A new route to dithiocarbamates from tertiary N-methyl and N-benzylamines

Article abstract of DOI:10.1080/00397919208019304

The sequential treatment of various tertiary N-methyl and N-benzylamines with carbon disulfide, and then with an alkyl halide in tetrahydrofuran gave the corresponding dithiocarbamates in good to excellent yields.

Full text of DOI:10.1080/00397919208019304

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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A New Route to
Dithiocarbamates from Tertiary
N-Methyl and N-Benzylamines
M. D. Pujol a & G. Guillaumet a
a Laboratoire de Chimie Bioorganique et Analytique
associé au CNRS (URA 499), Université d′Orléans, BP
6759, 45067, Orléans Cedex 2, France
Version of record first published: 24 Sep 2006
To cite this article: M. D. Pujol & G. Guillaumet (1992): A New Route to
Dithiocarbamates from Tertiary N-Methyl and N-Benzylamines, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 22:9, 1231-1238
To link to this article: http://dx.doi.org/10.1080/00397919208019304
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