Literature DB >> 11700128

An efficient combination of microwave dielectric heating and the use of solid-supported triphenylphosphine for Wittig reactions.

J Westman1.   

Abstract

[reaction--see text] Olefins could be formed in an efficient way by the use of stable ylides in just a few minutes using microwave dielectric heating. The drawback with the Wittig reaction in solution phase is the formation of 1 equiv of triphenylphosphine oxide. To avoid this, the corresponding protocol using the efficient combination of solid-supported triphenylphosphine and microwave dielectric heating was developed. An even more efficient one-pot three-step Wittig reaction was also developed.

Entities:  

Year:  2001        PMID: 11700128     DOI: 10.1021/ol0167053

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


  6 in total

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5.  Bridged [2.2.1] bicyclic phosphine oxide facilitates catalytic γ-umpolung addition-Wittig olefination.

Authors:  Kui Zhang; Lingchao Cai; Zhongyue Yang; K N Houk; Ohyun Kwon
Journal:  Chem Sci       Date:  2018-01-18       Impact factor: 9.825

6.  Microwave-Assisted Expeditious Synthesis of 2-Alkyl-2-(N-arylsulfonylindol-3-yl)-3-N-acyl-5-aryl-1,3,4-oxadiazolines Catalyzed by HgCl₂ under Solvent-Free Conditions as Potential Anti-HIV-1 Agents.

Authors:  Zhiping Che; Yuee Tian; Shengming Liu; Jia Jiang; Mei Hu; Genqiang Chen
Journal:  Molecules       Date:  2018-11-10       Impact factor: 4.411

  6 in total

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