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  4. Synthesis of Hydroxylated 3,4-Dihydropyridine-2-ones from Intramolecular Nucleophilic Addition Reaction of Oxirane-containing Tertiary Enamides
 
research article

Synthesis of Hydroxylated 3,4-Dihydropyridine-2-ones from Intramolecular Nucleophilic Addition Reaction of Oxirane-containing Tertiary Enamides

Yang, Luo
•
Tong, Shuo  
•
Wang, De-Xian
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2011
Synlett

Catalyzed by p-toluenesulfonic acid in dry acetonitrile, oxirane-containing tertiary enamides underwent efficient cyclization via intramolecular addition to produce 3-hydroxy-3,4-dihydropyridin-2(1H)-one derivatives in moderate to good yields.

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Type
research article
DOI
10.1055/s-0030-1259703
Web of Science ID

WOS:000289411900013

Author(s)
Yang, Luo
Tong, Shuo  
Wang, De-Xian
Huang, Zhi-Tang
Zhu, Jieping  
Wang, Mei-Xiang
Date Issued

2011

Publisher

Georg Thieme Verlag

Published in
Synlett
Issue

7

Start page

927

End page

930

Subjects

enamides, oxiranes, nucleophilic addition, cyclization, 3,4-dihydropyridin-2-ones

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LSPN  
Available on Infoscience
April 30, 2011
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/66926
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