Zinc-mediated domino elimination–alkylation of methyl 5-iodopentofuranosides: an easy route to unsaturated carbohydrates for transition metal-catalyzed carbocyclizations
Zinc-mediated domino elimination–alkylation of methyl 5-iodopentofuranosides: an easy route to unsaturated carbohydrates for transition metal-catalyzed carbocyclizations
Carbohydrate Carbocyclization by a Novel Zinc-Mediated Domino Reaction and Ring-Closing Olefin Metathesis
作者:Lene Hyldtoft、Robert Madsen
DOI:10.1021/ja001415n
日期:2000.9.1
is described using two consecutive organometallic transformations: a novel zinc-mediated domino reaction to give functionalized dienes followed by ring-closing olefin metathesis. In the first reaction, methyl ω-deoxy-ω-iodo glycosides undergo reductive elimination with zinc to produce a terminal double bond. This also liberates the aldehyde which is immediately alkylated in situ by various organozinc
Zinc-mediated domino elimination–alkylation of methyl 5-iodopentofuranosides: an easy route to unsaturated carbohydrates for transition metal-catalyzed carbocyclizations
5-Iodopentofuranosides are converted with zinc and allyl/propargyl bromide into dienes/enynes which are further used in carbohydrate annulation reactions.