Vicinal dianions of diethyl α-aroylsuccinates: Preparation of functionalized-2,3-dihydrofurans and -furans, and diaxial 2,4-diaryl-3,7-dioxabicyclo[3.3.0]octanes
Vicinal dianions of diethyl α-aroylsuccinates react with aromatic aldehydes to provide functionalized 2,3-dihydrofurans as the major products together with γ-butyrolactones after treatment of the adducts obtained with a catalytic amount of p-toluenesulfonic acid in refluxing toluene. cis-2,3-Dihydro...
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th-mahidol.206852018-07-24T10:29:03Z Vicinal dianions of diethyl α-aroylsuccinates: Preparation of functionalized-2,3-dihydrofurans and -furans, and diaxial 2,4-diaryl-3,7-dioxabicyclo[3.3.0]octanes Manat Pohmakotr Arisara Issaree Laddawan Sampaongoen Patoomratana Tuchinda Vichai Reutrakul Mahidol University Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics Vicinal dianions of diethyl α-aroylsuccinates react with aromatic aldehydes to provide functionalized 2,3-dihydrofurans as the major products together with γ-butyrolactones after treatment of the adducts obtained with a catalytic amount of p-toluenesulfonic acid in refluxing toluene. cis-2,3-Dihydrofurans are used as precursors for the preparation of tetrasubstituted furans and diaxial 2,4-diaryl-3,7-dioxabicyclo[3.3.0]octanes. © 2003 Published by Elsevier Ltd. 2018-07-24T03:18:46Z 2018-07-24T03:18:46Z 2003-10-20 Article Tetrahedron Letters. Vol.44, No.43 (2003), 7937-7940 10.1016/j.tetlet.2003.09.005 00404039 2-s2.0-0141708670 https://repository.li.mahidol.ac.th/handle/123456789/20685 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0141708670&origin=inward |
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Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics Manat Pohmakotr Arisara Issaree Laddawan Sampaongoen Patoomratana Tuchinda Vichai Reutrakul Vicinal dianions of diethyl α-aroylsuccinates: Preparation of functionalized-2,3-dihydrofurans and -furans, and diaxial 2,4-diaryl-3,7-dioxabicyclo[3.3.0]octanes |
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Vicinal dianions of diethyl α-aroylsuccinates react with aromatic aldehydes to provide functionalized 2,3-dihydrofurans as the major products together with γ-butyrolactones after treatment of the adducts obtained with a catalytic amount of p-toluenesulfonic acid in refluxing toluene. cis-2,3-Dihydrofurans are used as precursors for the preparation of tetrasubstituted furans and diaxial 2,4-diaryl-3,7-dioxabicyclo[3.3.0]octanes. © 2003 Published by Elsevier Ltd. |
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Mahidol University |
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Mahidol University Manat Pohmakotr Arisara Issaree Laddawan Sampaongoen Patoomratana Tuchinda Vichai Reutrakul |
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Manat Pohmakotr Arisara Issaree Laddawan Sampaongoen Patoomratana Tuchinda Vichai Reutrakul |
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Manat Pohmakotr |
title |
Vicinal dianions of diethyl α-aroylsuccinates: Preparation of functionalized-2,3-dihydrofurans and -furans, and diaxial 2,4-diaryl-3,7-dioxabicyclo[3.3.0]octanes |
title_short |
Vicinal dianions of diethyl α-aroylsuccinates: Preparation of functionalized-2,3-dihydrofurans and -furans, and diaxial 2,4-diaryl-3,7-dioxabicyclo[3.3.0]octanes |
title_full |
Vicinal dianions of diethyl α-aroylsuccinates: Preparation of functionalized-2,3-dihydrofurans and -furans, and diaxial 2,4-diaryl-3,7-dioxabicyclo[3.3.0]octanes |
title_fullStr |
Vicinal dianions of diethyl α-aroylsuccinates: Preparation of functionalized-2,3-dihydrofurans and -furans, and diaxial 2,4-diaryl-3,7-dioxabicyclo[3.3.0]octanes |
title_full_unstemmed |
Vicinal dianions of diethyl α-aroylsuccinates: Preparation of functionalized-2,3-dihydrofurans and -furans, and diaxial 2,4-diaryl-3,7-dioxabicyclo[3.3.0]octanes |
title_sort |
vicinal dianions of diethyl α-aroylsuccinates: preparation of functionalized-2,3-dihydrofurans and -furans, and diaxial 2,4-diaryl-3,7-dioxabicyclo[3.3.0]octanes |
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2018 |
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https://repository.li.mahidol.ac.th/handle/123456789/20685 |
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1763494404309385216 |