Specific 1,2-Hydride Shift in the Boron Trifluoride Catalyzed Reactions of Aromatic Aldehydes with Diazoacetonitrile: Simple Synthesis of β-Ketonitriles-Reference-Cited by-同舟云学术

Specific 1,2-Hydride Shift in the Boron Trifluoride Catalyzed Reactions of Aromatic Aldehydes with Diazoacetonitrile: Simple Synthesis of β-Ketonitriles

Published:2014-09-08 Issue:29 Volume:2014 Page:6380-6384
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Yang Zhanhui,Son Kwon-Il,Li Siqi,Zhou Bingnan,Xu Jiaxi

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference80 articles.

1. A Metal-Free Tandem C–C/C–O Bond Formation Approach to Diversely Functionalized Tetrasubstituted Furans

2. Enantioselective Reduction of α-Cyano and α-Nitro Substituted Acetophenones Promoted by a Bifunctional Mesoporous Silica

3. Efficient Enantioselective Synthesis of Dihydropyrans Using a Chiral N,N′-Dioxide as Organocatalyst

4. Rhodium-Catalyzed Cascade Oxidative Annulation Leading to Substituted Naphtho[1,8-bc]pyrans by Sequential Cleavage of C(sp2)–H/C(sp3)–H and C(sp2)–H/O–H Bonds

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