Synthesis and mercury (II) trifluoroacetate mediated cyclization of N- aryl N-allenylmethyl carbamide

Article abstract of DOI:10.1080/00397919408010171

A three step sequence is described for conversion of substituted phenyl carbamide into 1-cyano-4-methylidene-1,2,3,4-tetrahydro quinoline involving N-propargylation, allene formation followed by mercury (II) trifluoro acetate catalysed cyclization.

Full text of DOI:10.1080/00397919408010171

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Synthetic Communications: An
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Synthesis and Mercury (II)
Trifluoroacetate Mediated
Cyclization of N-Aryl -
Allenylmethyl Carbamide
B. Devan a & K. Rajagopalan a
a Department of Organic Chemistry , University of
Madras , Guindy Campus, Madras, 600 025, INDIA
Published online: 23 Sep 2006.
To cite this article: B. Devan & K. Rajagopalan (1994) Synthesis and Mercury (II)
Trifluoroacetate Mediated Cyclization of N-Aryl -Allenylmethyl Carbamide, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 24:12, 1691-1700, DOI: 10.1080/00397919408010171
To link to this article: http://dx.doi.org/10.1080/00397919408010171
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