Abstract
A mild and improved synthesis of disecondary phosphines PhPH(CH2)nPHPh (where n = 1-6), have been prepared. In the presence of phenylphosphine, cesium hydroxide, activated 4 Å molecular sieves and DMF, numerous dialkyl halides reacted efficiently to produce various disecondary phosphines exclusively at room temperature.
Keywords: primary phosphine, cesium hydroxide monohydrate, dialkyl halide, disecondary phosphine, phosphine macrocycle
Letters in Organic Chemistry
Title: A Mild and Efficient Synthesis of Disecondary Phosphines Using CsOH: Efforts Toward Phosphine Macrocycles
Volume: 2 Issue: 2
Author(s): Matthew T. Honaker and Ralph N. Salvatore
Affiliation:
Keywords: primary phosphine, cesium hydroxide monohydrate, dialkyl halide, disecondary phosphine, phosphine macrocycle
Abstract: A mild and improved synthesis of disecondary phosphines PhPH(CH2)nPHPh (where n = 1-6), have been prepared. In the presence of phenylphosphine, cesium hydroxide, activated 4 Å molecular sieves and DMF, numerous dialkyl halides reacted efficiently to produce various disecondary phosphines exclusively at room temperature.
Export Options
About this article
Cite this article as:
Honaker T. Matthew and Salvatore N. Ralph, A Mild and Efficient Synthesis of Disecondary Phosphines Using CsOH: Efforts Toward Phosphine Macrocycles, Letters in Organic Chemistry 2005; 2 (2) . https://dx.doi.org/10.2174/1570178053202874
DOI https://dx.doi.org/10.2174/1570178053202874 |
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