贝克曼重排
化学
氨基酸
对映选择合成
有机化学
立体化学
肟
催化作用
生物化学
作者
Rogelio P. Frutos,Denice M. Spero
标识
DOI:10.1016/s0040-4039(98)00309-8
摘要
The synthesis of chiral, nonracemic, fully protected α,α-disubstituted α-amino acids via the Beckmann rearrangement of tosylated oximes 1 is described. The desired amino acids were obtained in good yields with excellent enantioselectivities in relatively few steps.
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