Catalytic asymmetric 6pi electrocyclization: enantioselective synthesis of functionalized indolines.
(figure represented) How to close a ring: An approach to catalytic asymmetric 6π electrocyclization leads to a highly enantioselective process that was used in the synthesis of chiral indolines (see scheme). Treatment of N-aryl imines under phase transfer conditions in the presence of N-benzyl cinch...
Main Authors: | Maciver, E, Thompson, S, Smith, M |
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Formato: | Journal article |
Idioma: | English |
Publicado em: |
2009
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