Highly Regioselective Diels−Alder Reactions toward Oroidin Alkaloids: Use of a Tosylvinyl Moiety as a Nitrogen Masking Group with Adjustable Electronics-Reference-Cited by-同舟云学术

Highly Regioselective Diels−Alder Reactions toward Oroidin Alkaloids: Use of a Tosylvinyl Moiety as a Nitrogen Masking Group with Adjustable Electronics

Published:2005-04-01 Issue:9 Volume:7 Page:1679-1682
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Dransfield Paul J.¹,Wang Shaohui¹,Dilley Anja¹,Romo Daniel¹

Affiliation:

1. Department of Chemistry, Texas A&M University, P.O. Box 30012, College Station, Texas 77843-3012

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol0473602

Reference24 articles.

1. Ns strategies: a highly versatile synthetic method for amines

2. Enantioselective Strategy to the Spirocyclic Core of Palau'amine and Related Bisguanidine Marine Alkaloids

3. Highly Diastereoselective Desymmetrizations of Cyclo(Pro,Pro): An Enantioselective Strategy toward Phakellstatin and Phakellin

4. Enantioselective Total Synthesis of (+)-Dibromophakellstatin

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