Literature DB >> 18671429

An efficient method for the synthesis of vinylbromohydrin and vinylbromoalkoxy derivatives and cyclocarbonylation of alpha-allenic alcohols catalyzed by palladium chloride.

Wei Li1, Min Shi.   

Abstract

Vinylidenecyclopropanes undergo hydrobromination or alkoxybromination in the presence of N-bromosuccinimide and water or alcohols to give the corresponding vinylbromohydrin and vinylbromoalkoxy derivatives in moderate to excellent yields at room temperature. These vinylbromohydrin derivatives can be easily transformed to alpha-allenic alcohols in the presence of Et3N under mild conditions. In addition, the cyclocarbonylation of alpha-allenic alcohols with CO catalyzed by palladium chloride to give the corresponding lactones under different reaction conditions has been described.

Entities:  

Year:  2008        PMID: 18671429     DOI: 10.1021/jo8009352

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


  2 in total

1.  Highly stereoselective synthesis of (Z)- and (E)-chloro-substituted-α-methylene-γ-butyrolactone by possibly controlling cis- and trans-chloropalladation.

Authors:  Yi Dong; Xiaoyong Guo; Yuanyuan Yu; Gang Liu
Journal:  Mol Divers       Date:  2013-01-10       Impact factor: 2.943

2.  Diversification reactions of γ-silyl allenyl esters: selective conversion to all-carbon quaternary centers and γ-allene dicarbinols.

Authors:  Susovan Jana; Animesh Roy; Salvatore D Lepore
Journal:  Chem Commun (Camb)       Date:  2017-05-04       Impact factor: 6.222

  2 in total

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