The Experts below are selected from a list of 312 Experts worldwide ranked by ideXlab platform
Bowen Fang - One of the best experts on this subject based on the ideXlab platform.
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pti2 catalyzed tandem 3 3 rearrangement nazarov reaction of arylpropargylic esters synthesis of Indanone derivatives
Organic and Biomolecular Chemistry, 2011Co-Authors: Huaiji Zheng, Juan Yang, Changgui Zhao, Peng Jing, Bowen FangAbstract:An efficient PtI2-catalyzed tandem reaction of arylpropargylic esters, involving 3,3-rearrangement and Nazarov reaction, has been developed to produce 3-substituted and 3,3-disubstituted Indanone derivatives. This approach provided a pathway to the synthesis of Indanone skeletons in natural products.
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PtI2-Catalyzed tandem 3,3-rearrangement/Nazarov reaction of arylpropargylic esters: synthesis of Indanone derivatives
Organic & biomolecular chemistry, 2011Co-Authors: Huaiji Zheng, Juan Yang, Changgui Zhao, Peng Jing, Bowen Fang, Xingang Xie, Xuegong SheAbstract:An efficient PtI2-catalyzed tandem reaction of arylpropargylic esters, involving 3,3-rearrangement and Nazarov reaction, has been developed to produce 3-substituted and 3,3-disubstituted Indanone derivatives. This approach provided a pathway to the synthesis of Indanone skeletons in natural products.
Huaiji Zheng - One of the best experts on this subject based on the ideXlab platform.
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pti2 catalyzed tandem 3 3 rearrangement nazarov reaction of arylpropargylic esters synthesis of Indanone derivatives
Organic and Biomolecular Chemistry, 2011Co-Authors: Huaiji Zheng, Juan Yang, Changgui Zhao, Peng Jing, Bowen FangAbstract:An efficient PtI2-catalyzed tandem reaction of arylpropargylic esters, involving 3,3-rearrangement and Nazarov reaction, has been developed to produce 3-substituted and 3,3-disubstituted Indanone derivatives. This approach provided a pathway to the synthesis of Indanone skeletons in natural products.
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PtI2-Catalyzed tandem 3,3-rearrangement/Nazarov reaction of arylpropargylic esters: synthesis of Indanone derivatives
Organic & biomolecular chemistry, 2011Co-Authors: Huaiji Zheng, Juan Yang, Changgui Zhao, Peng Jing, Bowen Fang, Xingang Xie, Xuegong SheAbstract:An efficient PtI2-catalyzed tandem reaction of arylpropargylic esters, involving 3,3-rearrangement and Nazarov reaction, has been developed to produce 3-substituted and 3,3-disubstituted Indanone derivatives. This approach provided a pathway to the synthesis of Indanone skeletons in natural products.
Zhen Yang - One of the best experts on this subject based on the ideXlab platform.
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A rhodium-catalyzed tandem reaction of N-sulfonyl triazoles with indoles: access to indole-substituted Indanones.
Chemical communications (Cambridge England), 2017Co-Authors: Hao Yuan, Jianxian Gong, Zhen YangAbstract:An efficient strategy for the synthesis of structurally diverse indole-substituted Indanones via a rhodium(ii)-catalyzed tandem reaction of N-sulfonyltriazoles with indoles was developed. The reaction involves rhodium(ii)-catalyzed denitrogenation of the N-sulfonyltriazoles to form an oxonium ylide, followed by nucleophilic addition of the indoles and subsequent skeletal rearrangement. This strategy provides straightforward access to Indanone frameworks bearing quaternary carbon centers.
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tunable and chemoselective syntheses of dihydroisobenzofurans and Indanones via rhodium catalyzed tandem reactions of 2 triazole benzaldehydes and 2 triazole alkylaryl ketones
Organic Letters, 2014Co-Authors: Hongjuan Shen, Jianxian Gong, Zhen YangAbstract:Two novel rhodium(II)-catalyzed tandem reactions were developed for the synthesis of dihydroisobenzofuran and Indanone derivatives from 2-triazole-benzaldehydes and 2-triazole-alkylaryl ketones. Dihydroisobenzofuran derivatives were obtained in good yields with high regioselectivities when alcohols were used as nuclophiles in these reactions, whereas the replacement of the alcohol with water resulted in the diastereoselective formation of highly functionalized Indanone derivatives.
Qingwei Meng - One of the best experts on this subject based on the ideXlab platform.
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asymmetric α hydroxylation of β Indanone esters and β Indanone amides catalyzed by c 2 substituted cinchona alkaloid derivatives
Advanced Synthesis & Catalysis, 2016Co-Authors: Yakun Wang, Hang Yin, Hai Qing, Jingnan Zhao, Qingwei MengAbstract:The highly catalytic asymmetric α-hydroxylation of β-Indanone esters and β-Indanone amides using peroxide as the oxidant was realized with a new C-2′ substituted Cinchona alkaloid derivatives. The two enantiomers of α-hydroxy-β-Indanone esters could be obtained by simply changing the oxidant. This protocol allows a convenient access to the corresponding α-hydroxy-β-Indanone esters and α-hydroxy-β-Indanone amides with up to 99% yield and 98% ee.
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Asymmetric α‐Hydroxylation of β‐Indanone Esters and β‐Indanone Amides Catalyzed by C‐2′ Substituted Cinchona Alkaloid Derivatives
Advanced Synthesis & Catalysis, 2016Co-Authors: Yakun Wang, Hang Yin, Hai Qing, Jingnan Zhao, Qingwei MengAbstract:The highly catalytic asymmetric α-hydroxylation of β-Indanone esters and β-Indanone amides using peroxide as the oxidant was realized with a new C-2′ substituted Cinchona alkaloid derivatives. The two enantiomers of α-hydroxy-β-Indanone esters could be obtained by simply changing the oxidant. This protocol allows a convenient access to the corresponding α-hydroxy-β-Indanone esters and α-hydroxy-β-Indanone amides with up to 99% yield and 98% ee.
Xuegong She - One of the best experts on this subject based on the ideXlab platform.
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PtI2-Catalyzed tandem 3,3-rearrangement/Nazarov reaction of arylpropargylic esters: synthesis of Indanone derivatives
Organic & biomolecular chemistry, 2011Co-Authors: Huaiji Zheng, Juan Yang, Changgui Zhao, Peng Jing, Bowen Fang, Xingang Xie, Xuegong SheAbstract:An efficient PtI2-catalyzed tandem reaction of arylpropargylic esters, involving 3,3-rearrangement and Nazarov reaction, has been developed to produce 3-substituted and 3,3-disubstituted Indanone derivatives. This approach provided a pathway to the synthesis of Indanone skeletons in natural products.
