Tetrahedron letters
Factors controlling the diastereoface selectivity in the complementary asymmetric alkylation of α-alkyl β-keto esters
K Tomioka, K Ando, Y Takemasa, K Koga
Index: Tomioka, Kiyoshi; Ando, Kaori; Takemasa, Yutaka; Koga, Kenji Tetrahedron Letters, 1984 , vol. 25, # 49 p. 5677 - 5680
Full Text: HTML
Citation Number: 25
Abstract
Abstract Complementary asymmetric alkylation reaction of the lithioenamine derived from 2- methoxycarbonylcyclohexanone and (S)-valine tert-butyl ester was examined by employing the various electron pair donating additives in a toluene solvent, in order to clarify the factors controlling the diastereoface selectivity.
Related Articles:
Asymmetric alkylation using chiral cyclic diols to prepare a quaternary carbon
[Kato, Keisuke; Suemune, Hiroshi; Sakai, Kiyoshi Tetrahedron, 1994 , vol. 50, # 11 p. 3315 - 3326]