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Katritzky AR, Rogovoy B, Klein C, et al. N-functionalized benzotriazole-1-carboximidoyl chlorides: synthetic equivalents for isocyanide dichlorides. J Org Chem. 2001;66(8):2854-7doi: 10.1021/jo001685o.
Katritzky, A. R., Rogovoy, B., Klein, C., Insuasty, H., Vvedensky, V., & Insuasty, B. (2001). N-functionalized benzotriazole-1-carboximidoyl chlorides: synthetic equivalents for isocyanide dichlorides. The Journal of organic chemistry, 66(8), 2854-7. https://doi.org/10.1021/jo001685o
Katritzky, A R, et al. "N-functionalized benzotriazole-1-carboximidoyl chlorides: synthetic equivalents for isocyanide dichlorides." The Journal of organic chemistry vol. 66,8 (2001): 2854-7. doi: https://doi.org/10.1021/jo001685o
Katritzky AR, Rogovoy B, Klein C, Insuasty H, Vvedensky V, Insuasty B. N-functionalized benzotriazole-1-carboximidoyl chlorides: synthetic equivalents for isocyanide dichlorides. J Org Chem. 2001 Apr 20;66(8):2854-7. doi: 10.1021/jo001685o. PMID: 11304212.
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J Org Chem. 2001 Apr 20;66(8):2854-7. doi: 10.1021/jo001685o.

N-functionalized benzotriazole-1-carboximidoyl chlorides: synthetic equivalents for isocyanide dichlorides.

The Journal of organic chemistry

A R Katritzky, B Rogovoy, C Klein, H Insuasty, V Vvedensky, B Insuasty

Affiliations

  1. Center for Heterocyclic Compounds, Department of Chemistry, University of Florida, Gainesville, FL 32611-7200, USA. [email protected]

PMID: 11304212 DOI: 10.1021/jo001685o

Abstract

Readily prepared N-functionalized benzotriazole-1-carboximidoyl chlorides are proposed as stable and novel isocyanide dichloride synthetic equivalents. Subsequent condensations of these new intermediates afford polysubstituted guanidines, S-aryl isothioureas, and 2-aminoquinazolin-4-thiones.

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