Triruthenium dodecacarbonyl/triphenylphosphine catalyzed dehydrogenation of primary and secondary alcohols

被引:36
作者
Meijer, RH
Ligthart, GBWL
Meuldijk, J
Vekemans, JAJM
Hulshof, LA
Mills, AM
Kooijman, H
Spek, AL
机构
[1] Eindhoven Univ Technol, Lab Macromol & Organ Chem, NL-5600 MB Eindhoven, Netherlands
[2] Eindhoven Univ Technol, Proc Dev Grp, NL-5600 MB Eindhoven, Netherlands
[3] Univ Utrecht, Bijvoet Ctr Biomol Res Crystal & Struct Chem, NL-3584 CH Utrecht, Netherlands
关键词
triruthenium dodecacarbonyl catalyst; catalytic dehydrogenation; alcohols; ligands; hydride acceptors;
D O I
10.1016/j.tet.2003.11.082
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Dehydrogenation of alcohols into aldehydes and ketones by Ru-3(CO)(12)/PPh3 based homogeneous catalysis has been investigated as an alternative for the classical Oppenauer oxidation. Several catalytic systems have been screened in the Oppenauer-like oxidation of alcohols. A systematic study of various combinations of Ru-3(CO)(12), mono- and bidentate ligands and hydride acceptors was performed to enable dehydrogenation of primary alcohols to stop at the aldehyde stage. Among many H-acceptors screened, diphenylacetylene (tolane) proved the most suitable judged from its smooth reduction. Electron rich and deficient analogues of tolane have been synthesized and, based on competition experiments between these H-acceptors, a tentative catalytic cycle for the Ru-3(CO)(12)/PPh3-catalyzed dehydrogenations has been proposed. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1065 / 1072
页数:8
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