25205-93-0Relevant articles and documents
Mercury(II) p-toluenesulfonate mediated synthesis of oxazoles under microwave irradiation
Lee, Jong Chan,Song, In-Goul
, p. 5891 - 5894 (2000)
Direct transformation of aromatic ketones into oxazoles in the presence of mercury(II) p-toluenesulfonate under microwave irradiation is described. (C) 2000 Elsevier Science Ltd.
[3 + 2] Cycloaddition/Oxidative Aromatization Sequence via Photoredox Catalysis: One-Pot Synthesis of Oxazoles from 2H-Azirines and Aldehydes
Zeng, Ting-Ting,Xuan, Jun,Ding, Wei,Wang, Kuan,Lu, Liang-Qiu,Xiao, Wen-Jing
supporting information, p. 4070 - 4073 (2015/09/01)
A novel [3 + 2] cycloaddition/oxidative aromatization sequence via visible light-induced photoredox catalysis is disclosed. It provides a general synthetic route to 2,4,5-trisubstituted oxazoles from easily accessible 2H-azirines and aldehydes under mild reaction conditions. The potential of this strategy was further demonstrated by the rapid synthesis of a cyclooxygenase-2 inhibitor as well as the success of employing electron-deficient alkenes and imines as the reaction partners.