Literature DB >> 11671990

Carbonylation of Alkynyl Epoxides: Synthesis of 5-Hydroxy-2,3-dienoate Esters and 2,3-Dihydrofuran-3-ol Derivatives.

Marcelo E. Piotti1, Howard Alper.   

Abstract

The carbonylation of alkynyl oxiranes catalyzed by (MePh(2))(4)Pd in the presence of 20 atm of carbon monoxide in methanol gives methyl 5-hydroxy-2,3-pentadienoates in good yields. When the reaction is performed on alkynyl oxiranemethanol derivatives, 4,5-dihydrofuran-3-ol derivatives are obtained stereoselectively. These products arise from the spontaneous cyclization of a dihydroxyallenyl ester intermediate.

Entities:  

Year:  1997        PMID: 11671990     DOI: 10.1021/jo971303n

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

1.  Copper-catalyzed synthesis of 2,4-disubstituted allenoates from α-diazoesters.

Authors:  Matthew Hassink; Xiaozhong Liu; Joseph M Fox
Journal:  Org Lett       Date:  2011-04-12       Impact factor: 6.005

2.  Crystal structure of (Z)-1-phenyl-3-styryl-undeca-2-en-4,10-diyn-1-ol.

Authors:  Rakesh Ganguly; Philip Wai Hong Chan
Journal:  Acta Crystallogr E Crystallogr Commun       Date:  2015-01-01
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.