Jump to main content
Jump to site search
Access to RSC content Close the message box

Continue to access RSC content when you are not at your institution. Follow our step-by-step guide.


Issue 3, 2018
Previous Article Next Article

Rapid, enantioselective synthesis of the C1–C13 fragment of biselyngbyolide B

Author affiliations

Abstract

A rapid synthesis of the C1–C13 fragment of biselynbyolide A and B is reported. The judicious use of catalytic transformations for C–C bond formation and stereocenter generation greatly minimizes the use of protecting groups and oxidation state changes, as compared to previously reported routes to similar fragments.

Graphical abstract: Rapid, enantioselective synthesis of the C1–C13 fragment of biselyngbyolide B

Back to tab navigation

Supplementary files

Article information


Submitted
16 Oct 2017
Accepted
28 Nov 2017
First published
28 Nov 2017

Chem. Commun., 2018,54, 241-243
Article type
Communication

Rapid, enantioselective synthesis of the C1–C13 fragment of biselyngbyolide B

R. G. Thorat and A. M. Harned, Chem. Commun., 2018, 54, 241
DOI: 10.1039/C7CC08004B

Social activity

Search articles by author

Spotlight

Advertisements