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Stereoselective synthesis of brevianamide E

Stereoselective synthesis of brevianamide E
Stereoselective synthesis of brevianamide E

The hydroxypyrroloindolenine (Hpi) motif forms the fundamental core of the pentacyclic natural product, brevianamide E, the concise stereoselective synthesis of which, via oxidative cyclization, is described.

1523-7060
90-93
Zhao, Liang
8a8924b8-aa93-4e73-91ea-5e9ae1db8afc
May, Jonathan P.
b54a262b-9f32-4435-8866-3b9c495294f3
Huang, Jack
419b9ddc-1e63-4f7e-a509-3376999e1e85
Perrin, David M.
12feb705-d3df-4f49-acf5-4283867ca47c
Zhao, Liang
8a8924b8-aa93-4e73-91ea-5e9ae1db8afc
May, Jonathan P.
b54a262b-9f32-4435-8866-3b9c495294f3
Huang, Jack
419b9ddc-1e63-4f7e-a509-3376999e1e85
Perrin, David M.
12feb705-d3df-4f49-acf5-4283867ca47c

Zhao, Liang, May, Jonathan P., Huang, Jack and Perrin, David M. (2012) Stereoselective synthesis of brevianamide E. Organic Letters, 14 (1), 90-93. (doi:10.1021/ol202880y).

Record type: Article

Abstract

The hydroxypyrroloindolenine (Hpi) motif forms the fundamental core of the pentacyclic natural product, brevianamide E, the concise stereoselective synthesis of which, via oxidative cyclization, is described.

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More information

Published date: 6 January 2012
Additional Information: Copyright: Copyright 2012 Elsevier B.V., All rights reserved.

Identifiers

Local EPrints ID: 452477
URI: http://eprints.soton.ac.uk/id/eprint/452477
ISSN: 1523-7060
PURE UUID: 106e4089-31d6-4c45-9d6b-b131d0227a81
ORCID for Jonathan P. May: ORCID iD orcid.org/0000-0003-1651-130X

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Date deposited: 11 Dec 2021 11:15
Last modified: 17 Mar 2024 03:53

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Contributors

Author: Liang Zhao
Author: Jonathan P. May ORCID iD
Author: Jack Huang
Author: David M. Perrin

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