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解沛忠

领域:新材料产业 学校:南京工业大学职称:副教授

有机合成化学和绿色化学...

具体了解该专家信息,请致电:027-87555799 邮箱 haizhi@uipplus.com

教育背景

2008-2013年就读于南开大学并获得博士学位(导师:黄有 教授, 陈茹玉 院士)

工作经历

2013-2014年在日本東京大学从事博士后研究(合作导师:Prof. Shū Kobayashi),2014年11月到南京工业大学工作

项目课题经历

主持国家自然科学基金和江苏省自然科学基金等研究项目

论文、成果、著作等

在Nat. Commun.等重要刊物发表文章30余篇。P. Xie*, S. Li, Y. Liu, X. Cai, J. Wang, X. Yang, T.-P. Loh*, Alkaline-earth Metal-Catalyzed Dehydrative Allylic Alkylation. Org. Lett. 2020, 22, 31-35. P. Xie*, X. Wo, X. Yang, X. Cai, S. Li, C. Gao, W. Fu, Z. Sun, T.-P. Loh*, Calcium-catalyzed Regioselective Dehydrative Cross-coupling of Propargylic Alcohols with 1,3-Dicarbonyl Compounds. Green Chem. 2019, 21, 5207. P. Xie*, W. Fu, X. Cai, Z. Sun, Y. Wu, S. Li, C. Gao, X. Yang, T.-P. Loh*, A Ba/Pd Catalytic System Enables Dehydrative Cross-Coupling and Excellent E-Selective Wittig Reactions. Org. Lett. 2019, 21, 7055. P. Xie*, W. Fu, Y. Wu, X. Cai, Z. Sun, S. Li, C. Gao, X. Yang, T.-P. Loh*, Allylic Phosphorus Ylides Directly Generated from Alcohols with Water as the Only Byproduct. Org. Lett. 2019, 21, 4168. P. Xie*, J. Wang, Y. Liu, J. Fan, X. Wo, W. Fu, Z. Sun, T.-P. Loh*, Water-promoted C-S bond formation reactions. Nat. Commun. 2018, 9, 1321. (Highlighted by K. J. Geogheghan, Nat. Rev. Chem. 2018, 2, 3). Y. Liu, P. Xie*, Z. Sun, X. Wo, C. Gao, W. Fu, T.-P. Loh*, Direct Substitution of Secondary and Tertiary Alcohols to Generate Sulfones under Catalyst and Additive-free Conditions. Org. Lett. 2018, 20, 5353. P. Xie*, J. Fan, Y. Liu, X. Wo, W. Fu, T.-P. Loh*, Bronsted acid/organic photoredox cooperative catalysis: Easy access to tri- and tetra-substituted alkenylphosphorus compounds from alcohols and P-H species. Org. Lett. 2018, 20, 3341. X. Wo, P. Xie*, W. Fu, C. Gao, Y. Liu, Z. Sun, T.-P. Loh*, Barium-Catalyzed C-OH/P-H Dehydrative Cross-coupling for C-P Bond Construction. Chem. Commun. 2018, 54, 11132. P. Xie*, J. Wang, J. Fan, Y. Liu, X. Wo, W. Fu, T.-P. Loh*, The C–OH/P–H dehydrative cross-coupling for ..the construction of the P–C bond under metal free conditions. Green Chem. 2017, 19, 2135. P. Xie*, L. Guo, L. Xu, T.-P. Loh*, Asymmetric P-C Bond Formation:Diastereoselective Synthesis of Adjacent P,C-Stereogenic Allylic Phosphorus Compounds. Chem. Asian J. 2016, 11, 1353. P. Xie, Y. Huang*, Morita-Baylis-Hillman Adduct Derivates (MBHADs): The Versatile Reactivity in Lewis Base-promoted Annulation. Org. Biomol. Chem. 2015, 13, 8578. (Review, ESI Highly Cited Paper) 独立工作之前发表论文: P. Xie, E. Li, J. Zheng, Y. Huang*, Sequential Catalyst Phosphine/Secondary Amine Promoted [1+4]/Rearrangement Domino Reaction for the Construction of (2H)-Pyrans and 2-Oxabicyclo[2.2.2]oct-5-ene Skeletons. Eur. J. Org. Chem. 2014, 1189. P. Xie, Y. Huang,* Cross-Rauhut-Currier Reactions Initiated Domino Annulations. Eur. J. Org. Chem. 2013, 6213. (Review, Invited by Editor) P. Xie, E. Li, J. Zheng, Y. Huang,* R. Chen, Tunable Phosphine-Mediated Domino Reaction: Selective Synthesis of 2,3-Dihydrofurans and Biaryls. Adv. Synth. Catal. 2013, 355, 161. (Hot Paper, Selected by Editor). P. Xie, Y. Huang,* R. Chen, Phosphine-Mediated Domino Benzannulation Strategy for the Construction of Highly Functionalized Multiaryl Skeletons. Chem. Eur. J. 2012,18, 7362. (Most Accessed in May 2012, Top 10) P. Xie, W. Lai, Z. Geng, Y. Huang,* R. Chen, Phosphine-Catalyzed Domino Reaction for the Synthesis of Conjugated 2,3- Dihydrofurans from Allenoates and Nazarov Reagents. Chem. Asian J. 2012, 7, 1533-1537. P. Xie#, L. Wang#, L. Yang, E. Li, J. Ma, Y. Huang,* R. Chen, Domino Reaction for the Chemo- and Stereoselective Synthesis of trans-2,3-Dihydrobenzofurans from N-Thiophosphinyl Imines and Sulfur Ylides. J. Org. Chem. 2011,76, 7699–7705. (#Equal contribution) P. Xie, Y. Huang,* W. Lai, X. Meng, Ruyu Chen, Bifunctional Phosphine -catalyzed cross-Rauhut–Currier/Michael/Aldol Condensation Triple Domino Reaction: Synthesis of Functionalized Cyclohexenes. Org. Biomol. Chem. 2011, 9, 6707–6714. P. Xie, Y. Huang,* R. Chen,* Phosphine-Catalyzed Domino Reaction: Highly Stereoselective Synthesis of trans-2,3-Dihydrobenzofurans from Salicyl N-Thiophosphinyl Imines and Allylic Carbonates. Org. Lett. 2010, 12, 3768-3771.

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