Monoterpene Thiols: Synthesis and Modifications for Obtaining Biologically Active Substances.

antimicrobial activity asymmetric synthesis disulfides monoterpenoids sulfenimines sulfinamides thiols thiosulfonates

Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
01 Nov 2023
Historique:
received: 10 10 2023
revised: 26 10 2023
accepted: 30 10 2023
medline: 15 11 2023
pubmed: 14 11 2023
entrez: 14 11 2023
Statut: epublish

Résumé

Monoterpene thiols are one of the classes of natural flavors that impart the smell of citrus fruits, grape must and wine, black currants, and guava and are used as flavoring agents in the food and perfume industries. Synthetic monoterpene thiols have found an application in asymmetric synthesis as chiral auxiliaries, derivatizing agents, and ligands for metal complex catalysis and organocatalysts. Since monoterpenes and monoterpenoids are a renewable source, there are emerging trends to use monoterpene thiols as monomers for producing new types of green polymers. Monoterpene thioderivatives are also known to possess antioxidant, anticoagulant, antifungal, and antibacterial activity. The current review covers methods for the synthesis of acyclic, mono-, and bicyclic monoterpene thiols, as well as some investigations related to their usage for the preparation of the compounds with antimicrobial properties.

Identifiants

pubmed: 37958865
pii: ijms242115884
doi: 10.3390/ijms242115884
pmc: PMC10649346
pii:
doi:

Substances chimiques

Monoterpenes 0
Sulfhydryl Compounds 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Russian Science Foundation
ID : 21-13-00245

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Auteurs

Denis V Sudarikov (DV)

Institute of Chemistry, Federal Research Center "Komi Scientific Center", Ural Branch, Russian Academy of Sciences, 167000 Syktyvkar, Russia.

Liliya E Nikitina (LE)

General and Organic Chemistry Department, Kazan State Medical University, 49 Butlerov St., 420012 Kazan, Russia.

Patrick Rollin (P)

Institute of Organic and Analytical Chemistry (ICOA), Université d'Orléans et the French National Center for Scientific Research (CNRS), UMR 7311, BP 6759, F-45067 Orléans, France.

Evgeniy S Izmest'ev (ES)

Institute of Chemistry, Federal Research Center "Komi Scientific Center", Ural Branch, Russian Academy of Sciences, 167000 Syktyvkar, Russia.

Svetlana A Rubtsova (SA)

Institute of Chemistry, Federal Research Center "Komi Scientific Center", Ural Branch, Russian Academy of Sciences, 167000 Syktyvkar, Russia.

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Classifications MeSH