Transition-metal binding site of bleomycin. A synthetic analogue equivalent to bleomycin in activating molecular oxygen
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference8 articles.
1. Kittaka, A.; Sugano, Y.; Otsuka, M.; Ohno, M.; Sugiura, Y.; Umezawa, H. Preceding paper of this issue.
2. Synthetic studies on an antitumor antibiotic, bleomycin. XII. Preparation of an L-2,3-diaminopropionic acid derivative as a synthetic intermediate.
3. New Methods in Peptide Synthesis. I. Tritylsulfenyl and o-Nitrophenylsulfenyl Groups as N-Protecting Groups
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