Stereoselective Synthesis of 2,6-cis-Tetrahydropyrans through a Tandem Allylic Oxidation/Oxa-Michael Reaction Promoted by thegem-Disubstituent Effect: Synthesis of (+)-Neopeltolide Macrolactone-Reference-Cited by-同舟云学术

Stereoselective Synthesis of 2,6-cis-Tetrahydropyrans through a Tandem Allylic Oxidation/Oxa-Michael Reaction Promoted by thegem-Disubstituent Effect: Synthesis of (+)-Neopeltolide Macrolactone

Published:2009-09-28 Issue:41 Volume:48 Page:7577-7581
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Kim Hyoungsu,Park Yongho,Hong Jiyong

Publisher

Wiley

Subject

General Chemistry,Catalysis

Reference62 articles.

1. For reviews on THP synthesis, see:

2. Synthetic routes to tetrahydrofuran, tetrahydropyran, and spiroketal units of polyether antibiotics and a survey of spiroketals of other natural products

3. Strategies for the Formation of Tetrahydropyran Rings in the Synthesis of Natural Products

4. Synthesis of six-membered oxygenated heterocycles through carbon–oxygen bond-forming reactions

5. The oxa-Michael reaction: from recent developments to applications in natural product synthesis

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