Catalytic and asymmetric [2, 3] sigmatropic rearrangement: Co (III)-salen catalyzed S-ylide formation from allyl aryl sulfides and their rearrangement
T Fukuda, R Irie, T Katsuki
Index: Fukuda, Tsutomu; Irie, Ryo; Katsuki, Tsutomu Tetrahedron, 1999 , vol. 55, # 3 p. 649 - 664
Full Text: HTML
Citation Number: 36
Abstract
Reaction of allyl aryl sulfides and α-diazoacetic acid esters in the presence of optically active Co (III)-salen complex (8-Br) provided 3-substituted 2-arylthio-4-pentenoic acid esters stereoselectively by way of enantioselective S-ylide formation and subsequent diastereoselective [2, 3] sigmatropic rearrangement. For example, the reaction of cinnamyl phenyl sulfide and (−)-menthyl α-diazoacetate provided (−)-menthyl (2R, 3S)-2-phenylthio ...
Related Articles:
[Cere, Vanda; Massaccesi, Franco; Pollicino, Salvatore; Ricci, Alfredo Synthetic Communications, 1996 , vol. 26, # 5 p. 899 - 907]
[Komine, Nobuyuki; Sako, Akari; Hirahara, Shin-Ya; Hirano, Masafumi; Komiya, Sanshiro Chemistry Letters, 2005 , vol. 34, # 2 p. 246 - 247]
[Bach, Thorsten; Koerber, Christina Journal of Organic Chemistry, 2000 , vol. 65, # 8 p. 2358 - 2367]
[Cere, Vanda; Massaccesi, Franco; Pollicino, Salvatore; Ricci, Alfredo Synthetic Communications, 1996 , vol. 26, # 5 p. 899 - 907]
[Cere, Vanda; Massaccesi, Franco; Pollicino, Salvatore; Ricci, Alfredo Synthetic Communications, 1996 , vol. 26, # 5 p. 899 - 907]