Cyclization Strategies for the Synthesis of Macrocyclic Bisindolylmaleimides-Reference-Cited by-同舟云学术

Cyclization Strategies for the Synthesis of Macrocyclic Bisindolylmaleimides

Published:2001-03-01 Issue:6 Volume:66 Page:2024-2033
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Faul Margaret M.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/jo001605g

Reference12 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. Macrocyclic Bisindolylmaleimides: Synthesis by Inter- and Intramolecular Alkylation

3. A New, Efficient Method for the Synthesis of Bisindolylmaleimides

4. A new one step synthesis of maleimides by condensation of glyoxylate esters with acetamides

5. Synthesis of Rebeccamycin and 11-Dechlororebeccamycin

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