A New, Efficient Method for the Synthesis of Bisindolylmaleimides-Reference-Cited by-同舟云学术

A New, Efficient Method for the Synthesis of Bisindolylmaleimides

Published:1998-07-24 Issue:17 Volume:63 Page:6053-6058
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Faul Margaret M.¹,Winneroski Leonard L.¹,Krumrich Christine A.¹

Affiliation:

1. Lilly Research Laboratories, A Division of Eli Lilly and Company, Chemical Process Research and Development Division, Indianapolis, Indiana 46285-4813

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo980513c

Reference25 articles.

1. (S)-13-[(Dimethylamino)methyl]-10,11,14,15-tetrahydro-4,9:16,21-dimetheno- 1H,13H-dibenzo[e,k]pyrrolo[3,4-h][1,4,13]oxadiazacyclohexadecene-1,3(2H)-dione (LY333531) and Related Analogues: Isozyme Selective Inhibitors of Protein Kinase Cβ

2. Amelioration of Vascular Dysfunctions in Diabetic Rats by an Oral PKC β Inhibitor

3. Macrocyclic Bisindolylmaleimides: Synthesis by Inter- and Intramolecular Alkylation

4. First Total Synthesis of Staurosporine and ent-Staurosporine

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

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