240805-44-1Relevant articles and documents
Visible-light-promoted oxidation/condensation of benzyl alcohols with dialkylacetamides to cinnamides
Yang, Tianlong,Lu, Maojian,Lin, Zhaowei,Huang, Mingqiang,Cai, Shunyou
supporting information, p. 449 - 453 (2019/01/24)
Oxidative cross-coupling reactions of benzyl alcohols with N,N-dialkylacetamides were developed only employing oxygen as the terminal oxidant, efficiently providing a new, novel protocol for the construction of multifunctionalized cinnamides with the synergistic effects of KOH, organic photocatalyst eosin Y, and visible light irradiation at room temperature. A broad substrate scope and mild reaction conditions are the prominent features of this transformation.
Highly diastereo- and enantioselective aziridination of α,β-unsaturated amides with diaziridine and mechanistic consideration on its stereochemistry
Ishihara, Hiroyuki,Hori, Kiyoto,Sugihara, Hiroyasu,Ito, Yoshio N.,Katsuki, Tsutomu
, p. 4272 - 4286 (2007/10/03)
During studies of aziridination of α,β-unsaturated amides with diaziridine, we found that we could prepare both the cis- and trans-aziridinecarboxamides by choosing an appropriately substituted diaziridine. While 3-monosubstituted diaziridine 2 was suitab
