A one-pot, water compatible synthesis of pyrimidine nucleobases under plausible prebiotic conditions.


Journal

Chemical communications (Cambridge, England)
ISSN: 1364-548X
Titre abrégé: Chem Commun (Camb)
Pays: England
ID NLM: 9610838

Informations de publication

Date de publication:
07 Feb 2019
Historique:
pubmed: 27 1 2019
medline: 27 1 2019
entrez: 26 1 2019
Statut: ppublish

Résumé

Herein, we report a new prebiotically plausible pathway towards a pyrimidine nucleobase in continuous manner. The route involves simultaneous methylation and carbamoylation of cyanoacetylene-derived α,β-unsaturated thioamide with N-methyl-N-nitrosourea (MNU) in aqueous media. This provides S-methylpyrimidinone in one-pot, which can be converted into a variety of 4-substituted pyrimidine nucleobases including cytosine and uracil.

Identifiants

pubmed: 30681091
doi: 10.1039/c8cc09435g
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1939-1942

Auteurs

Hidenori Okamura (H)

Center for Integrated Protein Science (CiPSM) at the Department of Chemistry, Ludwig-Maximilians-Universität München, Butenandtstr. 5-13, 81377 München, Germany. thomas.carell@lmu.de.

Classifications MeSH