Regioselective S-allylation of thiols with cyclic Baylis–Hillman acetates
I Erray, J Oble, G Poli, F Rezgui
Index: Erray, Imen; Oble, Julie; Poli, Giovanni; Rezgui, Farhat Journal of Sulfur Chemistry, 2014 , vol. 35, # 2 p. 128 - 136
Full Text: HTML
Citation Number: 4
Abstract
Therefore, a clean and economical S-allylation is still a very attractive goal for the construction of carbon–sulfur bonds, especially in functionalized allylic compounds such as Baylis–Hillman (BH) adducts. As it so happens, reactions of acyclic BH acetates with thiols,[2222. Kamimura A, Morita R, Matsuura K, Mitsudera H, Shirai M. A convenient stereoselective synthesis of β-lactams from β-hydroxy-α-thioalkylesters prepared from Michael/aldol tandem reaction or ...
Related Articles:
[Tamura, Rui; Katayama, Hitoshi; Watabe, Ken-Ichiro; Suzuki, Hitomi Tetrahedron, 1990 , vol. 46, # 21 p. 7557 - 7568]
[Tamura, Rui; Katayama, Hitoshi; Watabe, Ken-Ichiro; Suzuki, Hitomi Tetrahedron, 1990 , vol. 46, # 21 p. 7557 - 7568]
[Tamura, Rui; Katayama, Hitoshi; Watabe, Ken-Ichiro; Suzuki, Hitomi Tetrahedron, 1990 , vol. 46, # 21 p. 7557 - 7568]
[Tamura, Rui; Tamai, Shinobu; Suzuki, Hitomi Tetrahedron Letters, 1989 , vol. 30, # 18 p. 2413 - 2416]
[Tamura, Rui; Tamai, Shinobu; Suzuki, Hitomi Tetrahedron Letters, 1989 , vol. 30, # 18 p. 2413 - 2416]