136764-66-4Relevant academic research and scientific papers
Facile stereoselective synthesis of cis- and trans-3-alkoxyazetidin-2-ones
Bhalla, Aman,Venugopalan, Paloth,Bari, Shamsher S.
, p. 8291 - 8302 (2007/10/03)
A highly stereoselective synthesis of cis- and trans-3-alkoxy-3-phenyl/benzylthioazetidin-2-ones is described. The reaction of α-chlorosulfide-β-lactams with various alcohols catalyzed by a Lewis acid such as ZnCl2 in the presence of molecular
Fluoride Ion Promoted Anodic Substitutions of Chalcogeno Compounds. 1. Regioselective Anodic Alkoxylation of Sulfides
Fuchigami, Toshio,Yano, Hidetoshi,Konno, Akinori
, p. 6731 - 6733 (2007/10/02)
Anodic α-alkoxylation of sulfides was remarkably promoted in the presence of fluoride ions: When Et3N*3HF was used as a supporting electrolyte, simple alkyl phenyl sulfides and sulfides bearing weak electron-withdrawing groups underwent anodic alkoxylatio
