Pyrroloindoles. 12. Synthesis of 1H, 10H-benzo[e]pyrrolo[3,2-g]indole

Autor:	Sh. A. Samsonia, N. A. Kuprashvili, A. M. Kolesnikov, M. V. Trapaidze, N. N. Suvorov
Rok vydání:	1985
Předmět:	Indole test Hydrolysis chemistry.chemical_compound chemistry Decarboxylation Polyphosphate Organic Chemistry Organic chemistry Ethyl pyruvate
Zdroj:	Chemistry of Heterocyclic Compounds. 21:1016-1018
ISSN:	1573-8353 0009-3122
Popis:	Cyclization of ethyl pyruvate 2,3-naphthylenehydrazone in polyphosphate ester gives 2,9-diethoxycarbonyl-1H,10H-benzo[e]pyrrolo[3,2-g]indole, which on hydrolysis and decarboxylation of the resulting acid affords the unsubtituted 1H,10H-benzo[e] pyrrolo[3,2-g]indole.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::7878e0721a988c33622647cec966af0f https://doi.org/10.1007/bf00515026 Zobrazit plný text záznamu Full text from SpringerLink