Organopromoted Direct Synthesis of 1,1-Diphenyl-3-arylindanes via Formal [3+2] Cycloadditions of Triphenylcarbenium Tetrafluoroborate with Styrenes
© Georg Thieme Verlag Stuttgart.New York-Synlett 2016. A formal [3+2] cycloaddition of triphenylcarbenium tetrafluoroborate with structurally different styrene derivatives has been developed. A combination of benzophenone and Et3N is key for promoting a formal [3+2] cycloaddition of triphenylcarbeni...
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th-mahidol.433772019-03-14T15:04:26Z Organopromoted Direct Synthesis of 1,1-Diphenyl-3-arylindanes via Formal [3+2] Cycloadditions of Triphenylcarbenium Tetrafluoroborate with Styrenes Nakin Surapanich Patcharin Chaisuwan Chutima Kuhakarn Vichai Reutrakul Rajabhat Rajanagarindra University Suranaree University of Technology Mahidol University Chemistry © Georg Thieme Verlag Stuttgart.New York-Synlett 2016. A formal [3+2] cycloaddition of triphenylcarbenium tetrafluoroborate with structurally different styrene derivatives has been developed. A combination of benzophenone and Et3N is key for promoting a formal [3+2] cycloaddition of triphenylcarbenium tetrafluoroborate with styrenes affording 1,1-diphenyl-3-arylindanes in moderate to good yields. The reaction mechanism of this transformation is also discussed. 2018-12-11T02:31:45Z 2019-03-14T08:04:26Z 2018-12-11T02:31:45Z 2019-03-14T08:04:26Z 2016-12-01 Review Synlett. Vol.27, No.19 (2016), 2689-2694 10.1055/s-0036-1588302 14372096 09365214 2-s2.0-84984850896 https://repository.li.mahidol.ac.th/handle/123456789/43377 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84984850896&origin=inward |
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Chemistry Nakin Surapanich Patcharin Chaisuwan Chutima Kuhakarn Vichai Reutrakul Organopromoted Direct Synthesis of 1,1-Diphenyl-3-arylindanes via Formal [3+2] Cycloadditions of Triphenylcarbenium Tetrafluoroborate with Styrenes |
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© Georg Thieme Verlag Stuttgart.New York-Synlett 2016. A formal [3+2] cycloaddition of triphenylcarbenium tetrafluoroborate with structurally different styrene derivatives has been developed. A combination of benzophenone and Et3N is key for promoting a formal [3+2] cycloaddition of triphenylcarbenium tetrafluoroborate with styrenes affording 1,1-diphenyl-3-arylindanes in moderate to good yields. The reaction mechanism of this transformation is also discussed. |
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Rajabhat Rajanagarindra University |
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Rajabhat Rajanagarindra University Nakin Surapanich Patcharin Chaisuwan Chutima Kuhakarn Vichai Reutrakul |
format |
Review |
author |
Nakin Surapanich Patcharin Chaisuwan Chutima Kuhakarn Vichai Reutrakul |
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Nakin Surapanich |
title |
Organopromoted Direct Synthesis of 1,1-Diphenyl-3-arylindanes via Formal [3+2] Cycloadditions of Triphenylcarbenium Tetrafluoroborate with Styrenes |
title_short |
Organopromoted Direct Synthesis of 1,1-Diphenyl-3-arylindanes via Formal [3+2] Cycloadditions of Triphenylcarbenium Tetrafluoroborate with Styrenes |
title_full |
Organopromoted Direct Synthesis of 1,1-Diphenyl-3-arylindanes via Formal [3+2] Cycloadditions of Triphenylcarbenium Tetrafluoroborate with Styrenes |
title_fullStr |
Organopromoted Direct Synthesis of 1,1-Diphenyl-3-arylindanes via Formal [3+2] Cycloadditions of Triphenylcarbenium Tetrafluoroborate with Styrenes |
title_full_unstemmed |
Organopromoted Direct Synthesis of 1,1-Diphenyl-3-arylindanes via Formal [3+2] Cycloadditions of Triphenylcarbenium Tetrafluoroborate with Styrenes |
title_sort |
organopromoted direct synthesis of 1,1-diphenyl-3-arylindanes via formal [3+2] cycloadditions of triphenylcarbenium tetrafluoroborate with styrenes |
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2018 |
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https://repository.li.mahidol.ac.th/handle/123456789/43377 |
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1763490284856934400 |