Literature DB >> 12568600

Synthesis and aldol reactivity of o- and C-enolate complexes of nickel.

Juan Cámpora1, Celia M Maya, Pilar Palma, Ernesto Carmona, Enrique Gutiérrez-Puebla, Caridad Ruiz.   

Abstract

The often facile C-/O-tautomerization of transition metal enolates is severely hindered in the cyclic Ni complexes 1 and 2, allowing the study of their individual reactivities. At room temperature only the O-bound tautomer, 2, reacts with aldehydes, giving rise to the corresponding addition products.

Entities:  

Year:  2003        PMID: 12568600     DOI: 10.1021/ja028711f

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


  3 in total

1.  Mo-catalyzed regio-, diastereo-, and enantioselective allylic alkylation of 3-aryloxindoles.

Authors:  Barry M Trost; Yong Zhang
Journal:  J Am Chem Soc       Date:  2007-11-07       Impact factor: 15.419

2.  Suzuki-Miyaura coupling of arylboronic acids to gold(iii).

Authors:  Ayan Maity; Amanda N Sulicz; Nihal Deligonul; Matthias Zeller; Allen D Hunter; Thomas G Gray
Journal:  Chem Sci       Date:  2014-11-06       Impact factor: 9.825

3.  Ag2O nanoparticle-catalyzed substrate-controlled regioselectivities: direct access to 3-ylidenephthalides and isocoumarins.

Authors:  Sandeep Chaudhary; Bharti Rajesh K Shyamlal; Lalit Yadav; Mohit K Tiwari; Krishan Kumar
Journal:  RSC Adv       Date:  2018-06-26       Impact factor: 4.036

  3 in total

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