Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.tetlet.2004.06.014
Title: A highly enantioselective allyl-transfer through suppression of epimerization
Authors: Lee, C.-H.A.
Loh, T.-P. 
Keywords: Allyl transfer
Camphor
Chiral auxiliaries
Enantioselectivities
Homoallylic alcohols
Issue Date: 19-Jul-2004
Citation: Lee, C.-H.A., Loh, T.-P. (2004-07-19). A highly enantioselective allyl-transfer through suppression of epimerization. Tetrahedron Letters 45 (30) : 5819-5822. ScholarBank@NUS Repository. https://doi.org/10.1016/j.tetlet.2004.06.014
Abstract: A highly enantioselective allyl transfer method was successfully developed, producing terminal homoallylic alcohols in moderate to high yields. In all cases, reactions were carried out under mild acid conditions; reducing the reaction temperature suppressed racemization. © 2004 Elsevier Ltd. All rights reserved.
Source Title: Tetrahedron Letters
URI: http://scholarbank.nus.edu.sg/handle/10635/75427
ISSN: 00404039
DOI: 10.1016/j.tetlet.2004.06.014
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