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REGIO AND STEREOSELECTIVE HYDROXYLATION OF 5a-HYDROXY-14-EUDESM-11-EN-3-ONE EUDESMANE BY BIOTRANSFORMATION OF RHIZOPUS NIGRICANS
(Sociedad Chilena de Química, 2006)
REGIO AND STEREOSELECTIVE HYDROXYLATION OF A-AGAROFURAN BY BIOTRANSFORMATION OF RHIZOPUS NIGRICANS
(Sociedad Chilena de Química, 2005)
BF3·OEt2-Catalyzed Unexpected Stereoselective Formation of 2,4-trans-Diallyl-2-methyl-6-aryltetrahydro-2H-pyrans with Quaternary Stereocenters
(American Chemical Society, 2021-05)
The present manuscript describes a convenient, mild, and highly stereoselective method for the allylation of δ-hydroxy-α,β-unsaturated ketones having a benzylic hydroxyl group at the δ-position using allyltrimethylsilane ...
An asymmetric substrate-controlled Morita-Baylis-Hillman reaction as approach for the synthesis of pyrrolizidinones and pyrrolizidines
(Pergamon-elsevier Science LtdOxfordInglaterra, 2014)
Highly stereoselective aldol reactions of lithium ester enolates with (Rs)-2-(p-tolylsulfinyl)cyclohexanones
(1996)
Aldol reactions lithium alkyl acetates (LiCRR″CO2R′) with (RS)-2-(p-tolylsulfinyl)cyclohexanone (1) (as an epimeric mixture at C-2) take place with very efficient control of the configuration at the tertiary hydroxylic ...
Stereo-selective activity of menthol on GABA(A) receptor
(Wiley, 2009)
alpha,beta-Unsaturated Diazoketones as Platforms in the Asymmetric Synthesis of Hydroxylated Alkaloids. Total Synthesis of 1-Deoxy-8,8a-diepicastanospermine and 1,6-Dideoxyepicastanospermine and Formal Synthesis of Pumiliotoxin 251D
(AMER CHEMICAL SOCWASHINGTON, 2012)
A versatile and concise approach for the stereoselective synthesis of mono-, di-, and trihydroxylated indolizidines is presented in four to six steps from Cbz-prolinal and a diazophosphonate. The key steps involved a Wolff ...
Site and stereoselectivity of the cyclopropanation of unsymmetrically substituted 1,3-dienes by the Simmons-Smith reaction.
(Taylor & Francis IncPhiladelphiaEUA, 1996)
Synthetic studies toward (−)-cleistenolide: highly stereoselective synthesis of new γ-lactone subunit
(Sociedade Brasileira de Química, 2022)
Synthetic Studies toward (-)-Cleistenolide: Highly Stereoselective Synthesis of New gamma-Lactone Subunits
(Sociedade Brasileira de Química, 2022)