Abstract
Abstract Chiral recognition of chiral amines 4–10 by lipophilic peptide derivatives 1–3 was studied spectrophotometrically in chloroform. Peptide 3 as compared with 2 indicated greater binding affinity and enantiomer selectivity towards the (R)-isomer of 4 and 6. Also 3 showed strikingly high binding and diastereoselectivity towards 9 and 10.
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.
