An efficient and convenient synthesis of chain lengthened homologs of the fungicide Metalaxyl

Article abstract of DOI:10.1080/00397919208021134

An efficient and convenient synthesis of chain lengthened homologs of the important fungicide Metalaxyl is described. The starting material utilized is 2,6-dimethylaniline and the sequence is accomplished utilizing Grignard reactions and ruthenium based o

Full text of DOI:10.1080/00397919208021134

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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An Efficient and Convenient
Synthesis of Chain Lengthened
Homologs of the Fungicide
Metalaxyl
John T. Gupton a , James G. Tarrant a , Richard H. Yu
a , Traci L. Solarz a & Hak-Fun Chow b
a Department of Chemistry , University of Central
Florida Orlando , Fl, 32816
b DowElanco, Letcombe Laboratory Letcombe Regis ,
Wantage England , OX129JT
Published online: 23 Sep 2006.
To cite this article: John T. Gupton , James G. Tarrant , Richard H. Yu , Traci L. Solarz
& Hak-Fun Chow (1992) An Efficient and Convenient Synthesis of Chain Lengthened
Homologs of the Fungicide Metalaxyl, Synthetic Communications: An International
Journal for Rapid Communication of Synthetic Organic Chemistry, 22:22, 3205-3214,
DOI: 10.1080/00397919208021134
To link to this article: http://dx.doi.org/10.1080/00397919208021134
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