Momentary click nitrile synthesis enabled by an aminoazanium reagent-Reference-Cited by-同舟云学术

Momentary click nitrile synthesis enabled by an aminoazanium reagent

Published:2022 Issue:13 Volume:9 Page:3420-3427
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Xu Liangxuan¹²,Hu Yue¹,Zhu Xiang¹^ORCID,He Lin¹^ORCID,Wu Qing³,Li Chen³,Xia Chungu¹,Liu Chao¹^ORCID

Affiliation:

1. State Key Laboratory for Oxo Synthesis and Selective Oxidation & CAS Key Laboratory of Chemistry of Northwestern Plant Resources, Suzhou Research Institute, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou 730000, China

2. University of Chinese Academy of Sciences, Beijing 100049, China

3. China National Offshore Oil Corporation, Beijing 100010, China

Abstract

By using a robust aminoazanium reagent H2N-DABCO, a momentary clicking nitrile synthesis from aldehyde and various adehyde precursors was achieved.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Jiangsu Province

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/QO/D2QO00560C

Reference52 articles.

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2. Nitrile-Containing Pharmaceuticals: Efficacious Roles of the Nitrile Pharmacophore

3. HCl·DMPU-assisted one-pot and metal-free conversion of aldehydes to nitriles

4. Sulfuryl Fluoride Mediated Conversion of Aldehydes to Nitriles

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