Sequential application of stereoselective syn-oxidation methodologies to natural product synthesis: A potentially biomimetic approach to the C12–C21 bistetrahydrofuran region of monensin-Reference-Cited by-同舟云学术

Sequential application of stereoselective syn-oxidation methodologies to natural product synthesis: A potentially biomimetic approach to the C12–C21 bistetrahydrofuran region of monensin

Published:1997-12 Issue:48 Volume:53 Page:16435-16448
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

McDonald Frank E.,Schultz Colleen C.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference54 articles.

1. Polyether biosynthesis. 2. Origin of the oxygen atoms of monensin A

2. Unified stereochemical model of polyether antibiotic structure and biogenesis

3. Synthesis of the putative biosynthetic triene precursor of Monensin A

4. Asymmetric synthesis of premonensin, a potential intermediate in the biosynthesis of monensin

5. Synthesis of the proposed penultimate biosynthetic triene intermediate of monensin A

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