Literature DB >> 10814370

Parallel kinetic resolution of racemic aldehydes by use of asymmetric Horner-Wadsworth-Emmons reactions

.   

Abstract

[reaction: see text] A racemic aldehyde can undergo parallel kinetic resolution (PKR) by simultaneous reaction with two different chiral phosphonates, differing either in the structure of the chiral auxiliary or in the structure of the phosphoryl group (i.e., one (E)- and one (Z)-selective reagent). This strategy allows conversion of a racemic aldehyde to two different, synthetically useful chiral products with essentially doubled material throughput and similar or improved selectivities as compared to conventional kinetic resolution.

Entities:  

Year:  2000        PMID: 10814370     DOI: 10.1021/ol991387h

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  Catalytic parallel kinetic resolution under homogeneous conditions.

Authors:  Trisha A Duffey; James A Mackay; Edwin Vedejs
Journal:  J Org Chem       Date:  2010-07-16       Impact factor: 4.354

2.  Synthesis of (R)-3,4-dihydro-2H-pyran-2-carboxaldehyde: application to the synthesis of potent adenosine A(2A) and A(3) receptor agonist.

Authors:  Prakash G Jagtap; Zhiyu Chen; Karsten Koppetsch; Elizabeth Piro; Paula Fronce; Garry J Southan; Karl-Norbert Klotz
Journal:  Tetrahedron Lett       Date:  2009-06-03       Impact factor: 2.415

3.  Desymmetrization of enone-diones via rhodium-catalyzed diastereo- and enantioselective tandem conjugate addition-aldol cyclization.

Authors:  Brian M Bocknack; Long-Cheng Wang; Michael J Krische
Journal:  Proc Natl Acad Sci U S A       Date:  2004-03-15       Impact factor: 11.205

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.