Total Synthesis of Ecteinascidin 743-Reference-Cited by-同舟云学术

Total Synthesis of Ecteinascidin 743

Published:2002-05-17 Issue:23 Volume:124 Page:6552-6554
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Endo Atsushi¹,Yanagisawa Arata¹,Abe Masanao¹,Tohma Shigemitsu¹,Kan Toshiyuki¹,Fukuyama Tohru¹

Affiliation:

1. Graduate School of Pharmaceutical Sciences, The University of Tokyo, CREST, The Japan Science and Technology Cooperation (JST), 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja026216d

Reference21 articles.

1. Ecteinascidins 729, 743, 745, 759A, 759B, and 770: potent antitumor agents from the Caribbean tunicate Ecteinascidia turbinata

2. Additional antitumor ecteinascidins from a Caribbean tunicate: crystal structures and activities in vivo.

3. Antiproliferative activity of ecteinascidin 743 is dependent upon transcription-coupled nucleotide-excision repair

4. Enantioselective Total Synthesis of Ecteinascidin 743

Cited by 307 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Advances of Ugi reaction in natural product synthesis;Green Synthesis and Catalysis;2024-08

2. Transition-Metal-Catalyzed Transformations for the Synthesis of Marine Drugs;Marine Drugs;2024-05-29

3. An aminobenzannulation reaction of a propargylic ester and isocyanides to access multi-functionalized aryl amine derivatives;Organic Chemistry Frontiers;2024

4. Recent developments in the total synthesis of natural products using the Ugi multicomponent reactions as the key strategy;Organic & Biomolecular Chemistry;2024

5. Recent advances in post Ugi-4CR dearomatizations for constructing spiro heterocycles;Organic Chemistry Frontiers;2024