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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Main Authors: Nakin Surapanich, Patcharin Chaisuwan, Chutima Kuhakarn, Vichai Reutrakul
Other Authors: Rajabhat Rajanagarindra University
Format: Review
Published: 2018
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/43377
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spelling 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
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Chemistry
spellingShingle 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
description © 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.
author2 Rajabhat Rajanagarindra University
author_facet Rajabhat Rajanagarindra University
Nakin Surapanich
Patcharin Chaisuwan
Chutima Kuhakarn
Vichai Reutrakul
format Review
author Nakin Surapanich
Patcharin Chaisuwan
Chutima Kuhakarn
Vichai Reutrakul
author_sort 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
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/43377
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