In the context of our ongoing studies on chromane derivatives as inhibitors of the salicylate synthase from M. tuberculosis, we isolated a new, unexpected compound from the cyclization of 3-(propargyloxy)-5-benzyloxy-benzoic acid methyl ester. Its molecular structure was elucidated by means of 1D and 2D NMR analyses, FT-IR, ESI-MS, and HRMS.

Synthesis and Analytical Characterization of Cyclization Products of 3-Propargyloxy-5-benzyloxy-benzoic Acid Methyl Ester / M. Mori, G. Cazzaniga, D. Nava, E. Pini. - In: MOLBANK. - ISSN 1422-8599. - 2024:2(2024 Apr), pp. M1806.1-M1806.6. [10.3390/M1806]

Synthesis and Analytical Characterization of Cyclization Products of 3-Propargyloxy-5-benzyloxy-benzoic Acid Methyl Ester

M. Mori
Primo
Membro del Collaboration Group
;
G. Cazzaniga
Secondo
Membro del Collaboration Group
;
D. Nava
Penultimo
;
E. Pini
Ultimo
2024

Abstract

In the context of our ongoing studies on chromane derivatives as inhibitors of the salicylate synthase from M. tuberculosis, we isolated a new, unexpected compound from the cyclization of 3-(propargyloxy)-5-benzyloxy-benzoic acid methyl ester. Its molecular structure was elucidated by means of 1D and 2D NMR analyses, FT-IR, ESI-MS, and HRMS.
chromane derivatives; ring-closure; NMR spectroscopy; antitubercular agent
Settore CHIM/06 - Chimica Organica
apr-2024
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1046269
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