The reactivity of safracin B is investigated as a platform for the efficient synthesis of cyanosafracin B and safracin A, with particular emphasis on the optimization of reaction conditions to achieve high yield and purity. In addition, a complete assignment of the nuclear magnetic resonance spectra of these structurally complex members of the safracin family is reported. Overall, this study deepens the understanding of structure–reactivity relationships within safracin natural products and highlights their value as versatile scaffolds for synthetic, analytical, and medicinal chemistry applications.

Safracin B as a Synthetic Linchpin: From Natural Product to Drug Intermediate and Beyond / P. Orlando, S.B.. - In: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY. - ISSN 1099-0690. - (2026), pp. e70616.1-e70616.6. [Epub ahead of print] [10.1002/ejoc.70616]

Safracin B as a Synthetic Linchpin: From Natural Product to Drug Intermediate and Beyond

P. Orlando
Co-primo
;
S. Borsoi
Co-primo
;
V. Fasano
Secondo
;
A. Citarella;D. Passarella
Ultimo
2026

Abstract

The reactivity of safracin B is investigated as a platform for the efficient synthesis of cyanosafracin B and safracin A, with particular emphasis on the optimization of reaction conditions to achieve high yield and purity. In addition, a complete assignment of the nuclear magnetic resonance spectra of these structurally complex members of the safracin family is reported. Overall, this study deepens the understanding of structure–reactivity relationships within safracin natural products and highlights their value as versatile scaffolds for synthetic, analytical, and medicinal chemistry applications.
cyanosafracin b; natural products chemistry; safracin b; trabectedin; α-amino nitriles;
Settore CHEM-05/A - Chimica organica
2026
9-giu-2026
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1257776
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