68972-96-3Relevant articles and documents
Chemoenzymatic route to stereodefined 2-(azidophenyl)oxazolines for click chemistry
Monsen, Paige J.,Luzzio, Frederick A.
supporting information, (2020/12/29)
Aryl-substituted esters of a racemic diprotected 2-azido-1-alkanol were submitted to the Staudinger/aza-Wittig reaction in order to assess scope and establish conditions for their cyclization to the corresponding 2,4,5-trisubstituted oxazolines. Following
Copper-Catalyzed Oxyalkynylation of C-S Bonds in Thiiranes and Thiethanes with Hypervalent Iodine Reagents
Borrel, Julien,Pisella, Guillaume,Waser, Jerome
supporting information, p. 422 - 427 (2020/01/31)
We report the oxyalkynylation of thiiranes and thietanes using ethynylbenziodoxolone reagents (EBXs) to readily access functionalized building blocks bearing an alkynyl, a benzoate, and an iodide group. The reaction proceeds with high atom efficiency most
Fe2O3-Promoted Intermolecular Chlorotrifluoromethylthiolation of Alkenes
Jia, Yimin,Qin, Hongmei,Wang, Na,Jiang, Zhong-Xing,Yang, Zhigang
, p. 2808 - 2817 (2018/03/09)
A simple, convenient method for intermolecular chlorotrifluoromethylthiolation of alkenes by using a low-cost and more abundant iron catalyst has been developed. This protocol provides a straightforward way to synthesize a variety of useful SCF3/sub