Enantioselective Bromolactonization of Deactivated Olefinic Acids­: Studies Toward the Synthesis of Brominated Isochroman-1,4-diones

Enantioselective Bromolactonization of Deactivated Olefinic Acids­: Studies Toward the Synthesis of Brominated Isochroman-1,4-diones

Abstract Enantioselective bromolactonization using an amino-carbamate­ catalyst to generate brominated isochroman-1,4-diones is described. Excellent yields and moderate enantioselectivities were achieved.

Bibliographic Details
Main Authors: Danqing Li, Hailong He, Xiaodan Huang, Pei Yu, Xiaojian Jiang
Format: Article
Language:English
Published: Georg Thieme Verlag KG 2018-10-01
Series:SynOpen
Subjects:
isochroman-1,4-diones
bromolactonization
organocatalysis
enantioselectivity
deactivated olefins
Online Access:http://www.thieme-connect.de/DOI/DOI?10.1055/s-0037-1610401

Internet

http://www.thieme-connect.de/DOI/DOI?10.1055/s-0037-1610401

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