Enolate-mediated 1,3-dipolar cycloaddition reactions of allyl ketones with nitrile oxides: direct access to 3,5-disubstituted isoxazolinesElectronic supplementary information (ESI) available. See DOI: 10.1039/c6ob02025a

TMG-promoted [3 + 2] organocatalytic 1,3-dipolar cycloaddition reactions of allyl ketones with in situ generated nitrile oxides have been developed. This strategy could generate 3,5-disubstituted isoxazolines in high yields and regioselectivities. TMG-catalyzed [3 + 2] organocatalytic 1,3-dipolar cy...

Full description

Saved in:
Bibliographic Details
Main Authors Li, Wenjun, Zhou, Xiao, Shi, Zhenyan, Liu, Yang, Liu, Zhantao, Gao, Hua
Format Journal Article
LanguageEnglish
Published 25.10.2016
Online AccessGet full text

Cover

More Information
Summary:TMG-promoted [3 + 2] organocatalytic 1,3-dipolar cycloaddition reactions of allyl ketones with in situ generated nitrile oxides have been developed. This strategy could generate 3,5-disubstituted isoxazolines in high yields and regioselectivities. TMG-catalyzed [3 + 2] organocatalytic 1,3-dipolar cycloaddition reactions of allyl ketones with in situ generated nitrile oxides have been developed. This strategy could generate 3,5-disubstituted isoxazolines in high yields and regioselectivities.
Bibliography:10.1039/c6ob02025a
Electronic supplementary information (ESI) available. See DOI
ISSN:1477-0520
1477-0539
DOI:10.1039/c6ob02025a