Synthesis and Assignment of the Absolute Configuration of Indenotryptoline Bisindole Alkaloid BE-54017-Reference-Cited by-同舟云学术

Synthesis and Assignment of the Absolute Configuration of Indenotryptoline Bisindole Alkaloid BE-54017

Published:2012-08-23 Issue:17 Volume:14 Page:4418-4421
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Kimura Tomoyuki¹,Kanagaki Shuhei¹,Matsui Yusuke¹,Imoto Masaya¹,Watanabe Takumi¹,Shibasaki Masakatsu¹

Affiliation:

1. Institute of Microbial Chemistry, Tokyo, 3-14-23 Kamiosaki, Shinagawa-ku, Tokyo 141-0021, Japan, and Faculty of Science and Technology, Department of Biosciences and Informatics, Keio University, Yokohama, 223-8522, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol3019314

Reference23 articles.

1. Divergent Pathways in the Biosynthesis of Bisindole Natural Products

2. Simple indole alkaloids and those with a nonrearranged monoterpenoid unit

3. Chemical biology of natural indolocarbazole products: 30 years since the discovery of staurosporine

4. Isolation and structure of rebeccamycin - a new antitumor antibiotic from nocardia aerocoligenes

5. Production and biological activity of rebeccamycin, a novel antitumor agent.

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