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AgNTf2 catalyzed cycloaddition of N-acyliminium ions with alkynes for the synthesis of the 3,4-dihydro-1,3-oxazin-2-one skeleton.
Xu, Wen-Ke; Guo, Jia-Ming; Liu, Chang-Hong; Sun, Jian-Ting; Lv, Min; Wei, Bang-Guo.
Afiliación
  • Xu WK; Department of Natural Medicine, School of Pharmacy, Fudan University, 826 Zhangheng Road, Shanghai 201203, China. bgwei1974@fudan.edu.cn.
  • Guo JM; Department of Natural Medicine, School of Pharmacy, Fudan University, 826 Zhangheng Road, Shanghai 201203, China. bgwei1974@fudan.edu.cn.
  • Liu CH; Department of Natural Medicine, School of Pharmacy, Fudan University, 826 Zhangheng Road, Shanghai 201203, China. bgwei1974@fudan.edu.cn.
  • Sun JT; Department of Natural Medicine, School of Pharmacy, Fudan University, 826 Zhangheng Road, Shanghai 201203, China. bgwei1974@fudan.edu.cn.
  • Lv M; Department of Natural Medicine, School of Pharmacy, Fudan University, 826 Zhangheng Road, Shanghai 201203, China. bgwei1974@fudan.edu.cn.
  • Wei BG; Department of Natural Medicine, School of Pharmacy, Fudan University, 826 Zhangheng Road, Shanghai 201203, China. bgwei1974@fudan.edu.cn.
Org Biomol Chem ; 20(25): 5086-5094, 2022 06 29.
Article en En | MEDLINE | ID: mdl-35698865
ABSTRACT
A catalyzed process for the synthesis of the 4,6-substituted 3,4-dihydro-1,3-oxazin-2-one skeleton has been developed through cycloaddition of in situ generated acyliminium intermediates with alkynes. A range of chain N,O-acetals and terminal alkynes were amenable for this mild transformation. As a result, a series of desired cycloaddition products were obtained in moderate to good yields.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Esqueleto / Alquinos Idioma: En Revista: Org Biomol Chem Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2022 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Esqueleto / Alquinos Idioma: En Revista: Org Biomol Chem Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2022 Tipo del documento: Article País de afiliación: China
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