Catalytic asymmetric 6pi electrocyclization: enantioselective synthesis of functionalized indolines.

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...

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Chi tiết về thư mục
Những tác giả chính:	Maciver, E, Thompson, S, Smith, M
Định dạng:	Journal article
Ngôn ngữ:	English
Được phát hành:	2009

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