Regioselective imide reduction: An issue in the total synthesis of staurosporine Journal Article

  


Authors: Link, J. T.; Danishefsky, S. J.
Article Title: Regioselective imide reduction: An issue in the total synthesis of staurosporine
Abstract: An imide was regioselectively reduced to either of its corresponding lactams. These lactams serve as potent glycosyl acceptors and can be converted into the aglycone of staurosporine. © 1994.
Keywords: drug synthesis; indole derivative; reaction analysis; stereochemistry; lactam derivative; staurosporine; article
Journal Title: Tetrahedron Letters
Volume: 35
Issue: 49
ISSN: 0040-4039
Publisher: Pergamon-Elsevier Science Ltd  
Date Published: 1994-12-05
Start Page: 9135
End Page: 9138
Language: English
DOI: 10.1016/0040-4039(94)88446-3
PROVIDER: scopus
DOI/URL:

https://www.scopus.com/inward/record.uri?eid=2-s2.0-0028148364&doi=10.1016%2f0040-4039%2894%2988446-3&partnerID=40&md5=210ff8d53534e79a1cdab9febee076db
Notes: Tetrahedron Lett. -- Cited By :30 -- Export Date: 14 January 2019 -- Article -- CODEN: TELEA -- Source: Scopus
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  1. Samuel J Danishefsky
    539 Danishefsky
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