Literature DB >> 11457407

A new class of chiral lewis acid catalysts for highly enantioselective hetero-Diels-Alder reactions: exceptionally high turnover numbers from dirhodium(II) carboxamidates.

M P Doyle1, I M Phillips, W Hu.   

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Year:  2001        PMID： 11457407     DOI： 10.1021/ja015692l

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN： 0002-7863            Impact factor:   15.419


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  6 in total

1.  Examination of the mechanism of Rh(2)(II)-catalyzed carbazole formation using intramolecular competition experiments.

Authors:  Benjamin J Stokes; Kathleen J Richert; Tom G Driver
Journal:  J Org Chem       Date:  2009-09-04       Impact factor: 4.354

2.  Perspective on dirhodium carboxamidates as catalysts.

Authors:  Michael P Doyle
Journal:  J Org Chem       Date:  2006-12-08       Impact factor: 4.354

3.  Dihydropyranone formation by ipso C-H activation in a glucal 3-carbamate-derived rhodium acyl nitrenoid.

Authors:  Brisa Hurlocker; Nadia C Abascal; Lindsay M Repka; Elsy Santizo-Deleon; Abigail L Smenton; Victoria Baranov; Ritu Gupta; Sarah E Bernard; Shenjuti Chowdhury; Christian M Rojas
Journal:  J Org Chem       Date:  2011-03-07       Impact factor: 4.354

4.  Solvent enhancement of reaction selectivity: a unique property of cationic chiral dirhodium carboxamidates.

Authors:  Xiaochen Wang; Carolin Weigl; Michael P Doyle
Journal:  J Am Chem Soc       Date:  2011-05-27       Impact factor: 15.419

5.  Asymmetric hetero-Diels-Alder reaction catalyzed by dirhodium(II) carboxamidates.

Authors:  Michael P Doyle; Marcela Valenzuela; Penglin Huang
Journal:  Proc Natl Acad Sci U S A       Date:  2004-04-01       Impact factor: 11.205

6.  High Symmetry Dirhodium(II) Paddlewheel Complexes as Chiral Catalysts.

Authors:  Jørn Hansen; Huw M L Davies
Journal:  Coord Chem Rev       Date:  2008-03       Impact factor: 22.315
  6 in total

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