Aminocarbonylation of Aryl Halides to Produce Primary Amides by Using NH4 HCO3 Dually as Ammonia Surrogate and Base-Reference-Cited by-同舟云学术

Aminocarbonylation of Aryl Halides to Produce Primary Amides by Using NH4 HCO3 Dually as Ammonia Surrogate and Base

Published:2017-10-20 Issue:22 Volume:9 Page:4206-4211
ISSN:1867-3880
Container-title:ChemCatChem
language:en
Short-container-title:ChemCatChem

Author:

Wang Dong-Liang¹,Liu Huan¹,Yang Da¹,Wang Peng¹,Lu Yong¹,Liu Ye¹^ORCID

Affiliation:

1. Shanghai Key Laboratory of Green Chemistry and Chemical Processes; School of Chemistry & Molecular Engineering; East China Normal University; 3663 North Zhongshan Road 200062 Shanghai P.R. China

Funder

the National Natural Science Foundation of China

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference37 articles.

1. Beckmann Rearrangement of Oximes under Very Mild Conditions

2. Beckmann reaction of oximes catalysed by chloral: mild and neutral procedures

3. Cyanuric Chloride as a Mild and Active Beckmann Rearrangement Catalyst

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