期刊
TETRAHEDRON LETTERS
卷 41, 期 10, 页码 1601-1605出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0040-4039(99)02339-4
关键词
asymmetric reactions; catalysis; ketones; reduction
A new methodology for the catalytic enantioselective reduction of oc-alkoxy-ketones is described. The procedure employes Zn(OTf)(2)-bis-oxazoline complexes (8-10 mol%) as catalysts and catecholborane as the reducing agent. The reaction, carried out in CH2Cl2 at 0 degrees C, affords the alpha-alkoxy-alcohols in high yields and with good enantioselectivity. (C) 2000 Elsevier Science Ltd. All rights reserved.
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