Abstract
A series of chiral N-alkyl-1,2-diphenylaminoethanol/titanium/water complexes were investigated as potential efficient catalyst for the enantioselective oxidation of alkyl aryl sulfides. The structure of the aminoethanols strongly influenced on the reactivity and enantioselectivity. Using (1S,2S)-N-methyl-1,2-diphenylaminoethanol (6) as ligand in oxidation of methyl phenyl sulfide, gave (S)-sulfoxide with moderate yield and ee.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
