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Organocatalysis.org | organocatalysis.org Reviews
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Iminium Catalysis : Organocatalysis.org
http://www.organocatalysis.org/category/iminium-catalysis
Archive by category Iminium Catalysis. New Strategies for Organic Catalysis: The First Highly Enantioselective Organocatalytic Diels-Alder Reaction. September 17, 2008. Kateri A. Ahrendt, Christopher J. Borths, and David W. C. MacMillan*. J Am Chem. Soc. 122 (17), 4243 -4244 (. Macmillan and co-workers report the first highly enantioselective organocatalytic Diels-Alder reaction. By the use of a novel imidazolidinone catalysts, the cycloaddition product 4. September 11, 2008. 67 (24), 8331 -8338, 2002.
Dienamine-Jorgensen : Organocatalysis.org
http://www.organocatalysis.org/category/dienamine-catalysis/dienamine-jorgensen
Archive by category Dienamine Catalysis. Dienamine Catalysis: Organocatalytic Asymmetric γ-Amination of α,β-Unsaturated Aldehydes. June 11, 2008. Peter Dinér, and. J Am Chem. Soc.,. 39), 12973 -12980, 2006; DOI:. Jørgensen and co-workers have reported the first organocatalytic enantioselective. Unsaturated aldehydes. They disclosed that secondary amines, and in particular. 2-[bis(3,5-bistrifluoromethylphenyl)trimethyl-silanyloxymethyl]pyrrolidine, can invert the common reactivity of.
Chiral Thiourea Catalysis : Organocatalysis.org
http://www.organocatalysis.org/category/chiral-thiourea-catalysis
Archive by category Chiral Thiourea Catalysis. Enantioselective Hydroxylation of Nitroalkenes: An Organocatalytic Approach. June 25, 2008. Peter Dinér, Martin Nielsen, Søren Bertelsen, Barbara Niess and Karl Anker Jørgensen*. 2007(35), 3646 - 3648. The transformation of the nitro alkenes proceeded easily in good yields (63-82%) and good enantioselectivity (89-93%). Received May 3, 2007, June 13, 2007, DOI:. Written by admin · Filed Under Chiral Thiourea Catalysis. Middot; Organic Chemistry Portal ·.
Enamine-chemistry : Organocatalysis.org
http://www.organocatalysis.org/category/enamine-catalysis/enamine-chemistry
Archive by category Enamine Catalysis. On the Origin of the Stereoselectivity in Organocatalysed Reactions with TMS-Protected Diarylprolinol. July 17, 2008. Peter Dinér, Anne Kjærsgaard, Mette Alstrup Lie, and Karl Anker Jørgensen*. Chem Eur. J. 14, 122 127. Jørgensen and co-workers investigate computationally the transition states involved in the stereoselective electrophilic α-fluorination of aldehydes with N-fluorobenzenesulfonimide (NFSI) as the fluorination reagent.
Enantioselective Organocatalysis : Organocatalysis.org
http://www.organocatalysis.org/organocatalysis
David W. C. Macmillan. Sign up to receive the latest news and updates from this site! Middot; Organic Chemistry Portal ·.
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Organocatalysis.org
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