Abstract
A novel one-pot synthesis was developed for the preparation of partial amide esters of (dichloromethylene)bisphosphonic acid from readily available tetramethyl ester with good selectivity and purity.
Keywords: Bisphosphonate, amide esters, selective synthesis, mesyl leaving group, amination
Letters in Organic Chemistry
Title: Novel One-Pot Synthesis of Amide Derivatives of Methylenebisphosphonate Utilizing the Mesyl Moiety as Leaving Group
Volume: 3 Issue: 12
Author(s): Jonna Jokiniemi, Markku Ahlgren and Jouko J. Vepsalainen
Affiliation:
Keywords: Bisphosphonate, amide esters, selective synthesis, mesyl leaving group, amination
Abstract: A novel one-pot synthesis was developed for the preparation of partial amide esters of (dichloromethylene)bisphosphonic acid from readily available tetramethyl ester with good selectivity and purity.
Export Options
About this article
Cite this article as:
Jokiniemi Jonna, Ahlgren Markku and Vepsalainen J. Jouko, Novel One-Pot Synthesis of Amide Derivatives of Methylenebisphosphonate Utilizing the Mesyl Moiety as Leaving Group, Letters in Organic Chemistry 2006; 3 (12) . https://dx.doi.org/10.2174/157017806779467951
DOI https://dx.doi.org/10.2174/157017806779467951 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
- Author Guidelines
- Graphical Abstracts
- Fabricating and Stating False Information
- Research Misconduct
- Post Publication Discussions and Corrections
- Publishing Ethics and Rectitude
- Increase Visibility of Your Article
- Archiving Policies
- Peer Review Workflow
- Order Your Article Before Print
- Promote Your Article
- Manuscript Transfer Facility
- Editorial Policies
- Allegations from Whistleblowers