Primary α-Phosphino- and α-Arseno-Nitriles, Analogues of α-Aminonitriles.
Journal
Inorganic chemistry
ISSN: 1520-510X
Titre abrégé: Inorg Chem
Pays: United States
ID NLM: 0366543
Informations de publication
Date de publication:
31 May 2024
31 May 2024
Historique:
medline:
31
5
2024
pubmed:
31
5
2024
entrez:
31
5
2024
Statut:
aheadofprint
Résumé
More than 170 years after the synthesis of α-aminonitriles by the reaction of Strecker, α-phosphinonitriles, and α-arsenonitriles have been prepared and characterized by NMR and IR spectroscopy. For the simplest derivatives, the reaction was carried out by reaction of cyanomethyltributylstannane with phosphorus or arsenic trichloride, followed by a chemoselective reduction of the dichlorophosphine and dichloroarsine formed to the corresponding primary phosphine and arsine. The phosphinoacetonitrile can be stored at -80 °C for months in its pure state, but arsenoacetonitrile decomposes at this temperature. Chiral compounds can be synthesized from C-substituted cyano-1-alkyltributylstannanes. In
Identifiants
pubmed: 38818931
doi: 10.1021/acs.inorgchem.4c01307
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM