Abstract
Enantiomerically pure α-alkyl-ω-aminocarboxylic acids 5, 6 and the corresponding α-alkyllactams 7 are synthesized starting from lactams 1 by ring transformation with a chiral aminoalcohol 2, asymmetric α-alkylation of the resulting 2-(ω-aminoalkyl)-oxazolines 3 and final hydrolysis.
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 callSimilar Papers
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.
