Rapid Construction of a Chloromethyl-Substituted Duocarmycin-like Prodrug.

1,2,3,6-tetrahydropyrrolo[3,2-e]indole duocarmycin prodrug selective halogenation

Journal

Molecules (Basel, Switzerland)
ISSN: 1420-3049
Titre abrégé: Molecules
Pays: Switzerland
ID NLM: 100964009

Informations de publication

Date de publication:
16 Jun 2023
Historique:
received: 25 05 2023
revised: 15 06 2023
accepted: 15 06 2023
medline: 29 6 2023
pubmed: 28 6 2023
entrez: 28 6 2023
Statut: epublish

Résumé

The construction of duocarmycin-like compounds is often associated with lengthy synthetic routes. Presented herein is the development of a short and convenient synthesis of a type of duocarmycin prodrug. The 1,2,3,6-tetrahydropyrrolo[3,2-

Identifiants

pubmed: 37375372
pii: molecules28124818
doi: 10.3390/molecules28124818
pmc: PMC10304315
pii:
doi:

Substances chimiques

Duocarmycins 0
Prodrugs 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Références

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Auteurs

Christoffer Bengtsson (C)

Drug Discovery & Development Platform, Science for Life Laboratory, Department of Organic Chemistry, Stockholm University, Tomtebodavägen 23a, 17165 Solna, Sweden.

Ylva Gravenfors (Y)

Drug Discovery & Development Platform, Science for Life Laboratory, Department of Organic Chemistry, Stockholm University, Tomtebodavägen 23a, 17165 Solna, Sweden.

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Classifications MeSH