NDLI: Highly enantioselective sulfa-Michael addition reactions using N-heterocyclic carbene as a non-covalent organocatalyst† †Electronic supplementary information (ESI) available. CCDC 1047559. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c5sc00878f

Content Provider	Semantic Scholar
Author	Chen, Jiean Meng, Sixuan Wang, Leming Tang, Hongmei Huang, Yawen
Copyright Year	2015
Abstract	A triazolium salt derived NHC serves as an excellent Broensted base to promote the enantioselective carbon-sulfur bond formation in the asymmetric sulfa-Michael addition.
Starting Page	4184
Ending Page	4189
Page Count	6
File Format	PDF HTM / HTML
DOI	10.1002/chin.201543097
PubMed reference number	29218184
Volume Number	6
Alternate Webpage(s)	http://www.rsc.org/suppdata/c5/sc/c5sc00878f/c5sc00878f1.pdf
Alternate Webpage(s)	https://pubs.rsc.org/en/content/articlepdf/2015/sc/c5sc00878f
Alternate Webpage(s)	https://doi.org/10.1002/chin.201543097
Journal	Chemical Science
Language	English
Access Restriction	Open
Content Type	Text
Resource Type	Article

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