Literature DB >> 18726011

Synthetic applications of carbolithiation transformations.

Anne-Marie L Hogan1, Donal F O'Shea.   

Abstract

Carbolithiation reactions are exceptionally versatile transformations which have been utilised in a remarkably diverse and creative manner. In this review we outline the background and scope of these reactions and then focus on their use in organic synthesis with a particular emphasis on literature examples published since 2000.

Year:  2008        PMID： 18726011     DOI： 10.1039/b805595e

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN： 1359-7345            Impact factor:   6.222


  5 in total

Review 1.  Regio- and stereoselective intermolecular carbolithiation reactions.

Authors:  G Marsico; P Scafato; S Belviso; S Superchi
Journal:  RSC Adv       Date:  2020-09-02       Impact factor: 4.036

2.  Enantioselective one-carbon expansion of aromatic rings by simultaneous formation and chromoselective irradiation of a transient coloured enolate.

Authors:  Rakesh K Saunthwal; James Mortimer; Andrew J Orr-Ewing; Jonathan Clayden
Journal:  Chem Sci       Date:  2022-01-25       Impact factor: 9.825

3.  Intramolecular carbonickelation of alkenes.

Authors:  Rudy Lhermet; Muriel Durandetti; Jacques Maddaluno
Journal:  Beilstein J Org Chem       Date:  2013-04-12       Impact factor: 2.883

4.  Inter- and intramolecular enantioselective carbolithiation reactions.

Authors:  Asier Gómez-Sanjuan; Nuria Sotomayor; Esther Lete
Journal:  Beilstein J Org Chem       Date:  2013-02-13       Impact factor: 2.883

5.  Carbolithiation of N-alkenyl ureas and N-alkenyl carbamates.

Authors:  Julien Lefranc; Alberto Minassi; Jonathan Clayden
Journal:  Beilstein J Org Chem       Date:  2013-03-28       Impact factor: 2.883
  5 in total

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