Literature DB >> 17385917

Rhodium-catalyzed intramolecular C-H insertion of alpha-aryl-alpha-diazo ketones.

Douglass F Taber1, Weiwei Tian.   

Abstract

Direct diazo transfer proceeds smoothly with alpha-aryl ketones. The derived alpha-aryl-alpha-diazo ketones cyclize efficiently with Rh catalysis to give the corresponding alpha-aryl cyclopentanones.

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Year:  2007        PMID: 17385917      PMCID: PMC3248813          DOI: 10.1021/jo0624694

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  15 in total

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6.  A simple method for the synthesis of substituted benzylic ketones: homologation of aldehydes via the in situ generation of aryldiazomethanes from aromatic aldehydes

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Journal:  J Org Chem       Date:  2000-10-06       Impact factor: 4.354

7.  Stereoselective preparation of a cyclopentane-based NK1 receptor antagonist bearing an unsymmetrically substituted sec-sec ether.

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Journal:  J Org Chem       Date:  2006-09-15       Impact factor: 4.354

8.  Asymmetric intermolecular C-H functionalization of benzyl silyl ethers mediated by chiral auxiliary-based aryldiazoacetates and chiral dirhodium catalysts.

Authors:  Huw M L Davies; Simon J Hedley; Brooks R Bohall
Journal:  J Org Chem       Date:  2005-12-23       Impact factor: 4.354

9.  The rearrangement of 2,3-epoxysulfonates and its application to natural products syntheses: formal synthesis of (-)-aphanorphine and total syntheses of (-)-alpha-herbertenol and (-)-herbertenediol.

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Journal:  J Org Chem       Date:  2008-09-05       Impact factor: 4.354

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Journal:  Acc Chem Res       Date:  2012-05-11       Impact factor: 22.384

3.  [3+2] Cycloaddition of alkyl aldehydes and alkynes enabled by photoinduced hydrogen atom transfer.

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Journal:  Nat Commun       Date:  2022-08-12       Impact factor: 17.694

  3 in total

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