Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.tetlet.2005.08.010
Title: 1,5,7-Triazabicyclo[4.4.0]dec-5-ene (TBD) catalyzed Michael reactions
Authors: Ye, W.
Xu, J.
Tan, C.-T.
Tan, C.-H. 
Keywords: Michael reaction
Organobase
TBD
Issue Date: 3-Oct-2005
Citation: Ye, W., Xu, J., Tan, C.-T., Tan, C.-H. (2005-10-03). 1,5,7-Triazabicyclo[4.4.0]dec-5-ene (TBD) catalyzed Michael reactions. Tetrahedron Letters 46 (40) : 6875-6878. ScholarBank@NUS Repository. https://doi.org/10.1016/j.tetlet.2005.08.010
Abstract: 1,5,7-Triazabicyclo[4.4.0]dec-5-ene (TBD), a bicyclic guanidine base, has been found to be an excellent catalyst for Michael and Michael-type reactions. A wide variety of Michael donors and acceptors can participate in these reactions using 10-20 mol % of TDB. These reactions are mild, fast, easy to perform, produce excellent yields and can occur in several solvents without the need for strictly anhydrous conditions. © 2005 Elsevier Ltd. All rights reserved.
Source Title: Tetrahedron Letters
URI: http://scholarbank.nus.edu.sg/handle/10635/75391
ISSN: 00404039
DOI: 10.1016/j.tetlet.2005.08.010
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