Literature DB >> 21142089

Tin mediated allylation reactions of enol ethers in water.

Mei-Huey Lin1, Shiang-Fu Hung, Long-Zhi Lin, Wen-Shing Tsai, Tsung-Hsun Chuang.   

Abstract

Under tin-mediated Barbier-type reaction conditions, hydration of enol ethers takes place to form aldehydes that undergo allylation reactions. By using this process, various homoallylic alcohols and 2-halohomoallylic alcohols are produced in good to excellent yields.

Entities:  

Year:  2010        PMID: 21142089     DOI: 10.1021/ol102825t

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


  2 in total

1.  Triphosgene-amine base promoted chlorination of unactivated aliphatic alcohols.

Authors:  Andrés Villalpando; Caitlan E Ayala; Christopher B Watson; Rendy Kartika
Journal:  J Org Chem       Date:  2013-03-29       Impact factor: 4.354

2.  SnCl2/TiCl3-mediated deoximation of oximes in an aqueous solvent.

Authors:  Mei-Huey Lin; Han-Jun Liu; Cheng-Yu Chang; Wei-Cheng Lin; Tsung-Hsun Chuang
Journal:  Molecules       Date:  2012-03-01       Impact factor: 4.411

  2 in total

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