Literature DB >> 22070857

Synthesis of a new class of β-iodo N-alkenyl 2-pyridones.

Sarah Z Tasker1, Benjamin M Brandsen, Keun Ah Ryu, Gregory S Snapper, Richard J Staples, Roger L DeKock, Carolyn E Anderson.   

Abstract

A new method for the synthesis of β-iodo N-alkenyl 2-pyridones from substituted 2-propargyloxypyridines has been discovered . These compounds present a unique complement of orthogonal functionality and structural characteristics that are unavailable via other routes. The ready access to these compounds renders them an important entry point for the preparation of more complex N-alkyl pyridone-containing targets.

Entities:  

Year:  2011        PMID: 22070857     DOI: 10.1021/ol202679t

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Enantioselective propargylic [1,3]-rearrangements: copper-catalyzed O-to-N migrations toward C-N bond formation.

Authors:  Li-Jie Cheng; Alexander P N Brown; Christopher J Cordier
Journal:  Chem Sci       Date:  2017-03-31       Impact factor: 9.825

2.  Rhodium-NHC-Catalyzed gem-Specific O-Selective Hydropyridonation of Terminal Alkynes.

Authors:  María Galiana-Cameo; Raúl Romeo; Asier Urriolabeitia; Vincenzo Passarelli; Jesús J Pérez-Torrente; Victor Polo; Ricardo Castarlenas
Journal:  Angew Chem Int Ed Engl       Date:  2022-03-19       Impact factor: 16.823

  2 in total

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