Literature DB >> 10814330

Lactone synthesis based on atom transfer carbonylation

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Abstract

[reaction: see text] Five- to seven-membered lactones were prepared from omega-hydroxyalkyl iodides and CO by atom transfer carbonylation without the need for transition metal catalysts. The reaction proceeds via a hybrid radical/ionic mechanism in which the intramolecular alcoholysis of an omega-hydroxyacyl iodide, arising from atom transfer carbonylation, leads to the lactone.

Entities:  

Year:  2000        PMID: 10814330     DOI: 10.1021/ol9913441

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


  2 in total

1.  A Convenient Synthetic Route to Furan Esters and Lactones by Palladium-Catalyzed Carboalkoxylation or Cyclocarbonylation of Hydroxyl-Substituted 3-Iodofurans.

Authors:  Chul-Hee Cho; Richard C Larock
Journal:  Tetrahedron Lett       Date:  2010-06-30       Impact factor: 2.415

2.  Highly substituted lactone/ester-containing furan library by the palladium-catalyzed carbonylation of hydroxyl-substituted 3-iodofurans.

Authors:  Chul-Hee Cho; Richard C Larock
Journal:  ACS Comb Sci       Date:  2011-03-24       Impact factor: 3.784

  2 in total

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