Spin-trapping Study of DNA Cleavage Induced by Enediyne C-1027 Chromophore
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Reference28 articles.
1. A new macromolecular antitumor antibiotic, C-1027. II. Isolation and physico-chemical properties.
2. A new macromolecular antitumor antibiotic, C-1027. III. Antitumor activity.
3. Structure of an aromatization product of C-1027 chromophore
4. Reaction of C60 with diacyl peroxides containing perfluoroalkyl groups. The first example of electron transfer reaction via C60+· in solution
5. Synthesis and absolute stereochemistry of the aminosugar moiety of antibiotic C-1027 chromophore
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1. Total synthesis and related studies of large, strained, and bioactive natural products;Proceedings of the Japan Academy, Series B;2016
2. A Synthetic and Mechanistic Investigation of the Chromium Tricarbonyl-Mediated Masamune–Bergman Cyclization. Direct Observation of a Ground-State Tripletp-Benzyne Biradical;Organometallics;2012-07-13
3. Spin-Trapping of the p-Benzyne Intermediates from Ten-Membered Enediyne Calicheamicin γ1I;Organic Letters;2006-10-31
4. Antitumor Enediyne Chromoprotein C-1027: Mechanistic Investigation of the Chromophore-Mediated Self-Decomposition Pathway;Journal of the American Chemical Society;2006-05-24
5. Exploring the Chemistry and Biology of Antitumor Enediyne Chromoprotein C-1027;Bulletin of the Chemical Society of Japan;2006-04
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