Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/23024
Title: Base-accelerated enantioselective substitution of morita-baylis-hillman carbonates with dialkyl phosphine oxides
Authors: Sun, W
Hong, L
Liu, C
Wang, R
Issue Date: 2010
Publisher: American Chemical Society
Source: Organic letters, 2010, v. 12, no. 17, p. 3914-3917 How to cite?
Journal: Organic letters 
Abstract: A base could accelerate the SN2′ or SN2′- SN2′ reaction of Morita-Baylis-Hillman (MBH) carbonates with dialkyl phosphine oxides, but the judicial choice of an appropriate base would greatly depress this competitive SN2′ reaction and allow for a highly enantioselective allylic substitution reaction with satisfactory yields and excellent enantioselectivities.
URI: http://hdl.handle.net/10397/23024
ISSN: 1523-7060
EISSN: 1523-7052
DOI: 10.1021/ol101601d
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