Facile, efficient, and catalyst-free electrophilic aminoalkoxylation of olefins: Scope and application

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
Citation:	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
Appears in Collections:	Staff Publications

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