| Literature DB >> 31361494 |
Iris R Landman1, Emilio Acuña-Bolomey1, Rosario Scopelliti1, Farzaneh Fadaei-Tirani1, Kay Severin1.
Abstract
1-Acyl triazenes can be prepared by acid-catalyzed hydration, gold/iodine-catalyzed oxidation, or oxyhalogenation of 1-alkynyl triazenes. Crystallographic analyses reveal a pronounced effect of the acyl group on the electronic structure of the triazene function. 1-Acyl triazenes display high thermal stability, and only moderate sensitivity toward hydrolysis. They are compatible with basic and oxidative conditions, allowing subsequent transformation. Under acidic conditions, 1-acyl triazenes act as acylation reagents.Entities:
Year: 2019 PMID: 31361494 DOI: 10.1021/acs.orglett.9b02248
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005