Method for synthesis of 12H-pyrido[1,2-a:3,4-b']diindoles. Total synthesis of homofascaplysin C

Autor:	Sergey V. Dubovitskii
Rok vydání:	1996
Předmět:	Reaction sequence Stereochemistry Homofascaplysin C Chemistry Organic Chemistry Drug Discovery Total synthesis Dehydrogenation Formyl group Biochemistry
Zdroj:	Tetrahedron Letters. 37:5207-5208
ISSN:	0040-4039
Popis:	An efficient synthesis of a 12H-pyrido[1,2-a:3,4-b']diindole system is proposed. 3-Methylindole has been converted into homofascaplysin C by a four reaction sequence in which the last step is dehydrogenation and oxidation of the methyl- to formyl group at the same time.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::73b6d2d2063efc04ac3834a158724e3f https://doi.org/10.1016/0040-4039(96)01052-0 Zobrazit plný text záznamu Full Text from ScienceDirect