Literature DB >> 24394608

Regioselective functionalization of 2-arylazetidines: evaluating the ortho-directing ability of the azetidinyl ring and the α-directing ability of the N-substituent.

Leonardo Degennaro1, Marina Zenzola, Piera Trinchera, Laura Carroccia, Arianna Giovine, Giuseppe Romanazzi, Aurelia Falcicchio, Renzo Luisi.   

Abstract

The regioselective lithiation-functionalization of 2-arylazetidines has been explored. The nature of the N-substituent is mainly responsible for a regioselectivity switch. ortho-Lithiation occurred, using hexyllithium as a greener base, in N-alkylazetidines, while α-benzylic lithiation has been observed with N-Boc azetidines.

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Year:  2014        PMID: 24394608     DOI: 10.1039/c3cc48555b

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


  2 in total

1.  Dynamic Phenomena and Complexation Effects in the α-Lithiation and Asymmetric Functionalization of Azetidines.

Authors:  Pantaleo Musci; Marco Colella; Angela Altomare; Giuseppe Romanazzi; Nadeem S Sheikh; Leonardo Degennaro; Renzo Luisi
Journal:  Molecules       Date:  2022-04-29       Impact factor: 4.927

2.  Stereo- and Enantioselective Addition of Organolithiums to 2-Oxazolinylazetidines as a Synthetic Route to 2-Acylazetidines.

Authors:  Pantaleo Musci; Marco Colella; Flavio Fanelli; Angela Altomare; Luisa Pisano; Claudia Carlucci; Renzo Luisi; Leonardo Degennaro
Journal:  Front Chem       Date:  2019-09-10       Impact factor: 5.221

  2 in total

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