Title of article
Facile synthesis of γ-alkenylbutenolides from Baylis–Hillman adducts: consecutive in-mediated Barbier allylation, PCC oxidation, isomerization, and Zn-mediated Barbier allylation
Author/Authors
Lim، نويسنده , , Jin Woo and Kim، نويسنده , , Ko Hoon and Park، نويسنده , , Bo Ram and Kim، نويسنده , , Jae Nyoung، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2011
Pages
5
From page
6545
To page
6549
Abstract
Alkenylbutenolides were synthesized regioselectively in good to moderate yields from Baylis–Hillman adducts via a consecutive indium-mediated Barbier type reaction between Baylis–Hillman bromide and aldehyde, PCC oxidation of the homoallylic alcohol, double bond isomerization, and zinc-mediated Barbier type alkenylation protocol.
Keywords
Zinc , Baylis–Hillman adducts , Barbier reaction , ?-Alkenylbutenolides , Indium
Journal title
Tetrahedron Letters
Serial Year
2011
Journal title
Tetrahedron Letters
Record number
1879650
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