Jump to main content
Jump to site search
PLANNED MAINTENANCE Close the message box

Scheduled maintenance work on Wednesday 22nd May 2019 from 11:00 AM to 1:00 PM (GMT).

During this time our website performance may be temporarily affected. We apologise for any inconvenience this might cause and thank you for your patience.


Issue 47, 2013
Previous Article Next Article

Enantioselective total synthesis of (+)-brazilin, (−)-brazilein and (+)-brazilide A

Author affiliations

Abstract

An enantioselective strategy for the synthesis of (+)-brazilin, (−)-brazilein and (+)-brazilide A has been developed. A Lewis acid mediated lactonization established the novel fused bis-lactone core of brazilide A and finalized the first total synthesis of (+)-brazilide A.

Graphical abstract: Enantioselective total synthesis of (+)-brazilin, (−)-brazilein and (+)-brazilide A

Back to tab navigation

Supplementary files

Publication details

The article was received on 02 Apr 2013, accepted on 23 Apr 2013 and first published on 09 May 2013


Article type: Communication
DOI: 10.1039/C3CC42385A
Chem. Commun., 2013,49, 5405-5407

  •   Request permissions

    Enantioselective total synthesis of (+)-brazilin, (−)-brazilein and (+)-brazilide A

    X. Wang, H. Zhang, X. Yang, J. Zhao and C. Pan, Chem. Commun., 2013, 49, 5405
    DOI: 10.1039/C3CC42385A

Search articles by author

Spotlight

Advertisements