Oxidative rearrangement of 2-alkoxy-3,4-dihydro-2H-pyrans: stereocontrolled synthesis of 4,5-cis-disubstituted tetrahydrofuranones including whisky and cognac lactones and crobarbatic acid-Reference-Cited by-同舟云学术

Oxidative rearrangement of 2-alkoxy-3,4-dihydro-2H-pyrans: stereocontrolled synthesis of 4,5-cis-disubstituted tetrahydrofuranones including whisky and cognac lactones and crobarbatic acid

Published:2009-06 Issue:23 Volume:65 Page:4490-4504
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Armstrong Alan,Ashraff Cassim,Chung Hunsuk,Murtagh Lorraine

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference52 articles.

1. Strategy and Methodology Development for the Total Synthesis of Polyether Ionophore Antibiotics

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

3. Synthetic routes to 2,5-disubstituted tetrahydrofurans

4. Recent advances in the stereoselective synthesis of tetrahydrofurans

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