Abstract

Diastereomerically pure tridentate heteroorganic ligands containing hydroxyl, sulfinyl, and amino moieties as nucleophilic centers, capable of binding various organometallic reagents, have proven to be highly efficient catalysts in enantioselective aza-Henry reactions to give the desired products in very high yields (up to 98%) and with ees of up to 95%. The influence of the stereogenic centers, located on the sulfinyl sulfur atom and in the amino moiety on the stereochemical course of the reaction is also discussed.

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 call

Disclaimer: 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.