Synthesis of tetrasubstituted alkenyl nitriles <i>via</i> cyanocarbene addition of [1.1.1]propellane-Reference-Cited by-同舟云学术

Synthesis of tetrasubstituted alkenyl nitriles via cyanocarbene addition of [1.1.1]propellane

Published:2022 Issue:8 Volume:9 Page:2234-2239
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Jiang Xinpeng¹^ORCID,Zheng Zicong²,Gao Yan¹,Lan Deyou¹,Xu Wenhao¹,Zhang Wang³,Chen Guofei³^ORCID

Affiliation:

1. College of Pharmaceutical Sciences, Zhejiang University of Technology, Hangzhou 310014, P. R. of China

2. Collaborative Innovation Center of Yangtze River Delta Region Green Pharmaceuticals, Zhejiang University of Technology, Hangzhou 310014, P.R. China

3. Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences, Ningbo 315201, People's Republic of China

Abstract

Methylenecyclobutane containing tetrasubstituted alkenyl nitriles were synthesized via strain-release driven cyanocarbene addition reaction of [1.1.1]propellane under metal-free and mild conditions.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/QO/D2QO00186A

Reference64 articles.

1. New optically active polyarylene vinylenes: control of chromophore separation by binaphthyl units

2. Oligo-2,6-naphthylenevinylenes – New Building Blocks for the Preparation of Photoluminescent Polymeric Materials

3. Nitrile-containing natural products