Please use this identifier to cite or link to this item: https://doi.org/10.1021/ja104168q
Title: Facile, efficient, and catalyst-free electrophilic aminoalkoxylation of olefins: Scope and application
Authors: Zhou, L.
Tan, C.K.
Zhou, J.
Yeung, Y.-Y. 
Issue Date: 4-Aug-2010
Source: Zhou, L.,Tan, C.K.,Zhou, J.,Yeung, Y.-Y. (2010-08-04). Facile, efficient, and catalyst-free electrophilic aminoalkoxylation of olefins: Scope and application. Journal of the American Chemical Society 132 (30) : 10245-10247. ScholarBank@NUS Repository. https://doi.org/10.1021/ja104168q
Abstract: A new one-pot electrophilic aminoalkoxylation reaction using olefin, cyclic ether, amine, and N-bromosuccinimide has been developed. The olefinic substrates and the cyclic ether partners can be flexibly varied to produce a range of amino ether derivatives. This novel protocol has been applied in the facile and efficient synthesis of biologically active morpholine compounds. © 2010 American Chemical Society.
Source Title: Journal of the American Chemical Society
URI: http://scholarbank.nus.edu.sg/handle/10635/76169
ISSN: 00027863
DOI: 10.1021/ja104168q
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