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Synthetic studies on mitomycins part II. Synthesis of aziridino-pyrrolo(1,2-a) indoles.

✍ Scribed by Tadashi Hirata; Yasuhiro Yamada; Masanao Matsui


Publisher
Elsevier Science
Year
1969
Tongue
French
Weight
176 KB
Volume
10
Category
Article
ISSN
0040-4039

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✦ Synopsis


As&i-ma&i lachida-shi lbkyu Japan,


πŸ“œ SIMILAR VOLUMES


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## Mitomycin antibiotics (I) have a novel ring system that is aziridinopyrrolo II 1,2-a indoloquinone(1). In synthetic studies on mitomycin analogs Lederle group synthesised 7-benzyloxy-9H-pyrrolo 1,2-a indole(2) and substituted 2,3r.

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## Abstract A new method for the synthesis of pyrrolo[1,2‐__a__]indoles, starting from enamines via 1,5‐dipolar cyclization is described. The method is considered to be useful for the synthesis of mitomycin type of compounds.

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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a β€œFull Text” option. The original article is trackable v