The effect of remote oxygens on the ring-opening reactions of oxabicyclic compounds with organolithium reagents. Synthesis of the C21–C27 segment of rifamycin S-Reference-Cited by-同舟云学术

The effect of remote oxygens on the ring-opening reactions of oxabicyclic compounds with organolithium reagents. Synthesis of the C21–C27 segment of rifamycin S

Published:1992-05 Issue:19 Volume:33 Page:2617-2620
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Lautens Mark,Belter Randolph K.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference26 articles.

1. Opening of oxabicyclo[3.2.1]octenes with organolithium reagents. A route to cyclic and acyclic compounds with high stereocontrol

2. Regio- and stereospecific synthesis of substituted cyclohexenediols from 7-oxabicyclo[2.2.1]hept-5-en-2-ols and organolithium reagents

3. Ring-opening reactions of an oxabicyclic compound with cuprates

4. Total synthesis of rifamycins. 1. Stereocontrolled synthesis of the aliphatic building block

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