AgOTf-catalyzed cyclization of enynals or enynones with amines: An efficient synthesis of 1,2,4-trisubstituted pyrroles and 2,3,5-trisubstituted furans

Arkivoc

Volumn 2011, Issue 9, 2011, Pages 381-392

  Chen, Wan Li ^a   Li, Jiao ^a   Zhu, Ying Hong ^a   Ye, Lu Ting ^a   Hu, Wei ^a   Mo, Wei Min ^a  

^a ZHEJIANG UNIVERSITY OF TECHNOLOGY   (China)

Author keywords

1,2,4 trisubstituted pyrroles; 2,3,5 trisubstituted furans; AgOTf; Amino cyclization; Enynals; Enynones

Indexed keywords

EID: 79960208215     PISSN: 1551-7012     EISSN: 15517004     Source Type: Journal    
DOI: 10.3998/ark.5550190.0012.928     Document Type: Article

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69. This may due to the sterically hindered of the substrate between aldehyde and ketone. The condensation reaction between aldehyde and arylamine affords the imine is more faster.