Catalyst-Controlled Asymmetric Synthesis of Fostriecin and 8-epi-Fostriecin-Reference-Cited by-同舟云学术

Catalyst-Controlled Asymmetric Synthesis of Fostriecin and 8-epi-Fostriecin

Published:2005-11-10 Issue:48 Volume:127 Page:17111-17117
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Maki Keisuke¹,Motoki Rie¹,Fujii Kunihiko¹,Kanai Motomu¹,Kobayashi Takayasu¹,Tamura Shinri¹,Shibasaki Masakatsu¹

Affiliation:

1. Contribution from the Graduate School of Pharmaceutical Sciences, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo 113-0033, Japan, and Department of Biochemistry, Institute of Development, Aging and Cancer, Tohoku University, Seiryo-machi, Aobaku, Sendai, 980-8570, Japan

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja0562043

Reference49 articles.

1. Novel antitumor agents CI-920,PD113,270 and PD113,271. I. Taxonomy, fermentation and biological properties.

2. Novel antitumor agents CI-920,PD113,270 and PD113,271. II. Isolation and characterization.

3. Fostriecin: Chemistry and Biology

4. Chromosome condensation induced by fostriecin does not require p34cdc2 kinase activity and histone H1 hyperphosphorylation, but is associated with enhanced histone H2A and H3 phosphorylation.

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