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Acid-catalyzed tandem reaction for the synthesis of pyridine derivatives via CC/C(sp3)–N bond cleavage of enones and primary amines†
Zhong-Yuan Mao,Xiao-Yun Liao,Heng-Shan Wang,Chun-Gu Wang,Ke-Bin Huang,Ying-Ming Pan
RSC Advances Pub Date : 02/24/2017 00:00:00 , DOI:10.1039/C7RA00780A
Abstract

A one-pot acid-catalyzed tandem reaction has been developed without any metallic reagents or extra oxidants. This reaction involves a C[double bond, length as m-dash]C bond cleavage of enones via a “masked” reverse Aldol reaction, and C(sp3)–N bond cleavage of primary amines to provide nitrogen sources for the assembly of pyridine derivatives in high yields with excellent functional group tolerance.

Graphical abstract: Acid-catalyzed tandem reaction for the synthesis of pyridine derivatives via C [[double bond, length as m-dash]] C/C(sp3)–N bond cleavage of enones and primary amines
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