An efficient route to a 5,6-dihydropyrano[3,4-b]pyridin-8-one core in two steps from enaminolactones
摘要:
A convenient two step conversion of heterocyclic enaminolactones to heterocyclic fused 2-pyran-1-ones is reported. The use of this method can be applied to a wide variety of aromatic and heteroaromatic amines to give potentially biologically active compounds in good yields. (c) 2007 Elsevier Ltd. All rights reserved.
Zhang, Zhan-Hui; Song, Li-Ming, Journal of Chemical Research, 2005, # 12, p. 817 - 820
作者:Zhang, Zhan-Hui、Song, Li-Ming
DOI:——
日期:——
An efficient route to a 5,6-dihydropyrano[3,4-b]pyridin-8-one core in two steps from enaminolactones
作者:Cheikh Sall、Nicolas Desbois、Sandrine Paquelet、José R. Camacho、Jean Michel Chezal、Jean-Claude Teulade、Yves Blache
DOI:10.1016/j.tetlet.2007.12.106
日期:2008.2
A convenient two step conversion of heterocyclic enaminolactones to heterocyclic fused 2-pyran-1-ones is reported. The use of this method can be applied to a wide variety of aromatic and heteroaromatic amines to give potentially biologically active compounds in good yields. (c) 2007 Elsevier Ltd. All rights reserved.
Enaminones as potential prodrugs of primary and secondary amines
申请人:Merck & Co., Inc.
公开号:EP0214009A3
公开(公告)日:1989-01-11
Novel enzymatically labile enaminones useful as potential prodrugs of primary and secondary amines are disclosed. Also, disclosed herein are compositions comprising said amines and methods of administering said composition to warm-blooded animals.