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.
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
6 January 2012
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), .
(doi:10.1021/ol202880y).
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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Published date: 6 January 2012
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Copyright 2012 Elsevier B.V., All rights reserved.
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Local EPrints ID: 452477
URI: http://eprints.soton.ac.uk/id/eprint/452477
ISSN: 1523-7060
PURE UUID: 106e4089-31d6-4c45-9d6b-b131d0227a81
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Date deposited: 11 Dec 2021 11:15
Last modified: 17 Mar 2024 03:53
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Author:
Liang Zhao
Author:
Jack Huang
Author:
David M. Perrin
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