Asymmetric Total Synthesis of (+)-Bermudenynol, a C15LaurenciaMetabolite with a Vinyl Chloride Containing Oxocene Skeleton, through Intramolecular Amide Enolate Alkylation-Reference-Cited by-同舟云学术

Asymmetric Total Synthesis of (+)-Bermudenynol, a C15LaurenciaMetabolite with a Vinyl Chloride Containing Oxocene Skeleton, through Intramolecular Amide Enolate Alkylation

Published:2013-11-13 Issue:1 Volume:53 Page:272-276
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Kim Gyudong,Sohn Te-ik,Kim Deukjoon,Paton Robert S.

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/anie.201308077/fullpdf

Reference71 articles.

1. A Unifying Stereochemical Analysis for the Formation of Halogenated C15-Acetogenin Medium-Ring Ethers From Laurencia Species via Intramolecular Bromonium Ion Assisted Epoxide Ring-Opening and Experimental Corroboration with a Model Epoxide

2. Secondary metabolites from the red alga Laurenciaintricata: halogenated enynes

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