Stereospecific synthesis of EET metabolites via Suzuki–Miyaura coupling

Autor:	Y. Krishna Reddy, Jorge H. Capdevila, Gang Zou, P. Srinagesh Kumar, John R. Falck
Rok vydání:	2001
Předmět:	Coupling (electronics) Stereospecificity Stereochemistry Chemistry Organic Chemistry Drug Discovery lipids (amino acids peptides and proteins) Biochemistry
Zdroj:	Tetrahedron Letters. 42:7211-7212
ISSN:	0040-4039
DOI:	10.1016/s0040-4039(01)01535-0
Popis:	Bioactive, chain-shortened EET metabolites, viz. 8,9-epoxytetradec-5(Z)-enoic acid and 9,10-epoxyoctadec-6(Z),12(Z)-dienoic acid, were prepared via Suzuki–Miyaura cross-couplings of n-alkylboronic acids with chiral vinyl iodides.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::a624bdd34f9a98a8d1c386674e9fe32f https://doi.org/10.1016/s0040-4039(01)01535-0 Zobrazit plný text záznamu Full Text from ScienceDirect