Total synthesis of (−)-(6R,11R,14S)-colletallol via proline catalyzed α-aminoxylation and Yamaguchi macrolactonization-Reference-Cited by-同舟云学术

Total synthesis of (−)-(6R,11R,14S)-colletallol via proline catalyzed α-aminoxylation and Yamaguchi macrolactonization

Published:2016 Issue:68 Volume:6 Page:63607-63612
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Kauloorkar Shruti Vandana¹²³⁴,Kumar Pradeep¹²³⁴

Affiliation:

1. Division of Organic Chemistry

2. CSIR-NCL (National Chemical Laboratory)

3. Pune 411008

4. India

Abstract

A simple and efficient synthesis of 14-membered macrolide (−)-(6R,11R,14S)-colletallol was achieved in a highly diastereoselective manner using proline catalyzed alpha-aminoxylation and Yamaguchi protocol.

Funder

Council of Scientific and Industrial Research

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/RA/C6RA08484B

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