Abstract
Phosphoramide derivatives 13 and 15 were prepared as analogues of sphinganine-1-phosphate ( 4). Key steps of the synthesis are the alkylation of N-methoxy-N-methlycarboxyamide of the diaminopropanoic acid 7 and the subsequent reduction of the intermediately formed ketone 8 affording the diastereomeric alcohols 9. Deprotection and phosphorylation of 9 lead to the desired products 13 and 15.
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 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.
