Organocatalytic asymmetric sulfa-Michael addition of thiols to trans-3,3,3-trifluoropropenyl phenyl sulfone
Stereocenter
Sulfone
Michael reaction
Tertiary amine
DOI:
10.1016/j.tetlet.2013.06.059
Publication Date:
2013-06-20T11:31:02Z
AUTHORS (4)
ABSTRACT
AbstractThe first asymmetric sulfa‐Michael addition of thiols to trans‐3,3,3‐trifluoropropenyl phenyl sulfone (I) for the construction of an unique stereogenic center bearing a trifluoromethyl group and a sulfur atom is achieved in high yields and moderate to good enantioselectivities with a chiral bifunctional amine—thiourea catalyst.
SUPPLEMENTAL MATERIAL
Coming soon ....
REFERENCES (35)
CITATIONS (20)
EXTERNAL LINKS
PlumX Metrics
RECOMMENDATIONS
FAIR ASSESSMENT
Coming soon ....
JUPYTER LAB
Coming soon ....