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Diastereo- and enantioselective synthesis of a conagenin skeletal amide moiety
(Pergamon-elsevier Science LtdOxfordInglaterra, 2004)
Theoretical studies of the asymmetric alkylation reaction on chiral enamines
(Elsevier Science BvAmsterdamHolanda, 2005)
A chemoenzymatic synthesis of the sex pheromone of Lasioderma serricorne F.
(Soc Brasileira QuimicaSao PauloBrasil, 1998)
Ozonolysis of Morita-Baylis-Hillman adducts originated from aromatic aldehydes: an expeditious diastereoselective approach for the preparation of alpha,beta-dihydroxy-esters
(Pergamon-elsevier Science LtdOxfordInglaterra, 2008)
A highly enantioselective chemoenzymatic synthesis of syn-3-amino-2-hydroxy esters: key intermediates for taxol side chain and phenylnorstatine
(Pergamon-elsevier Science LtdOxfordInglaterra, 2005)
Palladium catalyzed Heck reaction of arenediazonium tetrafluoroborate salts with Baylis-Hillman adducts: production of alpha-benzyl-beta-keto esters
(Pergamon-elsevier Science LtdOxfordInglaterra, 2006)
Chemoenzymatic Synthesis of alpha-Hydroxy-beta-methyl-gamma-hydroxy Esters: Role of the Keto-Enol Equilibrium To Control the Stereoselective Hydrogenation in a Key Step
(Amer Chemical Soc, 2010-03-05)
alpha-Hydroxy-beta-methyl-gamma-hydroxy esters not only are found in many natural products and potent drugs but also are useful intermediates in organic synthesis due to their highly functionalized skeleton that can be ...
Chemoenzymatic Synthesis of alpha-Hydroxy-beta-methyl-gamma-hydroxy Esters: Role of the Keto-Enol Equilibrium To Control the Stereoselective Hydrogenation in a Key Step
(Amer Chemical Soc, 2010-03-05)
alpha-Hydroxy-beta-methyl-gamma-hydroxy esters not only are found in many natural products and potent drugs but also are useful intermediates in organic synthesis due to their highly functionalized skeleton that can be ...