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Asymmetric Radical and Anionic Cyclizations of Axially Chiral Carbamates.

  作者 Guthrie, David B.;Curran, Dennis P.;  
  选自 期刊  Organic Letters;  卷期  2009年11-1;  页码  249-251  
  关联知识点  
 

[摘要]whose racemization barriers exceed 30 kcal/mol. The resolved axially chiral carbamates undergo radical and anionic cyclizations with high levels of chirality transfer from the N-Ar axis to the new stereocenter in the substituted dihydroindole products. The carbamate groups of the products are readily removed.

 
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