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Azide-Enolate Cycloaddition-Rearrangement Enables Direct α-Amination of Amides and Enelactam Synthesis from Esters.
Bell-Tyrer, Joseph J; Hume, Paul A; Grant, Phillip S; Brimble, Margaret A; Furkert, Daniel P.
Afiliação
  • Bell-Tyrer JJ; School of Chemical Sciences and, Maurice Wilkins Centre for Molecular Biodiscovery, The University of Auckland, 23 Symonds St, Auckland, 1010, New Zealand.
  • Hume PA; School of Chemical & Physical Sciences, Victoria University of Wellington, Kelburn Parade, Wellington, 6012, New Zealand.
  • Grant PS; School of Chemical Sciences and, Maurice Wilkins Centre for Molecular Biodiscovery, The University of Auckland, 23 Symonds St, Auckland, 1010, New Zealand.
  • Brimble MA; School of Chemical Sciences and, Maurice Wilkins Centre for Molecular Biodiscovery, The University of Auckland, 23 Symonds St, Auckland, 1010, New Zealand.
  • Furkert DP; School of Chemical Sciences and, Maurice Wilkins Centre for Molecular Biodiscovery, The University of Auckland, 23 Symonds St, Auckland, 1010, New Zealand.
Chemistry ; 29(31): e202301235, 2023 Jun 02.
Article em En | MEDLINE | ID: mdl-37166050
ABSTRACT
Invited for the cover of this issue are Dan Furkert, Joe Bell-Tyrer and co-workers at the University of Auckland and Victoria University of Wellington. The image depicts a tandem cycloaddition-rearrangement process delivering a diverse range of molecular frameworks from simple precursors. Read the full text of the article at 10.1002/chem.202300261.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Chemistry Ano de publicação: 2023 Tipo de documento: Article
Texto completo
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PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Chemistry Ano de publicação: 2023 Tipo de documento: Article