Synthesis 2015; 47(22): 3611-3617
DOI: 10.1055/s-0034-1378875
paper
© Georg Thieme Verlag Stuttgart · New York

Enaminone-Based Three-Component Reactions for the Diastereoselective Synthesis of Fused Tetrahydropyridines

Jie-Ping Wan*
Key Laboratory of the Functional Small Organic Molecules, Ministry of Education, and College of Chemistry and Chemical Engineering, Jiangxi Normal University, Nanchang 330022, P. R. of China   Email: wanjieping@jxnu.edu.cn
,
Shanshan Zhong
Key Laboratory of the Functional Small Organic Molecules, Ministry of Education, and College of Chemistry and Chemical Engineering, Jiangxi Normal University, Nanchang 330022, P. R. of China   Email: wanjieping@jxnu.edu.cn
,
Yunyun Liu
Key Laboratory of the Functional Small Organic Molecules, Ministry of Education, and College of Chemistry and Chemical Engineering, Jiangxi Normal University, Nanchang 330022, P. R. of China   Email: wanjieping@jxnu.edu.cn
› Author Affiliations
Further Information

Publication History

Received: 08 May 2015

Accepted after revision: 03 July 2015

Publication Date:
14 August 2015 (online)


Abstract

An environmentally benign multicomponent synthetic method has been realized for the diastereoselective construction of fused tetrahydropyridines. Structurally diverse products have been acquired with generally good yields via the assembly of simple starting materials, enaminones or nitroenamines, o-aminophenols, and cinnamaldehydes, in the presence of lactic acid in water–ethanol media.

Supporting Information