Transformation of Renieramycin M into Renieramycins T and S by Intramolecular Photoredox Reaction of 7-Methoxy-6-methyl-1,2,3,4-tetrahydroisoquinoline-5,8-dione Derivatives-Reference-Cited by-同舟云学术

Transformation of Renieramycin M into Renieramycins T and S by Intramolecular Photoredox Reaction of 7-Methoxy-6-methyl-1,2,3,4-tetrahydroisoquinoline-5,8-dione Derivatives

Published:2023-01-11 Issue:1 Volume:86 Page:222-231
ISSN:0163-3864
Container-title:Journal of Natural Products
language:en
Short-container-title:J. Nat. Prod.

Author:

Yokoya Masashi¹^ORCID,Yamazaki-Nakai Miku¹,Nakai Keiyo¹,Sirimangkalakitti Natchanun¹,Chamni Supakarn²^ORCID,Suwanborirux Khanit²^ORCID,Saito Naoki¹^ORCID

Affiliation:

1. Graduate School of Pharmaceutical Sciences, Meiji Pharmaceutical University, 2-522-1 Noshio, Kiyose, Tokyo 204-8588, Japan

2. Department of Pharmacognosy and Pharmaceutical Botany, Faculty of Pharmaceutical Sciences, Chulalongkorn University, Bangkok 10330, Thailand

Funder

Ministry of Education, Culture, Sports, Science and Technology

Japan Society for the Promotion of Science

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Complementary and alternative medicine,Drug Discovery,Pharmaceutical Science,Pharmacology,Molecular Medicine,Analytical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.jnatprod.2c00974

Reference41 articles.

1. Chemical Research on Antitumor Isoquinoline Marine Natural Products and Related Compounds

2. aKubo, A.; Saito, N. Studies in Natural Products Chemistry, Vol. 10; Atta-ur-Rahman, Ed. Elsevier: Amsterdam, 1992; pp 77–145.

3. Chemistry and Biology of the Tetrahydroisoquinoline Antitumor Antibiotics

4. Studies directed towards total synthesis of saframycin: I. A synthesis of hexahydro-1,5-imino-3-benzazocin-7,10-dione.

5. Synthesis of saframycins. II. Preparations and reactions of N-methyl-2,5-piperazinediones.

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