| Molecules | |
| Synthesis of a 2,2'-Bipyridyl Functionalized Oligovinylene-Phenylene Using Heck and Horner-Wadsworth-Emmons Reactions and X-ray Crystal Structure of E-(4-(4-Bromostyryl)phenyl)(methyl)sulfane | |
| Orsolya Karácsony1  Jeffrey R. Deschamps1  Scott A. Trammell1  Rafaela Nita1  | |
| [1] 1Chemistry Department, Florida Institute of Technology, 150 West University Boulevard, Melbourne, FL 32901, USA 2Center for Bio/Molecular Science and Engineering, US Naval Research Laboratory, 4555 Overlook Avenue, SW, Washington, DC 20375, USA †Current address: Chemistry Department, Carnegie Mellon University, Pittsburgh, PA 15213, USA. | |
| 关键词: oligovinylphenylene; HWE reaction; Heck coupling; | |
| DOI : 10.3390/molecules17055724 | |
| 来源: mdpi | |
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【 摘 要 】
The synthesis of a new 2,2'-bipyridyl functionalized oligovinylenephenylene (OVP-5) containing a methyl protected thiol using Heck coupling and the Horner-Wadsworth-Emmons reaction and is described. A key step involving a diisopropylcarbodiimide promoted dehydration of a stable b-hydroxyphosphonate intermediate was identified. The structure of precursor E-(4-(4-bromostyryl)phenyl)(methyl)sulfane (1) was determined using X-ray crystallography.
【 授权许可】
CC BY
This is an open access article distributed under the Creative Commons Attribution License (CC BY) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| RO202003190044072ZK.pdf | 528KB |
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