Literature DB >> 15771469

New phosphite-oxazoline ligands for efficient Pd-catalyzed substitution reactions.

Oscar Pàmies1, Montserrat Diéguez, Carmen Claver.   

Abstract

We have designed and synthesized a new family of readily available highly modular phosphite-oxazoline ligands for the Pd-catalyzed asymmetric allylic substitution reactions. The introduction of a pi-acceptor flexible bulky biphenyl phosphite moiety in the ligand design is highly adventitious in the product outcome. Thus, this ligand series affords excellent reaction rates (TOF's up to >2400 mol.(mol.h)-1) and enantioselectivities (ee's up to >99%) and, at the same time, shows a broad scope for different substrate types.

Entities:  

Year:  2005        PMID: 15771469     DOI: 10.1021/ja0425738

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


  5 in total

1.  Iridium-catalyzed kinetic asymmetric transformations of racemic allylic benzoates.

Authors:  Levi M Stanley; Chen Bai; Mitsuhiro Ueda; John F Hartwig
Journal:  J Am Chem Soc       Date:  2010-07-07       Impact factor: 15.419

2.  Origins of Regioselectivity in Iridium Catalyzed Allylic Substitution.

Authors:  Sherzod T Madrahimov; Qian Li; Ankit Sharma; John F Hartwig
Journal:  J Am Chem Soc       Date:  2015-11-20       Impact factor: 15.419

3.  A superior P-H phosphonite: asymmetric allylic substitutions with fenchol-based palladium catalysts.

Authors:  Bernd Goldfuss; Thomas Löschmann; Tina Kop-Weiershausen; Jörg Neudörfl; Frank Rominger
Journal:  Beilstein J Org Chem       Date:  2006-03-30       Impact factor: 2.883

4.  Allylic alkylations catalyzed by palladium-bis(oxazoline) complexes derived from heteroarylidene malonate derivatives.

Authors:  Lei Liu; Hongli Ma; Bin Fu
Journal:  Molecules       Date:  2012-02-17       Impact factor: 4.411

5.  Synthesis of 1-[bis(trifluoromethyl)phosphine]-1'-oxazolinylferrocene ligands and their application in regio- and enantioselective Pd-catalyzed allylic alkylation of monosubstituted allyl substrates.

Authors:  Zeng-Wei Lai; Rong-Fei Yang; Ke-Yin Ye; Hongbin Sun; Shu-Li You
Journal:  Beilstein J Org Chem       Date:  2014-05-30       Impact factor: 2.883

  5 in total

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