An efficient synthesis of substituted 3(4)-nitropyrroles from nitroalkenes and tosylmethyl isocyanides

Autor:	F. R. Leusink, Ronald ten Have, A. M. Van Leusen
Přispěvatelé:	Molecular Inorganic Chemistry
Jazyk:	angličtina
Rok vydání:	1996
Předmět:	chemistry.chemical_compound RING PYRROLES chemistry CHEMISTRY Organic Chemistry TosMIC Organic chemistry IMIDAZOLES Tosylmethyl isocyanide Ring (chemistry) Catalysis SULFONYLMETHYL ISOCYANIDES
Zdroj:	Synthesis-Stuttgart, 871-876. GEORG THIEME VERLAG KG ISSUE=7;STARTPAGE=871;ENDPAGE=876;ISSN=0039-7881;TITLE=Synthesis-Stuttgart
ISSN:	0039-7881
Popis:	A series of 3(4)-nitropyrroles with alkenyl substituents in the 2- and 3-positions (or 3-position only) is synthesized efficiently in one operation by a base-induced addition of tosylmethyl isocyanide (TosMIC), or unsaturated homologs of TosMIC, to nitroalkenes.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a643a1f83cdcf7eb894e21905e9c517 https://research.rug.nl/en/publications/3e48a8b0-63ba-4018-9a4b-d73d8aa236a5 Zobrazit plný text záznamu