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
Appears in Collections:Staff Publications

Show full item record
Files in This Item:
There are no files associated with this item.

SCOPUSTM   
Citations

78
checked on Dec 5, 2018

WEB OF SCIENCETM
Citations

74
checked on Nov 20, 2018

Page view(s)

141
checked on Dec 8, 2018

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.