Diastereoselectivity in the synthesis of syn-cis-3a-hydroxypyrrolo[2,3-b] indoline Nα′-methyl-dipeptide methyl esters
Diastereoselectivity in the synthesis of syn-cis-3a-hydroxypyrrolo[2,3-b] indoline Nα′-methyl-dipeptide methyl esters
Described herein is a high yielding, diastereoselective synthesis of the syn-cis hydroxypyrroloindoline moiety by oxidation of the Nα-trityl- tryptophan-Nα-methyl-dipeptide methyl esters.
Diastereoselectivity, Hydroxypyrroloindole, Oxidation, Peptide natural products
3403-3406
May, Jonathan P.
b54a262b-9f32-4435-8866-3b9c495294f3
Patrick, Brian O.
44faf6ae-8ba6-4cb0-bcb7-0e7261948804
Perrin, David M.
12feb705-d3df-4f49-acf5-4283867ca47c
18 December 2006
May, Jonathan P.
b54a262b-9f32-4435-8866-3b9c495294f3
Patrick, Brian O.
44faf6ae-8ba6-4cb0-bcb7-0e7261948804
Perrin, David M.
12feb705-d3df-4f49-acf5-4283867ca47c
May, Jonathan P., Patrick, Brian O. and Perrin, David M.
(2006)
Diastereoselectivity in the synthesis of syn-cis-3a-hydroxypyrrolo[2,3-b] indoline Nα′-methyl-dipeptide methyl esters.
Synlett, (20), .
(doi:10.1055/s-2006-958427).
Abstract
Described herein is a high yielding, diastereoselective synthesis of the syn-cis hydroxypyrroloindoline moiety by oxidation of the Nα-trityl- tryptophan-Nα-methyl-dipeptide methyl esters.
This record has no associated files available for download.
More information
Published date: 18 December 2006
Keywords:
Diastereoselectivity, Hydroxypyrroloindole, Oxidation, Peptide natural products
Identifiers
Local EPrints ID: 455583
URI: http://eprints.soton.ac.uk/id/eprint/455583
ISSN: 0936-5214
PURE UUID: ec6d883f-25d1-4f00-a96f-2f4e416cc2fa
Catalogue record
Date deposited: 28 Mar 2022 16:38
Last modified: 17 Mar 2024 03:53
Export record
Altmetrics
Contributors
Author:
Brian O. Patrick
Author:
David M. Perrin
Download statistics
Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.
View more statistics
