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REACTION: 作品数：2314被引量：2612H指数：16; 导出分析报告; 相关领域：理学更多>>; 相关作者：杨学明戴东旭王秀岩杨明晖吴国荣更多>>; 相关机构：中国科学院兰州大学中国科学院大学浙江大学更多>>; 相关期刊：更多>>; 相关基金：国家自然科学基金国家重点基础研究发展计划中国博士后科学基金高等学校学科创新引智计划更多>>

Highly Stable Binary Cross-Linkable Organic Nonlinear Optical Materials Using Different Acceptors Based on Huisgen Cycloaddition Reaction: 《Chinese Journal of Chemistry》2024年第24期3219-3226,共8页Yu Zhang Weijun Zhang Shuhui Bo Wenlong He Chuying Liu Jiahai Wang Fenggang Liu; supported by the Guangzhou Municipal Science and Technology Project(No.202102010426);the National Natural Science Foundation of China(Nos.21805049 and 22074025);Engineering Research Centre of Photonic Design Software,Ministry of Education,China(No.62175267).; How to obtain organic electro-optic materials with large electro-optic coefficients,high glass transition temperature,and good optical transparency remains a challenge in this field.To solve this problem,we introduce ...; 关键词：Nonlinear optical materials Electro-optic coefficient Long-term stability Huisgen cycloaddition Binary cross-linking

Enantioselective Construction of Polycyclic Chromanes through Organocatalytic Sequential Quintuple Reaction via One-Pot Step-Wise Procedure: 《Chinese Journal of Chemistry》2024年第18期2197-2202,共6页Jie Wang Hang Qin Ya-Li Song Fei Cao Zhi-Hao You; supported by the Advanced Talents Incubation Program of Hebei University(521000981411);the National Nature Science Foundation of China(82273792),Science Research Project of Hebei Education Department(QN2021023);the Natural Science Interdisciplinary Research Program of Hebei_University(DXK201913);High-throughput Intelligent Integrated Lung Cancer Targeted Drug Development Innovation Team Project(IT2023c01);the Excellent Youth Research Innovation Team of Hebei University(QNTD202406).; An efficient and highly stereoselective synthetic method to access polycyclic chromanes has been achieved through organocatalyzed one-pot step-wise reactions involving 2-hydroxycinnamaldehydes,2-aminochalcones,and mal...; 关键词：Asymmetric catalysis ORGANOCATALYSIS Cyclization Quintuple reaction POLYCYCLES HETEROCYCLES Chromane One-pot reaction

Synthesis of Diverse Oxetane Amino Acids via Visible-Light-Induced Photocatalytic Decarboxylative Giese-Type Reaction: 《Chinese Journal of Chemistry》2024年第12期1341-1346,共6页Haoliang Shi Yi Wan Yongqiang Zhang; Financial support from the program of the National Natural Science Foundation of China(21871086 and 22171080,Y-Q.Z.);Natural Science Foundation of Shanghai(23ZR1417200,Y.-Q.Z.)isgratefullyacknowledged.; The divergent synthesis of versatile 3,3′-disubstituted oxetane amino acids by utilizing visible-light-induced photocatalytic decarboxylative Giese-type reaction has been demonstrated.3-Methyleneoxetane-derived subst...; 关键词：Photoredox catalysis Decarboxylative Giese-type reaction Oxetane amino acids Amino acids Synthesis Radical reactions

Asymmetric Two-Component Alkenyl Catellani Reaction for the Construction of C—N Axial Chirality: 《Chinese Journal of Chemistry》2024年第7期699-704,共6页Chenggui Wu Ze-Shui Liu Yong Shang Chang Liu Shuang Deng Hong-Gang Cheng Hengjiang Cong Yinchun Jiao Qianghui Zhou; Herein,we report an asymmetric two-component alkenyl Catellani reaction for the construction of C—N axial chirality through a palladium/chiral norbornene cooperative catalysis and an axial-to-axial chirality transfer...; 关键词：Alkenyl Catellani reaction Asymmetric catalysis ATROPISOMERISM Axial-to-axial chirality transfer HETEROCYCLES

Design, Synthesis and Application of Multifunctional Chiral Aminophosphine Catalyst for Asymmetric Intermolecular Cross Rauhut-Currier Reaction: 《Chinese Journal of Chemistry》2022年第17期2061-2066,共6页Wu-Wei Dong Kui Tian Xiu-Qin Dong Chun-Jiang Wang; support from the National Natural Science Foundation of China(Grant Nos.22071186,22071187);the Natural Science Foundation of Hubei Province(Grant Nos.2020CFA036,2021CFA069);the Natural Science Foundation of Jiangsu Province(Grant No.BK20190213);the Fundamental Research Funds for the Central Universities(Grant No.2042022kf1180).; A series of structurally novel multifunctional chiral aminophosphine catalysts were developed through a concise synthetic strategy from easily available starting materials.The highly enantioselective intermolecular cr...; 关键词：Asymmetric catalysis Chiral aminophosphine Intermolecular cross Rauhut-Currier reaction Chiral multicarbonyl molecules Enantioselectivity

Machine Learning Prediction of Structure-Performance Relationship in Organic Synthesis被引量：1: 《Chinese Journal of Chemistry》2022年第17期2106-2117,共12页Li-Cheng Yang Lu-Jing Zhu Shuo-Qing Zhang Xin Hong; support fromthe National Natural Science Foundation of China(21873081and 22122109,X.H.,22103070,S.-Q.Z.);the Starry Night Science Fund of Zhejiang University Shanghai Institute for Advanced Study(SN-ZJU-SIAS-006,X.H.);Beijing National Laboratory for Molecular Sciences(BNLMS202102,X.H.);the Centerof Chemistry for Frontier Technologies and Key Laboratory of Precise Synthesis of Functional Molecules of Zhejiang Province(PSFM 2021-01,X.H.);the State Key Laboratory of Clean Energy Utilization(ZJUCEU2020007,X.H.);CAS Youth Interdisciplinary Team(JCTD-2021-11,X.H.)。; Data-driven approach has emerged as a powerful strategy in the construction of structure-performance relationships in organic synthesis.To close the gap between mechanistic understanding and synthetic prediction,we ha...; 关键词：Reaction performance prediction Synthesis design Structure-activity relationships Synthetic database Radical reactions

Visually Intracellular Detection of Telomerase Activity Based on DNA Strand Displacement Reaction and Gold Nanoparticle Labeling被引量：1: 《Chinese Journal of Chemistry》2022年第6期693-698,共6页Yajun Zhang Shen Yan Zhaoxin Chen Xin Jiang Shuang Rao Zhuoran Jiang Shanshan Qin Xiang Zhou Yuhao Du; supported by the National Natural Science Foundation of China(Grant No.22037004)。; Telomerase,which is regarded as a common biomarker for early cancer diagnostics and a potential target for clinical therapies,has attracted considerable interests concerning its detection and monitoring.Herein,we prop...; 关键词：TELOMERASE Nanoparticles DNA strand displacement INTRACELLULAR FRET

Polymer Synthesis Based on Self-Accelerating 1,3-Dipolar Cycloaddition Click Reactions: 《Chinese Journal of Chemistry》2021年第11期3093-3100,共8页Qingquan Tang Ke Zhang; Generous support was primarily provided by the National National Science Foundation of China(Nos.21871273,21622406 and 22001199).; This review reports our recent work on developing polymer synthesis methods based on a self-accelerating double-strain-promoted 1,3-dipole-alkyne cycloaddition(DSPDAC)click reaction.In DSPDAC,the cycloaddition of 1,3-...; 关键词：POLYMERIZATION Self-accelerating reaction Click chemistry Cyclic polymer Reactive intermediates

Catellani Reaction: An Enabling Technology for Vicinal Functionalization of Aryl Halides by Palladium(o)/Norbornene Cooperative Catalysis: 《Chinese Journal of Chemistry》2021年第6期1690-1705,共16页Sichan Dong Xinjun Luan; the National Natural Science Foundation of China(21925108,21672169);the Key Science and Technology Innovation Team of Shaanxi Province(2017KCT-37);the Key Laboratory Project of Xi'an(201805058ZD9CG42)for financial support.; The Catellani reaction,originally discovered by Catellani in 1997,and further developed by Catellani,Lautens and others,has emerged as a powerful strategy for the synthesis of polysubstituted arenes,which would be dif...; 关键词：Catellani reaction PALLADIUM Domino reaction C-H activation Vicinal functionalization

Transition Metal Catalyzed Enantioselective Borylative Cyclization Reactions被引量：1: 《Chinese Journal of Chemistry》2021年第2期391-401,共11页Yuqi Ji Min Zhang Mimi Xing Huanhuan Cui Qian Zhao Chun Zhang; Financial support from Tianjin University and the National Natural Science Foundation of China(No.21801181)is acknowledged.; Due to the significance of corresponding products,enantioselective borylative cyclization reactions have been studied intensively in recent years.Many groups have developed efficient methods to transform unsaturated s...; 关键词：Asymmetric synthesis Transition metal catalysis Boronation reaction Cyclization reaction ENANTIOSELECTIVITY

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