Year-end Sale % OFF 
Abstract
Under high concentration conditions, tripodal trialdehyde 1 undergoes [2+3] Schiff base condensation with linear aliphatic diamines at room temperature to form macrobicyclic cryptands while two tripodal trialdehydes 1 or 2 undergo [2+2] Schiff base condensation with two tripodal triamines to form macrotricylic cryptands. Another macrotricyclic cryptand is formed via [4+6] amidation reaction.
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.
