An enantioselective synthesis of (+)-(S)-[n]-gingerols via the l-proline-catalyzed aldol reaction
An enantioselective approach to (+)-(S)-[n]-gingerols (1a-c) has been developed. The requisite stereogenic centers of target molecules are facilely constructed by the proline-catalyzed cross-aldol reaction from readily available achiral starting materials
Ma, Shichao,Zhang, Shilei,Duan, Wenhu,Wang, Wei
supporting information; experimental part
p. 3909 - 3911
(2010/03/25)
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