A Simple and Mild Microwave-Based Synthesis of Novel Functionalized Benzofulvenes
Abstract Benzofulvenes and their derivatives are useful molecular entities having applications as biologically active molecules, polymer precursors, and optoelectronic devices. We have developed a simple and mild synthetic method for the formulation of a variety of these interesting compounds. Using...
| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Georg Thieme Verlag KG
2018-07-01
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| Series: | SynOpen |
| Subjects: | |
| Online Access: | http://www.thieme-connect.de/DOI/DOI?10.1055/s-0037-1610366 |
| _version_ | 1811323445421539328 |
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| author | Adam C. Glass Katherine E. Caspary Cole Fisher Connor Whyte James Okubo Lev N. Zakharov |
| author_facet | Adam C. Glass Katherine E. Caspary Cole Fisher Connor Whyte James Okubo Lev N. Zakharov |
| author_sort | Adam C. Glass |
| collection | DOAJ |
| description | Abstract
Benzofulvenes and their derivatives are useful molecular entities having applications as biologically active molecules, polymer precursors, and optoelectronic devices. We have developed a simple and mild synthetic method for the formulation of a variety of these interesting compounds. Using carbonyl coupling techniques combined with microwave heating, a wide variety of functionalized benzofulvenes can be accessed rapidly in good yield. Furthermore, we have obtained five crystal structures further expanding a limited number of benzofulvene structures available. |
| first_indexed | 2024-04-13T13:54:14Z |
| format | Article |
| id | doaj.art-3bdfc6c9741e4d2da487614970bb26e2 |
| institution | Directory Open Access Journal |
| issn | 2509-9396 |
| language | English |
| last_indexed | 2024-04-13T13:54:14Z |
| publishDate | 2018-07-01 |
| publisher | Georg Thieme Verlag KG |
| record_format | Article |
| series | SynOpen |
| spelling | doaj.art-3bdfc6c9741e4d2da487614970bb26e22022-12-22T02:44:14ZengGeorg Thieme Verlag KGSynOpen2509-93962018-07-0102030256026210.1055/s-0037-1610366A Simple and Mild Microwave-Based Synthesis of Novel Functionalized BenzofulvenesAdam C. Glass0Katherine E. Caspary1Cole Fisher2Connor Whyte3James Okubo4Lev N. Zakharov5Department of Chemistry, Pacific Lutheran UniversityDepartment of Chemistry, Oregon State UniversityDepartment of Chemistry, Pacific Lutheran UniversityDepartment of Chemistry, Pacific Lutheran UniversityDepartment of Chemistry, Pacific Lutheran UniversityCAMCOR, University of OregonAbstract Benzofulvenes and their derivatives are useful molecular entities having applications as biologically active molecules, polymer precursors, and optoelectronic devices. We have developed a simple and mild synthetic method for the formulation of a variety of these interesting compounds. Using carbonyl coupling techniques combined with microwave heating, a wide variety of functionalized benzofulvenes can be accessed rapidly in good yield. Furthermore, we have obtained five crystal structures further expanding a limited number of benzofulvene structures available.http://www.thieme-connect.de/DOI/DOI?10.1055/s-0037-1610366aromaticitybenzofulvenesdbumicrowavemild |
| spellingShingle | Adam C. Glass Katherine E. Caspary Cole Fisher Connor Whyte James Okubo Lev N. Zakharov A Simple and Mild Microwave-Based Synthesis of Novel Functionalized Benzofulvenes SynOpen aromaticity benzofulvenes dbu microwave mild |
| title | A Simple and Mild Microwave-Based Synthesis of Novel Functionalized Benzofulvenes |
| title_full | A Simple and Mild Microwave-Based Synthesis of Novel Functionalized Benzofulvenes |
| title_fullStr | A Simple and Mild Microwave-Based Synthesis of Novel Functionalized Benzofulvenes |
| title_full_unstemmed | A Simple and Mild Microwave-Based Synthesis of Novel Functionalized Benzofulvenes |
| title_short | A Simple and Mild Microwave-Based Synthesis of Novel Functionalized Benzofulvenes |
| title_sort | simple and mild microwave based synthesis of novel functionalized benzofulvenes |
| topic | aromaticity benzofulvenes dbu microwave mild |
| url | http://www.thieme-connect.de/DOI/DOI?10.1055/s-0037-1610366 |
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