Literature DB >> 22474004

Base-catalyzed direct aldolization of α-alkyl-α-hydroxy trialkyl phosphonoacetates.

Michael T Corbett1, Daisuke Uraguchi, Takashi Ooi, Jeffrey S Johnson.   

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Year:  2012        PMID: 22474004      PMCID: PMC3685868          DOI: 10.1002/anie.201200559

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


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  38 in total

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5.  Catalytic silicon-mediated carbon-carbon bond-forming reactions of unactivated amides.

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7.  High facial diastereoselectivity in intra- and intermolecular reactions of chiral benzylic cations.

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8.  Studies on new phosphate ester antifungal antibiotics phoslactomycins. II. Structure elucidation of phoslactomycins A to F.

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9.  Chiral tetraaminophosphonium carboxylate-catalyzed direct Mannich-type reaction.

Authors:  Daisuke Uraguchi; Yusuke Ueki; Takashi Ooi
Journal:  J Am Chem Soc       Date:  2008-10-04       Impact factor: 15.419

10.  Magnesium-catalyzed asymmetric direct aldol addition of ethyl diazoacetate to aromatic, aliphatic, and alpha,beta-unsaturated aldehydes.

Authors:  Barry M Trost; Sushant Malhotra; Benjamin A Fried
Journal:  J Am Chem Soc       Date:  2009-02-11       Impact factor: 15.419

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3.  Phosphite-Mediated Reductive Cross-Coupling of Isatins and Nitrostyrenes.

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4.  Dynamic kinetic asymmetric transformations of β-stereogenic α-ketoesters by direct aldolization.

Authors:  Michael T Corbett; Jeffrey S Johnson
Journal:  Angew Chem Int Ed Engl       Date:  2013-11-12       Impact factor: 15.336

5.  Phosphazene-catalyzed desymmetrization of cyclohexadienones by dithiane addition.

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6.  Enantioselective bifunctional iminophosphorane catalyzed sulfa-Michael addition of alkyl thiols to unactivated β-substituted-α,β-unsaturated esters.

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7.  Bifunctional iminophosphorane organocatalysts for enantioselective synthesis: application to the ketimine nitro-Mannich reaction.

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8.  Structure-Activity Relationship Studies of Cyclopropenimines as Enantioselective Brønsted Base Catalysts.

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  8 in total

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