Beilstein J. Org. Chem.2007,3, No. 24, doi:10.1186/1860-5397-3-24
of highly activated enophiles can be catalysed by H-bonding thio-ureas to give tertiary alcohols in high yields without extensive isomerisation side products. An asymmetric variant of this reaction was realised using a chiral thiourea but was limited by low enantioselectivity (up to 33% e.e.) and low
PDF
Graphical Abstract
Scheme 1:
Microwave promoted ene reaction of ethyl trifluoropyruvate with α-methyl styrene.