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:126 Page:276-280
ISSN:0044-8249
Container-title:Angewandte Chemie
language:de
Short-container-title:Angew. Chem.

Author:

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

Publisher

Wiley

Subject

General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ange.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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1. Total Synthesis of Two Possible Diastereomers of Natural 6-Chlorotetrahydrofuran Acetogenin and Its Stereostructural Elucidation;Chemistry - A European Journal;2017-11-22

2. Oxidative Alkoxycarbonylation of Alkynes by Means of Aryl α-Diimine Palladium(II) Complexes as Catalysts;Advanced Synthesis & Catalysis;2016-08-31

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4. Proof-of-principle direct double cyclisation of a linear C15-precursor to a dibrominated bicyclic medium-ring ether relevant toLaurenciaspecies;Chem. Commun.;2014