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pubmed-article:18986143pubmed:abstractTextWe have developed low-valent titanium-mediated 1,3-transpositive cross-coupling reactions of acyclic and cyclic allylic alcohols for the stereoselective introduction of ethyl, 2-silylethyl, 2-phenethyl, and alkenyl groups. Cross-coupling of an allylic alcohol with a vinylsilane or styrene derivative is particularly noteworthy, as an efficient cross-selective coupling of two alkenes has been elusive. The stereochemistry of the cross-coupling alkylation is consistent with syn addition/beta-elimination.lld:pubmed
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pubmed-article:18986143pubmed:authorpubmed-author:ChaJin KunJKlld:pubmed
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pubmed-article:18986143pubmed:articleTitleLow-valent titanium-mediated stereoselective alkylation of allylic alcohols.lld:pubmed
pubmed-article:18986143pubmed:affiliationDepartment of Chemistry, Wayne State University, 5101 Cass Avenue, Detroit, Michigan 48202, USA.lld:pubmed
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