摘要
C-Alkylation of 2-hydroxy-1,4-naphthoquinone to various nitroolefins was achieved under catalyst-free employing 'on water' conditions. The mechanism for the formation can be explained on the basis of dual activation of nitroalkene and 2-hydroxy-1,4-naphthoquinones via hydrogen bonding. Simple reaction conditions, high yields of the products, and environmentally benign medium are attractive features of this method.
原文 | 英語 |
---|---|
頁(從 - 到) | 5116-5119 |
頁數 | 4 |
期刊 | Tetrahedron Letters |
卷 | 50 |
發行號 | 36 |
DOIs | |
出版狀態 | 已發佈 - 2009 9月 9 |
ASJC Scopus subject areas
- 生物化學
- 藥物發現
- 有機化學
指紋
深入研究「Facile and highly efficient method for the C-alkylation of 2-hydroxy-1,4-naphthoquinone to nitroalkenes under catalyst-free 'on water' conditions」主題。共同形成了獨特的指紋。資料集
-
CCDC 720909: Experimental Crystal Structure Determination
Barange, D. K. (Creator), Kavala, V. (Creator), Raju, B. R. (Creator), Kuo, C. (Creator), Tseng, C. (Creator), Tu, Y. (Creator) & Yao, C. (Creator), Unknown Publisher, 2010
DOI: 10.5517/ccs6548, http://www.ccdc.cam.ac.uk/services/structure_request?id=doi:10.5517/ccs6548&sid=DataCite
資料集: Dataset