Journal of Organic Chemistry p. 4370 - 4382 (1991)
Update date:2022-08-03
Topics:
Ibuka, Toshiro
Habashita, Hiromu
Otaka, Akira
Fujii, Nobutaka
Oguchi, Yusaku
Uyehara, Tadao et al.
A stereoselective synthesis of protected (E)-alkene dipeptide isosteres by the reaction of the mesylates of homochiral δ-aminated γ-hydroxy (E)-α,β-enoates with either RCu(CN)Li-BF3 or RCu(CN)MgX.BF3 reagent is described.The degree of diastereoselectivity
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Doi:10.1055/s-1999-2935
(1999)Doi:10.1039/c1ob06112g
(2011)Doi:10.1016/j.poly.2011.08.011
(2011)Doi:10.1016/S0040-4039(00)79649-3
(1991)Doi:10.1016/S0022-1139(00)80196-7
(1991)Doi:10.1016/S0022-1139(00)83619-2
(1991)
