Enantioselective synthesis of trifluoromethyl-substituted cyclopropanes.
Justin R Denton, Dinesh Sukumaran, Huw M L Davies
Index: Org. Lett. 9 , 2625, (2007)
Full Text: HTML
Abstract
The reaction of 1-aryl-2,2,2-trifluorodiazoethanes with alkenes, catalyzed by the adamantylglycine-derived dirhodium complex Rh2(R-PTAD)4, generates trifluoromethyl-substituted cyclopropanes with high diastereoselectivity (>94%) and enantioselectivity (88->98%).
Related Compounds
Related Articles:
2008-08-21
[Org. Lett. 10(16) , 3461-3, (2008)]
2010-11-01
[Eur. J. Med. Chem. 45(11) , 5080-5, (2010)]
1988-04-01
[Am. J. Physiol. 254(4 Pt 2) , F470-6, (1988)]
1992-01-01
[Toxicol. Ind. Health 8(6) , 369-76, (1992)]
2012-01-01
[Beilstein J. Org. Chem. 8 , 2223-9, (2012)]