An Intramolecular Diels−Alder Strategy for the Asbestinins: Enantioselective Total Syntheses of 11-Acetoxy-4-deoxyasbestinin D and Asbestinin-12-Reference-Cited by-同舟云学术

An Intramolecular Diels−Alder Strategy for the Asbestinins: Enantioselective Total Syntheses of 11-Acetoxy-4-deoxyasbestinin D and Asbestinin-12

Published:2007-10-05 Issue:5 Volume:73 Page:1649-1660
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Crimmins Michael T.¹,Ellis J. Michael¹

Affiliation:

1. Department of Chemistry, Venable and Kenan Laboratories of Chemistry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599-3290

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0712695

Reference57 articles.

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4. Synthesis of the Alleged Structure of Sclerophytin A. The Setting of Two Oxygen Bridges within the Fused Cyclodecanol B Ring Is Not Nature's Way

5. Total Synthesis of the Supposed Structure of (−)-Sclerophytin A and an Improved Route to (−)-7-Deacetoxyalcyonin Acetate

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