An improved total synthesis of tunicamycin V.

A practical synthesis of tunicamycin V Azidonitration Büchner-Curtius-Schlotterbeck reaction Practical synthesis Tunicamycins

Journal

MethodsX
ISSN: 2215-0161
Titre abrégé: MethodsX
Pays: Netherlands
ID NLM: 101639829

Informations de publication

Date de publication:
2023
Historique:
received: 30 11 2022
accepted: 22 02 2023
entrez: 13 3 2023
pubmed: 14 3 2023
medline: 14 3 2023
Statut: epublish

Résumé

The tunicamycins are important biochemical tools to study

Identifiants

pubmed: 36911209
doi: 10.1016/j.mex.2023.102095
pii: S2215-0161(23)00097-3
pmc: PMC9995453
doi:

Types de publication

Journal Article

Langues

eng

Pagination

102095

Informations de copyright

© 2023 The Author(s).

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Références

Angew Chem Int Ed Engl. 2015 May 26;54(22):6618-21
pubmed: 25873339
Org Lett. 2018 Jan 5;20(1):256-259
pubmed: 29256622
Angew Chem Int Ed Engl. 2022 Aug 1;61(31):e202203225
pubmed: 35594368

Auteurs

Katsuhiko Mitachi (K)

Department of Pharmaceutical Sciences, College of Pharmacy, University of Tennessee Health Science Center, 881 Madison Avenue, Memphis, TN 38163, USA.

David Mingle (D)

Department of Pharmaceutical Sciences, College of Pharmacy, University of Tennessee Health Science Center, 881 Madison Avenue, Memphis, TN 38163, USA.

Michio Kurosu (M)

Department of Pharmaceutical Sciences, College of Pharmacy, University of Tennessee Health Science Center, 881 Madison Avenue, Memphis, TN 38163, USA.

Classifications MeSH