Pushing at the Boundaries of Pterin Chemistry.
Sonogashira cross-coupling
Suzuki cross-coupling
pterin
solid-state mechano-synthesis
tosylation
Journal
Molecules (Basel, Switzerland)
ISSN: 1420-3049
Titre abrégé: Molecules
Pays: Switzerland
ID NLM: 100964009
Informations de publication
Date de publication:
27 Sep 2024
27 Sep 2024
Historique:
received:
02
08
2024
revised:
23
09
2024
accepted:
24
09
2024
medline:
16
10
2024
pubmed:
16
10
2024
entrez:
16
10
2024
Statut:
epublish
Résumé
Pterins are molecules of substantial interest as they occur in nature in a number of forms with quite distinct and often indispensable roles. Chemically, the synthesis of the principle pterin scaffold is comparably simple, while the insolubility of the pterin building block renders synthetic derivatization extremely difficult. When aiming at modeling naturally occurring pterins of extended chemical structure, this is a considerable problem. A notable set of strategies was developed in the course of the present study, which are able to overcome the lack of reactivity of the pterin backbone. These include a strategic choice regarding protection groups, uncommon chemical transformation, ball milling and combinations thereof. Some novel pterins with quite distinct substitution motifs were successfully synthesized and characterized by spectroscopic and spectrometric analyses as well as single-crystal structural analyses for three of them.
Identifiants
pubmed: 39407518
pii: molecules29194587
doi: 10.3390/molecules29194587
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM