Diastereoselective α-iodination reaction of 4-alkenylamide having a β-chiral center

Autor:	Takeo Taguchi, Osamu Kitagawa, Tokushi Hanano, Masahiro Okada
Rok vydání:	1997
Předmět:	chemistry.chemical_compound Iodination reaction chemistry Stereochemistry Organic Chemistry Drug Discovery Acetal Ketene Center (algebra and category theory) Biochemistry
Zdroj:	Tetrahedron. 53:6825-6834
ISSN:	0040-4020
DOI:	10.1016/s0040-4020(97)00382-7
Popis:	α-Iodination reaction of 4-alkenylamide with a β-chiral center proceeds with high diastereoselectivity to give syn α-iodoalkenamide through the formation of cyclic ketene N , O -acetal and subsequent α-iodination from the opposite side of a β-substituent.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::950e74594dc6b9d4cf195bb17a3987aa https://doi.org/10.1016/s0040-4020(97)00382-7 Zobrazit plný text záznamu Full Text from ScienceDirect