The first synthesis of a fully functionalized core structure of staurosporine: sequential indolyl glycosidation by endo and exo glycals

The first synthesis of a fully functionalized core structure of staurosporine: sequential indolyl glycosidation by endo and exo glycals

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Veröffentlicht in:Journal of the American Chemical Society 1993-05, Vol.115 (9), p.3782-3783
Hauptverfasser: Link, J. T, Gallant, Michel, Danishefsky, Samuel J, Huber, Susan
Format: Artikel
Sprache:eng
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Chemistry
Exact sciences and technology
Heterocyclic compounds
Heterocyclic compounds with n hetero atom and also o and/or s, se, te hetero atoms
Organic chemistry
Preparations and properties
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container_issue 9
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container_title Journal of the American Chemical Society
container_volume 115
creator Link, J. T
Gallant, Michel
Danishefsky, Samuel J
Huber, Susan
description
doi_str_mv 10.1021/ja00062a057
format Article
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source American Chemical Society Journals
subjects Chemistry
Exact sciences and technology
Heterocyclic compounds
Heterocyclic compounds with n hetero atom and also o and/or s, se, te hetero atoms
Organic chemistry
Preparations and properties
title The first synthesis of a fully functionalized core structure of staurosporine: sequential indolyl glycosidation by endo and exo glycals
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