Cysteine-Derived Organocatalyst in a Highly Enantioselective Intramolecular Michael Reaction
Journal of the American Chemical Society2005Vol. 127(46), pp. 16028–16029
Citations Over TimeTop 10% of 2005 papers
Abstract
Asymmetric intramolecular Michael reaction catalyzed by an organocatalyst derived from cysteine has been developed for the synthesis of chiral bicyclo[4.3.0]nonene and cis-disubstituted cyclopentane skeletons with a creation of three or two contiguous chiral centers in good yield with high diastereo- and excellent enantioselectivities.
Related Papers
- → Theoretical investigation of atomic oxygen erosion mechanisms of 1,3-didecyl cyclopentane, 1,3-dioctyldodecyl cyclopentane and alkylated cyclopentane(2014)6 cited
- → Decomposition of cyclopentane on Ni(755): peculiar decomposition behavior of cyclopentane(1993)4 cited
- Development of extraction rectification of cyclopentane/2.2-methyl butane(2012)
- Clathrate Hydrate Capture of CO2 from Simulated Flue Gas with Cyclopentane/Water Emulsion(2010)
- Desulfidation Process of Cyclopentane(2006)