Glycal approach to the synthesis of macrolide (−)-A26771B-Reference-Cited by-同舟云学术

Glycal approach to the synthesis of macrolide (−)-A26771B

Published:2015 Issue:37 Volume:5 Page:29114-29120
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Saidhareddy Puli¹²³⁴,Shaw Arun K.¹²³⁴

Affiliation:

1. Medicinal and Process Chemistry Division

2. CSIR-Central Drug Research Institute (CDRI)

3. Lucknow-226031

4. India

Abstract

A convergent synthesis of macrolide natural product (−)-A26771B starting from d-glucal is reported. Key features of this synthesis involve Ferrier rearrangement, cross metathesis of chiral fragments 3 and 4 and Yamaguchi macrolactonization.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/RA/C4RA17084A

Reference42 articles.

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