The Experts below are selected from a list of 324 Experts worldwide ranked by ideXlab platform
Yue Wang - One of the best experts on this subject based on the ideXlab platform.
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direct construction of 2 3 unsubstituted Benzofurans and benzothiophenes via a metal free catalyzed intramolecular friedel crafts reaction
Organic chemistry frontiers, 2019Co-Authors: Jiawei Huang, Shulin Meng, Xianyu Huang, Zhengwei Yang, Ting Qi, Chao Li, Yue Wang, Baolin LiAbstract:A highly effective and straightforward method for the construction of 2,3-unsubstituted Benzofurans and benzothiophenes by the intramolecular Friedel–Crafts reaction has been developed. This phosphoric acid-catalyzed method exhibits good functional group tolerance for both electron-withdrawing groups and electron-donating groups. We have successfully obtained benzofuran and benzothiophene derivatives with various substituents, and the yield was up to 94%. The development of this reaction provides a simple and efficient strategy for the construction of benzofuran and benzothiophene skeleton compounds.
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Direct construction of 2,3-unsubstituted Benzofurans and benzothiophenes via a metal-free catalyzed intramolecular Friedel–Crafts reaction
Organic Chemistry Frontiers, 2019Co-Authors: Jiawei Huang, Shulin Meng, Xianyu Huang, Zhengwei Yang, Yue WangAbstract:A highly effective and straightforward method for the construction of 2,3-unsubstituted Benzofurans and benzothiophenes by the intramolecular Friedel–Crafts reaction has been developed. This phosphoric acid-catalyzed method exhibits good functional group tolerance for both electron-withdrawing groups and electron-donating groups. We have successfully obtained benzofuran and benzothiophene derivatives with various substituents, and the yield was up to 94%. The development of this reaction provides a simple and efficient strategy for the construction of benzofuran and benzothiophene skeleton compounds.
Jiawei Huang - One of the best experts on this subject based on the ideXlab platform.
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direct construction of 2 3 unsubstituted Benzofurans and benzothiophenes via a metal free catalyzed intramolecular friedel crafts reaction
Organic chemistry frontiers, 2019Co-Authors: Jiawei Huang, Shulin Meng, Xianyu Huang, Zhengwei Yang, Ting Qi, Chao Li, Yue Wang, Baolin LiAbstract:A highly effective and straightforward method for the construction of 2,3-unsubstituted Benzofurans and benzothiophenes by the intramolecular Friedel–Crafts reaction has been developed. This phosphoric acid-catalyzed method exhibits good functional group tolerance for both electron-withdrawing groups and electron-donating groups. We have successfully obtained benzofuran and benzothiophene derivatives with various substituents, and the yield was up to 94%. The development of this reaction provides a simple and efficient strategy for the construction of benzofuran and benzothiophene skeleton compounds.
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Direct construction of 2,3-unsubstituted Benzofurans and benzothiophenes via a metal-free catalyzed intramolecular Friedel–Crafts reaction
Organic Chemistry Frontiers, 2019Co-Authors: Jiawei Huang, Shulin Meng, Xianyu Huang, Zhengwei Yang, Yue WangAbstract:A highly effective and straightforward method for the construction of 2,3-unsubstituted Benzofurans and benzothiophenes by the intramolecular Friedel–Crafts reaction has been developed. This phosphoric acid-catalyzed method exhibits good functional group tolerance for both electron-withdrawing groups and electron-donating groups. We have successfully obtained benzofuran and benzothiophene derivatives with various substituents, and the yield was up to 94%. The development of this reaction provides a simple and efficient strategy for the construction of benzofuran and benzothiophene skeleton compounds.
Baolin Li - One of the best experts on this subject based on the ideXlab platform.
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direct construction of 2 3 unsubstituted Benzofurans and benzothiophenes via a metal free catalyzed intramolecular friedel crafts reaction
Organic chemistry frontiers, 2019Co-Authors: Jiawei Huang, Shulin Meng, Xianyu Huang, Zhengwei Yang, Ting Qi, Chao Li, Yue Wang, Baolin LiAbstract:A highly effective and straightforward method for the construction of 2,3-unsubstituted Benzofurans and benzothiophenes by the intramolecular Friedel–Crafts reaction has been developed. This phosphoric acid-catalyzed method exhibits good functional group tolerance for both electron-withdrawing groups and electron-donating groups. We have successfully obtained benzofuran and benzothiophene derivatives with various substituents, and the yield was up to 94%. The development of this reaction provides a simple and efficient strategy for the construction of benzofuran and benzothiophene skeleton compounds.
Xianyu Huang - One of the best experts on this subject based on the ideXlab platform.
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direct construction of 2 3 unsubstituted Benzofurans and benzothiophenes via a metal free catalyzed intramolecular friedel crafts reaction
Organic chemistry frontiers, 2019Co-Authors: Jiawei Huang, Shulin Meng, Xianyu Huang, Zhengwei Yang, Ting Qi, Chao Li, Yue Wang, Baolin LiAbstract:A highly effective and straightforward method for the construction of 2,3-unsubstituted Benzofurans and benzothiophenes by the intramolecular Friedel–Crafts reaction has been developed. This phosphoric acid-catalyzed method exhibits good functional group tolerance for both electron-withdrawing groups and electron-donating groups. We have successfully obtained benzofuran and benzothiophene derivatives with various substituents, and the yield was up to 94%. The development of this reaction provides a simple and efficient strategy for the construction of benzofuran and benzothiophene skeleton compounds.
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Direct construction of 2,3-unsubstituted Benzofurans and benzothiophenes via a metal-free catalyzed intramolecular Friedel–Crafts reaction
Organic Chemistry Frontiers, 2019Co-Authors: Jiawei Huang, Shulin Meng, Xianyu Huang, Zhengwei Yang, Yue WangAbstract:A highly effective and straightforward method for the construction of 2,3-unsubstituted Benzofurans and benzothiophenes by the intramolecular Friedel–Crafts reaction has been developed. This phosphoric acid-catalyzed method exhibits good functional group tolerance for both electron-withdrawing groups and electron-donating groups. We have successfully obtained benzofuran and benzothiophene derivatives with various substituents, and the yield was up to 94%. The development of this reaction provides a simple and efficient strategy for the construction of benzofuran and benzothiophene skeleton compounds.
Shulin Meng - One of the best experts on this subject based on the ideXlab platform.
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direct construction of 2 3 unsubstituted Benzofurans and benzothiophenes via a metal free catalyzed intramolecular friedel crafts reaction
Organic chemistry frontiers, 2019Co-Authors: Jiawei Huang, Shulin Meng, Xianyu Huang, Zhengwei Yang, Ting Qi, Chao Li, Yue Wang, Baolin LiAbstract:A highly effective and straightforward method for the construction of 2,3-unsubstituted Benzofurans and benzothiophenes by the intramolecular Friedel–Crafts reaction has been developed. This phosphoric acid-catalyzed method exhibits good functional group tolerance for both electron-withdrawing groups and electron-donating groups. We have successfully obtained benzofuran and benzothiophene derivatives with various substituents, and the yield was up to 94%. The development of this reaction provides a simple and efficient strategy for the construction of benzofuran and benzothiophene skeleton compounds.
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Direct construction of 2,3-unsubstituted Benzofurans and benzothiophenes via a metal-free catalyzed intramolecular Friedel–Crafts reaction
Organic Chemistry Frontiers, 2019Co-Authors: Jiawei Huang, Shulin Meng, Xianyu Huang, Zhengwei Yang, Yue WangAbstract:A highly effective and straightforward method for the construction of 2,3-unsubstituted Benzofurans and benzothiophenes by the intramolecular Friedel–Crafts reaction has been developed. This phosphoric acid-catalyzed method exhibits good functional group tolerance for both electron-withdrawing groups and electron-donating groups. We have successfully obtained benzofuran and benzothiophene derivatives with various substituents, and the yield was up to 94%. The development of this reaction provides a simple and efficient strategy for the construction of benzofuran and benzothiophene skeleton compounds.
