Synthesis of Multisubstituted Guanidines through Palladium-Catalyzed Insertion of Isonitriles-Reference-Cited by-同舟云学术

Synthesis of Multisubstituted Guanidines through Palladium-Catalyzed Insertion of Isonitriles

Published:2018-09-26 Issue:17 Volume:29 Page:2326-2330
ISSN:0936-5214
Container-title:Synlett
language:en
Short-container-title:Synlett

Author:

Yang Li¹,Tang Hai-Tao²,Li Pei-Xia²,Meng Xiu-Jin²,Pan Ying-Ming²

Affiliation:

1. Guangxi Key Laboratory of Special Non-wood Forest Cultivation and Utilization, Guangxi Zhuang Autonomous Region Forestry Research Institute

2. State Key Laboratory for the Chemistry and Molecular Engineering of Medicinal Resources, School of Chemistry and Pharmaceutical Sciences of Guangxi Normal University

Abstract

A new method for the synthesis of multisubstituted guanidines through tandem intermolecular insertion of isonitriles with unactivated amides has been developed. In this study, isonitriles could be used not only as reaction materials but also as the source of amines.

Funder

National Natural Science Foundation of China

Publisher

Georg Thieme Verlag KG

Subject

Organic Chemistry

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0037-1610981.pdf

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4. Synthesis and Characterization of Aryl Acylguanidines and Their Copper(II) Complexes;CHINESE J STRUC CHEM;2019