Literature DB >> 16524283

Pd(II)-catalyzed conversion of styrene derivatives to acetals: impact of (-)-sparteine on regioselectivity.

Amy M Balija1, Kara J Stowers, Mitchell J Schultz, Matthew S Sigman.   

Abstract

[reaction: see text] Pd[(-)-sparteine]Cl(2) catalyzes the formation of dialkyl acetals from styrene derivatives with Markovnikov regioselectivity. The substrate scope of this reaction has been investigated, and initial mechanistic studies indicate that the reaction proceeds through an enol ether intermediate and a Pd-hydride.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16524283     DOI: 10.1021/ol053110p

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


  2 in total

1.  Coupling Pd-Catalyzed Alcohol Oxidation to Olefin Functionalization: Hydrohalogenation/Hydroalkoxylation of Styrenes.

Authors:  Susanne M Podhajsky; Matthew S Sigman
Journal:  Organometallics       Date:  2007-11-05       Impact factor: 3.876

2.  A new approach to carbon-carbon bond formation: Development of aerobic Pd-catalyzed reductive coupling reactions of organometallic reagents and styrenes.

Authors:  Keith M Gligorich; Yasumasa Iwai; Sarah A Cummings; Matthew S Sigman
Journal:  Tetrahedron       Date:  2009-06-27       Impact factor: 2.457

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.