个人简历

孟祥太，教授，硕士生导师，2009年毕业于南开大学，2006年获得南开大学硕士学位，2009年获得南开大学化学系博士学位，2009年-2012年先后在大阪大学、东京大学做博士后研究，2012年，开始任教于天津理工大学化学化工学院，主要从事有机小分子的催化串联反应，在Angew. Chem., Int. Ed.; Chem. Commun; Org. Let.; J. Org. Chem; Chem. Eur. J;等杂志上发表学术论文20余篇

研究领域

"""""1. 有机小分子催化的串联反应研究\r
2. 鸟嘌呤核苷衍生物的合成以及自组装性质研究\r
3. 过渡金属催化的C-H键活化反应的研究"

近期论文

Deng, Q.; Yu, A.; Zhang, L.; Meng, X. Selective Synthesis of Benzothiophene‐Fused Polycyclic, Eight‐Membered N‐Heterocycles via Amine‐Mediated Three‐Component Domino Strategy. Adv. Synth. Catal. 2021.https://doi.org/10.1002/adsc.202001129\r
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Deng, Q.; Yu, A.; Li, M.; Meng, X. Amines‐Mediated Domino Reaction of Thioisatins: Synthesis of Benzothiophene fused N‐Heterocycles under Catalyst‐Free Conditions. Asian J. Org. Chem. 2021.https://doi.org/10.1002/ajoc.202000626\r
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Shen, J.; Yu, A.; Zhang, L.; Meng, X. Construction of benzothiophene fused pyrrolidone in water via a catalyst-free process and a mechanism study. Green Chem. 2020, 22, 6798-6803.\r
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Ma, S.; Yu, A.; Zhang, S.; Zhang, L.; Meng, X. Construction of [6-5-5-6-6] Pentacyclic Skeleton via a Phosphine-Catalyzed Domino Reaction and Mechanism Study. J. Org. Chem. 2020, 85, 7884-7895.\r
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Deng, Q.; Yu, A.; Zhou, J.; Cao, Q.; Meng, X. Construction of Benzothiophene or Benzothiopheno[2,3-e]azepinedione Derivatives via Three-Component Domino or One-Pot Sequences. J. Org. Chem. 2020, 85, 12270-12283.\r
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Deng, Q.; Meng, X. Recent Advances in the Cycloaddition Reactions of 2-Benzylidene-1-benzofuran-3-ones, and Their Sulfur, Nitrogen and Methylene Analogues. Chem. Asian. J. 2020, 15, 2838-2853.\r
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Li, K.; Wang, L.; Yu, A.; Zhu, L.; Zhang, L.; Gu, Y.; Meng, X. Synthesis of Benzothiophene-Fused Oxa[6.6.5]tricyclic Skeletons through a Cinchonidine- or NaOH-Promoted Quadruple Domino Sequence. Chem. Eur.J. 2019, 25, 9665-9669.\r
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Ding, W.; Yu, A.; Zhang, L.; Meng, X. Construction of Eight-Membered Cyclic Diaryl Sulfides via Domino Reaction of Arynes with Thioaurone Analogues and DFT Study on the Reaction Mechanism. Org. Lett. 2019, 21, 9014-9018.\r
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Shen, J.; Yang, Y.; Hou, X.; Zeng, W.; Yu, A.; Zhao, X.; Meng, X. Darzens reaction of thioisatins and sulfonium salts: approach to the synthesis of thiochromenone derivatives with anticancer potency. Org. Biomol. Chem. 2018, 16, 3487-3494.\r
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Ma, S.; Yu, A.; Zhang, L.; Meng, X. Phosphine-Catalyzed Domino Reaction of Thioaurones and Allenoate: Synthesis of Benzothiophene-Fused Dioxabicyclo[3.3.1]nonane Derivatives. J. Org. Chem. 2018, 83, 5410-5419.\r
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Ma, S.; Yu, A.; Meng, X. Phosphine-catalyzed [4 + 2] annulation of γ-benzyl allenoates: facile synthesis of benzothieno[3,2-b]pyran derivatives. Org. Biomol. Chem. 2018, 16, 2885-2892.\r
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Li, K.; Yu, A.; Meng, X. Synthesis of Dibenzothiophene and 1,4-Dihydrodibenzothiophene Derivatives via Allylic Phosphonium Salt Initiated Domino Reactions. Org. Lett. 2018, 20, 1106-1109.\r
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Ding, W.; Zhang, Y.; Yu, A.; Zhang, L.; Meng, X. Substrate-Controlled Domino Reactions of Crotonate-Derived Sulfur Ylides: Synthesis of Benzothiophene Derivatives. J. Org. Chem. 2018, 83, 13821-13833.\r
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Zhang, Y.; Yu, A.; Jia, J.; Ma, S.; Li, K.; Wei, Y.; Meng, X. NaH promoted [4+3] annulation of crotonate-derived sulfur ylides with thioaurones: synthesis of 2,5-dihydrobenzo[4,5]thieno[3,2-b]oxepines. Chem. Commun. 2017, 53, 10672-10675.\r
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Meng, X.; Du, Y.; Zhang, Q.; Yu, A.; Zhang, Y.; Jia, J.; Liu, X. Direct Functionalization of Azepane via Azomethine Ylides: A Highly Efficient Synthesis of Spirooxindoles Bearing a 1-Azabicyclo[5.3.0]decane Moiety. Asian J. Org. Chem. 2017, 6, 1719-1723.\r
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Jia, J.; Yu, A.; Ma, S.; Zhang, Y.; Li, K.; Meng, X. Solvent-Controlled Switchable Domino Reactions of MBH Carbonate: Synthesis of Benzothiophene Fused α-Pyran, 2,3-Dihydrooxepine, and Oxatricyclodecene Derivatives. Org. Lett. 2017, 19, 6084-6087.\r
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Du, Y.; Yu, A.; Jia, J.; Zhang, Y.; Meng, X. Direct N-H/α,α,β,β-Csp3-H functionalization of piperidine via an azomethine ylide route: synthesis of spirooxindoles bearing 3-substituted oxindoles. Chem. Commun. 2017, 53, 1684-1687.\r
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Liu, Y.; Du, Y.; Yu, A.; Mu, H.; Meng, X. DABCO-catalyzed unusual [4 + 2] cycloaddition reaction: non-substituted allenoate acts as a four-carbon synthon and facile synthesis of spirooxindoles. Org. Biomol. Chem. 2016, 14, 1226-1230.\r
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Du, Y.; Yu, A.; Zhang, Y.; Jia, J.; Meng, X. Cs2CO3-Promoted Michael Addition-[2,3]-Sigmatropic Rearrangement Domino Reaction: Facile Synthesis of a 3-Substituted Indoles Bearing a Homoallyl Sulfide Moiety. Asian J. Org. Chem. 2016, 5, 1309-1313.\r
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Liu, Y.; Du, Y.; Yu, A.; Qin, D.; Meng, X. Diverse synthesis of pyrano[2,3-b]indol and dihydropyrano[2,3-b]indol via tunable Lewis bases catalyzed domino reactions. Tetrahedron. 2015, 71, 7706-7716.\r
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Du, Y.; Liu, Y.; Yu, A.; Qin, D.; Zhang, K.; Meng, X. A Catalyst-Free Approach to Construct 3-(Cyclopentenone)oxindoles Through a Phosphine-Ylide-Initiated Triple Domino Sequence. Asian J. Org. Chem. 2015, 4, 630-637.\r
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Liu, Y.; Zhang, Q.; Du, Y.; Yu, A.; Zhang, K.; Meng, X. Convenient synthesis of substituted tetrahydrofuran via Lewis base catalyzed [3 + 2] domino reactions. RSC Adv. 2014, 4, 52629-52632