前往化源商城

Tetrahedron

Aryl-and alkynyltri-isopropoxytitanium reagents in regioselective carbon-carbon bond formation in azines

LL Gundersen, F Rise, K Undheim

文献索引:Gundersen, Lise-Lotte; Rise, Frode; Undheim, Kjell Tetrahedron, 1992 , vol. 48, # 27 p. 5647 - 5656

全文:HTML全文

被引用次数: 24

摘要

Regioselective arylation in the 4-position in pyridines results from 1: 1-adduct formation between an aryltriisopropoxytitanium reagent and N-isobutyloxycarbonyl-or an N- silyloxymethyl-3-cyanopyridinium salt after successive DDQ dehydrogenation and cleavage of the 1-substituent. Complete regioselectivity for new C C bond formation in the 4-position results in the adduct formation between aryl-and phenylethynyltri-isopropoxytitanium ...