The Experts below are selected from a list of 249 Experts worldwide ranked by ideXlab platform
Cheng-he Zhou - One of the best experts on this subject based on the ideXlab platform.
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Sequential Michael addition/retro-Claisen condensation of aromatic β-Diketones with α,β-unsaturated esters: an approach to obtain 1,5-ketoesters.
Organic & biomolecular chemistry, 2016Co-Authors: Gui-xin Cai, Jing Wen, Ting-ting Lai, Dan Xie, Cheng-he ZhouAbstract:A K2CO3-catalyzed one-pot protocol involving sequential C–C bond formation and cleavage of aromatic β-Diketones with α,β-unsaturated esters is developed to obtain 1,5-ketoesters. The sequential reaction via Michael addition and retro-Claisen condensation proceeds smoothly under mild conditions in up to 98% isolated yield. The mechanism study disclosed that the cascade process involved C–C bond cleavage of aromatic β-Diketone as a phenacyl donor under alcoholic alkalescent conditions.
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sequential michael addition retro claisen condensation of aromatic β Diketones with α β unsaturated esters an approach to obtain 1 5 ketoesters
Organic and Biomolecular Chemistry, 2016Co-Authors: Gui-xin Cai, Jing Wen, Ting-ting Lai, Dan Xie, Cheng-he ZhouAbstract:A K2CO3-catalyzed one-pot protocol involving sequential C–C bond formation and cleavage of aromatic β-Diketones with α,β-unsaturated esters is developed to obtain 1,5-ketoesters. The sequential reaction via Michael addition and retro-Claisen condensation proceeds smoothly under mild conditions in up to 98% isolated yield. The mechanism study disclosed that the cascade process involved C–C bond cleavage of aromatic β-Diketone as a phenacyl donor under alcoholic alkalescent conditions.
Gui-xin Cai - One of the best experts on this subject based on the ideXlab platform.
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Sequential Michael addition/retro-Claisen condensation of aromatic β-Diketones with α,β-unsaturated esters: an approach to obtain 1,5-ketoesters.
Organic & biomolecular chemistry, 2016Co-Authors: Gui-xin Cai, Jing Wen, Ting-ting Lai, Dan Xie, Cheng-he ZhouAbstract:A K2CO3-catalyzed one-pot protocol involving sequential C–C bond formation and cleavage of aromatic β-Diketones with α,β-unsaturated esters is developed to obtain 1,5-ketoesters. The sequential reaction via Michael addition and retro-Claisen condensation proceeds smoothly under mild conditions in up to 98% isolated yield. The mechanism study disclosed that the cascade process involved C–C bond cleavage of aromatic β-Diketone as a phenacyl donor under alcoholic alkalescent conditions.
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sequential michael addition retro claisen condensation of aromatic β Diketones with α β unsaturated esters an approach to obtain 1 5 ketoesters
Organic and Biomolecular Chemistry, 2016Co-Authors: Gui-xin Cai, Jing Wen, Ting-ting Lai, Dan Xie, Cheng-he ZhouAbstract:A K2CO3-catalyzed one-pot protocol involving sequential C–C bond formation and cleavage of aromatic β-Diketones with α,β-unsaturated esters is developed to obtain 1,5-ketoesters. The sequential reaction via Michael addition and retro-Claisen condensation proceeds smoothly under mild conditions in up to 98% isolated yield. The mechanism study disclosed that the cascade process involved C–C bond cleavage of aromatic β-Diketone as a phenacyl donor under alcoholic alkalescent conditions.
Dan Xie - One of the best experts on this subject based on the ideXlab platform.
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Sequential Michael addition/retro-Claisen condensation of aromatic β-Diketones with α,β-unsaturated esters: an approach to obtain 1,5-ketoesters.
Organic & biomolecular chemistry, 2016Co-Authors: Gui-xin Cai, Jing Wen, Ting-ting Lai, Dan Xie, Cheng-he ZhouAbstract:A K2CO3-catalyzed one-pot protocol involving sequential C–C bond formation and cleavage of aromatic β-Diketones with α,β-unsaturated esters is developed to obtain 1,5-ketoesters. The sequential reaction via Michael addition and retro-Claisen condensation proceeds smoothly under mild conditions in up to 98% isolated yield. The mechanism study disclosed that the cascade process involved C–C bond cleavage of aromatic β-Diketone as a phenacyl donor under alcoholic alkalescent conditions.
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sequential michael addition retro claisen condensation of aromatic β Diketones with α β unsaturated esters an approach to obtain 1 5 ketoesters
Organic and Biomolecular Chemistry, 2016Co-Authors: Gui-xin Cai, Jing Wen, Ting-ting Lai, Dan Xie, Cheng-he ZhouAbstract:A K2CO3-catalyzed one-pot protocol involving sequential C–C bond formation and cleavage of aromatic β-Diketones with α,β-unsaturated esters is developed to obtain 1,5-ketoesters. The sequential reaction via Michael addition and retro-Claisen condensation proceeds smoothly under mild conditions in up to 98% isolated yield. The mechanism study disclosed that the cascade process involved C–C bond cleavage of aromatic β-Diketone as a phenacyl donor under alcoholic alkalescent conditions.
Ting-ting Lai - One of the best experts on this subject based on the ideXlab platform.
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Sequential Michael addition/retro-Claisen condensation of aromatic β-Diketones with α,β-unsaturated esters: an approach to obtain 1,5-ketoesters.
Organic & biomolecular chemistry, 2016Co-Authors: Gui-xin Cai, Jing Wen, Ting-ting Lai, Dan Xie, Cheng-he ZhouAbstract:A K2CO3-catalyzed one-pot protocol involving sequential C–C bond formation and cleavage of aromatic β-Diketones with α,β-unsaturated esters is developed to obtain 1,5-ketoesters. The sequential reaction via Michael addition and retro-Claisen condensation proceeds smoothly under mild conditions in up to 98% isolated yield. The mechanism study disclosed that the cascade process involved C–C bond cleavage of aromatic β-Diketone as a phenacyl donor under alcoholic alkalescent conditions.
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sequential michael addition retro claisen condensation of aromatic β Diketones with α β unsaturated esters an approach to obtain 1 5 ketoesters
Organic and Biomolecular Chemistry, 2016Co-Authors: Gui-xin Cai, Jing Wen, Ting-ting Lai, Dan Xie, Cheng-he ZhouAbstract:A K2CO3-catalyzed one-pot protocol involving sequential C–C bond formation and cleavage of aromatic β-Diketones with α,β-unsaturated esters is developed to obtain 1,5-ketoesters. The sequential reaction via Michael addition and retro-Claisen condensation proceeds smoothly under mild conditions in up to 98% isolated yield. The mechanism study disclosed that the cascade process involved C–C bond cleavage of aromatic β-Diketone as a phenacyl donor under alcoholic alkalescent conditions.
Jing Wen - One of the best experts on this subject based on the ideXlab platform.
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Sequential Michael addition/retro-Claisen condensation of aromatic β-Diketones with α,β-unsaturated esters: an approach to obtain 1,5-ketoesters.
Organic & biomolecular chemistry, 2016Co-Authors: Gui-xin Cai, Jing Wen, Ting-ting Lai, Dan Xie, Cheng-he ZhouAbstract:A K2CO3-catalyzed one-pot protocol involving sequential C–C bond formation and cleavage of aromatic β-Diketones with α,β-unsaturated esters is developed to obtain 1,5-ketoesters. The sequential reaction via Michael addition and retro-Claisen condensation proceeds smoothly under mild conditions in up to 98% isolated yield. The mechanism study disclosed that the cascade process involved C–C bond cleavage of aromatic β-Diketone as a phenacyl donor under alcoholic alkalescent conditions.
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sequential michael addition retro claisen condensation of aromatic β Diketones with α β unsaturated esters an approach to obtain 1 5 ketoesters
Organic and Biomolecular Chemistry, 2016Co-Authors: Gui-xin Cai, Jing Wen, Ting-ting Lai, Dan Xie, Cheng-he ZhouAbstract:A K2CO3-catalyzed one-pot protocol involving sequential C–C bond formation and cleavage of aromatic β-Diketones with α,β-unsaturated esters is developed to obtain 1,5-ketoesters. The sequential reaction via Michael addition and retro-Claisen condensation proceeds smoothly under mild conditions in up to 98% isolated yield. The mechanism study disclosed that the cascade process involved C–C bond cleavage of aromatic β-Diketone as a phenacyl donor under alcoholic alkalescent conditions.