The Letter reports a safe and reliable synthesis of aryl 1,2,3-triazoles from the corresponding anilines via intermediate aryl azides, using a continuous process. The method was applied to a variety of substrates with good to excellent yields, without the need to isolate the reactive and possibly unstable intermediates which were constantly kept at low concentration in the matrix environment.

Highly efficient and safe procedure for the synthesis of aryl 1,2,3-triazoles from aromatic amine in a continuous flow reactor / F. Stazi, D. Cancogni, L. Turco, P. Westerduin, S. Bacchi. - In: TETRAHEDRON LETTERS. - ISSN 0040-4039. - 51:41(2010 Aug 01), pp. 5385-5387.

Highly efficient and safe procedure for the synthesis of aryl 1,2,3-triazoles from aromatic amine in a continuous flow reactor

D. Cancogni
Secondo
;
S. Bacchi
2010

Abstract

The Letter reports a safe and reliable synthesis of aryl 1,2,3-triazoles from the corresponding anilines via intermediate aryl azides, using a continuous process. The method was applied to a variety of substrates with good to excellent yields, without the need to isolate the reactive and possibly unstable intermediates which were constantly kept at low concentration in the matrix environment.
1,3-Cycloaddition; Aryl 1,2,3-triazoles; Flow chemistry; Organic azides; Biochemistry; Organic Chemistry; Drug Discovery3003 Pharmaceutical Science
Settore CHIM/06 - Chimica Organica
1-ago-2010
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/247623
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