Divergent Synthesis of α,γ-Disubstituted γ-Butyrolactones through Diastereoselective Bromolactonization with Alkali Metal Bromide: Asymmetric Total Synthesis of (+)-Dubiusamine C-Reference-Cited by-同舟云学术

Divergent Synthesis of α,γ-Disubstituted γ-Butyrolactones through Diastereoselective Bromolactonization with Alkali Metal Bromide: Asymmetric Total Synthesis of (+)-Dubiusamine C

Published:2015-08-27 Issue:18 Volume:80 Page:9132-9140
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Moriyama Katsuhiko¹,Sugiue Toru¹,Nishinohara Chihiro¹,Togo Hideo¹

Affiliation:

1. Department of Chemistry, Graduate School of Science, Chiba University, 1-33 Yayoi-cho, Inage-ku, Chiba 263-8522, Japan

Funder

Ministry of Education, Culture, Sports, Science, and Technology

Naito Foundation

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.5b01497

Reference65 articles.

1. Synthesis and Biological Activity of ?-Methylene-?-butyrolactones

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3. Paraconic Acids—The Natural Products from Lichen Symbiont

4. Assignment of Absolute Stereochemistry and Total Synthesis of (−)-Spongidepsin

5. Synthetic Studies on (+)-Ophiobolin A: Asymmetric Synthesis of the Spirocyclic CD-Ring Moiety

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