Synthesis of 2-(Cyanomethyl)benzoic Esters via Carbon–Carbon Bond Cleavage of Indanones-Reference-Cited by-同舟云学术

Synthesis of 2-(Cyanomethyl)benzoic Esters via Carbon–Carbon Bond Cleavage of Indanones

Published:2021-07-27 Issue:15 Volume:86 Page:10852-10860
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Meng Xiangtai¹,Chen Dengfeng¹,Liu Rui¹,Jiang Ping¹,Huang Shenlin¹^ORCID

Affiliation:

1. Jiangsu Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, International Innovation Center for Forest Chemicals and Materials, College of Chemical Engineering, Nanjing Forestry University, Nanjing 210037, People’s Republic of China

Funder

China Postdoctoral Science Foundation

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.1c01131

Reference49 articles.

1. New ring systems of potential carcinogenic activity. Part I. Derivatives of 4 : 9 : 10-triaza-1 : 2-5 : 6- and - 1 : 2-7 : 8-dibenzanthracene

2. Synthese des Dibenzo [b, f] chinolizidins.

3. Condensed isoquinolines. New method of synthesizing derivatives of the 5h-chromeno[2,3-c]isoquinoline system

4. Tandem Addition/Cyclization for Access to Isoquinolines and Isoquinolones via Catalytic Carbopalladation of Nitriles

5. A new method using 1,3,5-triazine as an umpolung hydrogen cyanide equivalent toward the syntheses of isoquinolinone and 2-pyridone derivatives

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