerically Pure Dihydrooxacenes

Published:1997-09-01 Issue:19 Volume:62 Page:6456-6457
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Boeckman Robert K.¹,Reeder Michael R.¹

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/jo9712254

Reference24 articles.

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2. Boeckman, R. K., Jr. New Methodology And Applications to the Synthesis ofAntibiotics and Other Bioactive Complex Molecules. In Antibiotic and AntiviralCompounds: Chemical Synthesis and Modification;Krohn, K. , Kirst, H. , Maas, H. , Eds.; VCH: Weinheim, 1993; pp 15−30.

3. Synthesis of Functionalized 2,5-Dihydrooxepines by [3,3]-Sigmatropic Rearrangement of Cyclopropane Derivatives

4. Total Synthesis of Brevetoxin B. 1. First Generation Strategies and New Approaches to Oxepane Systems

5. Trost, B. M. ; Verhoven, T. R. J. Org. Chem.1976,41, 3125.Trost, B. M. ; Weber, L. J. Am. Chem. Soc.1975,97, 1611.

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