Bicyclic guanidinium-catalyzed enantioselective phase-transfer alkylation : direct access to pyrroloindolines and furoindolines

Highly enantioselective phase-transfer alkylation of 3-substituted-2-oxindoles with activated bromomethanes is disclosed with a broad substrate scope by using bicyclic guanidinium as a catalyst and a Lewis acid as the co-catalyst. The alkylation adducts are versatile intermediates to accomplish the...

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Bibliographic Details
Main Authors: Jiang, Zhiyong, Chen, Wenchao, Yang, Wenguo, Yan, Lin, Tan, Choon-Hong
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2013
Subjects:
Online Access:https://hdl.handle.net/10356/99510
http://hdl.handle.net/10220/17449
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Institution: Nanyang Technological University
Language: English
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Summary:Highly enantioselective phase-transfer alkylation of 3-substituted-2-oxindoles with activated bromomethanes is disclosed with a broad substrate scope by using bicyclic guanidinium as a catalyst and a Lewis acid as the co-catalyst. The alkylation adducts are versatile intermediates to accomplish the syntheses of pyrroloindolines and furoindolines.