Synthesis of acylamido ketene dithioacetals and 5-oxo-4,5-dihydrobenzo[f]-1,4-thiazepine-derivatives by dithiocarboxylation of α-aza-c-nucleophiles

Article abstract of DOI:10.1080/10426509708043496

N-acceptor methyl substituted 2,2,N-trimethyl-propionamides (1 acc-group = p-MeOC₆H₄CO-, 2 acc-group = COOMe) afford in the procedure of dithiocarboxylation 3,3-[bis(alkylthio)]-prop-2-ene-1-ones 4a-c and methyl 3,3-[bis(alkylthio)]-

Full text of DOI:10.1080/10426509708043496

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Phosphorus, Sulfur, and Silicon and
the Related Elements
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SYNTHESIS OF ACYLAMIDO
KETENE DITHIOACETALS AND 5-
OXO-4,5-DIHYDROBENZO[F]-1,4-
THIAZEPINE-DERIVATIVES BY
DITHIOCARBOXYLATION OF α-AZA-C-
NUCLEOPHILES
Wolfgang Dölling a
a Martin-Luther University Halle-Wittenberg, Department
of Chemistry, Institute of Organic Chemistry , Kurt-Mothes-
Straße 2, D-06120, Halle (Saale), Germany
Published online: 04 Oct 2006.
To cite this article: Wolfgang Dölling (1997) SYNTHESIS OF ACYLAMIDO KETENE
DITHIOACETALS AND 5-OXO-4,5-DIHYDROBENZO[F]-1,4-THIAZEPINE-DERIVATIVES BY
DITHIOCARBOXYLATION OF α-AZA-C-NUCLEOPHILES, Phosphorus, Sulfur, and Silicon and the
Related Elements, 122:1, 71-86, DOI: 10.1080/10426509708043496
To link to this article: http://dx.doi.org/10.1080/10426509708043496
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