基本信息
周鸣强  男  博导  中国科学院成都有机化学研究所
电子邮件: screenfilm@foxmail.com
通信地址: 成都市人民南路四段九号
邮政编码:

招生信息

   
招生专业
070303-有机化学
招生方向
有机合成方法学,药物合成

教育背景

2011-09--2015-07   中国科学院成都有机化学研究所   博士学位
2005-09--2008-07   四川大学华西药学院   硕士学位
2000-09--2004-07   四川大学华西公共卫生学院   学士学位

工作经历

   
工作简历
2011-09~2015-07,中国科学院成都有机化学研究所, 博士学位
2005-09~2008-07,四川大学华西药学院, 硕士学位
2000-09~2004-07,四川大学华西公共卫生学院, 学士学位
社会兼职
2022-04-30-2025-07-31,四川大学华西药学院产业导师, 四川大学华西药学院产业导师
2018-12-01-今,硕士研究生导师, 硕士研究生导师
2018-06-19-2021-06-18,遵义医科大学制药工程硕士研究生导师, 硕士研究生导师

教授课程

硕士研究生学术汇报

专利与奖励

   
奖励信息
(1) 手性药物中间体(S)-2-羟基-4-N-邻苯二甲酰胺基丁酸(PHBA)的中试新技术开发, 三等奖, 市地级, 2015
专利成果
( 1 ) 光学活性3,4-二氢-2H-1-苯并吡喃-2-羧酸和3,4-二氢-4-氧-2H-1-苯并吡喃-2-羧酸类化合物的制备方法, 2011, 第 2 作者, 专利号: CN101531651B

( 2 ) 一种3,4-二氢-4-氧-2H-1-苯并吡喃-2-羧酸类化合物的制备方法, 2008, 第 2 作者, 专利号: CN101121707A

出版信息

   
发表论文
(1) 碘化亚铜催化5-乙炔基噁唑-2,4二酮与苯甲酰乙腈的 脱羧[3+2]环加成反应, 2023, 第 5 作者
(2) 硫代靛红衍生的三氟乙基酮亚胺的合成, 2023, 通讯作者
(3) 对醌胺与2-硝基苯并呋喃的去芳构化[3+2]环加成反应, 2023, 通讯作者
(4) 苯并噻吩衍生的三氟乙基酮亚胺的合成, 2023, 通讯作者
(5) 氘代抗心血管病药物的合成研究进展, 2023, 第 5 作者
(6) Catalytic asymmetric dearomative [4 + 2] annulation of 2-nitrobenzofurans and 5H-thiazol-4-ones: stereoselective construction of dihydrobenzofuran-bridged polycyclic skeletons., Org. Chem. Front., 2022, 第 7 作者
(7) alpha-Nitrosostyrenes as Three-Atom Units for the (3+1) Cyclization Reaction: Facile Access to 2,3-Dihydrodiazete N-Oxides and Their Diversified Synthetic Conversions., Org. Lett., 2022, 第 5 作者
(8) Catalytic enantioselective hydrophosphinylation of in situ-generated indole-derived vinylogous imines to access 3-(1-diphenylphosphoryl-arylmethyl)indoles, CHEMICAL COMMUNICATIONS, 2022, 第 7 作者
(9) Catalytic asymmetric aromatizing inverse electron-demand [4+2] cycloaddition of 1-thioaurones and 1-azaaurones., Chem. Commun., 2022, 通讯作者
(10) DBU-catalyzed dearomative annulation of 2-pyridylacetates with α,β-unsaturated pyrazolamides for the synthesis of multisubstituted 2,3-dihydro-4H-quinolizin-4-ones., Org. Chem. Front., 2022, 通讯作者
(11) FIP-promoted intramolecular dearomative annulation of pyridylacetate derivatives to access functionalized 3,4-dihydroquinolizin-2-ones, Tetrahedron, 2022, 第 5 作者
(12) Copper-Catalyzed Ring-Opening (3+2) Annulation of Cyclopropenones with Ketoxime Acetates: Access to 1,2-Dihydro-pyrrol-3-ones Bearing a Quaternary Carbon Center, Eur. J. Org. Chem, 2022, 第 6 作者
(13) Catalytic asymmetric coupling of vinylogous species via deconjugated butenolide addition to vinylogous imines in situ generated from arylsulfonyl indoles, CHEMICAL COMMUNICATIONS, 2021, 第 7 作者
(14) A cascade deprotonation/intramolecular aldol reaction of alpha-carbonyl sulfonium ylides with 2-mercaptoindole-3-carbaldehydes and 2-mercaptobenzaldehydes to access thieno2,3-bindoles and benzothiophenes, ORGANIC & BIOMOLECULAR CHEMISTRY, 2021, 第 6 作者
(15) Copper-Catalyzed Decarboxylative 3+2 Annulation of Ethynylethylene Carbonates with Azlactones: Access to gamma-Butyrolactones Bearing Two Vicinal Quaternary Carbon Centers, JOURNAL OF ORGANIC CHEMISTRY, 2021, 第 6 作者
(16) Cyclocondensation of coumarin-3-thioformates with 3-hydroxyoxindoles and 3-aminooxindoles for the synthesis of spiro-fused pentaheterocyclic compounds, ORGANIC CHEMISTRY FRONTIERS, 2020, 第 6 作者
(17) Asymmetric dearomatization of 2-nitrobenzofurans by organocatalyzed one-step Michael addition to access 3,3 '-disubstituted oxindoles, CHEMICAL COMMUNICATIONS, 2020, 第 6 作者
(18) Coumarin-3-formylpyrazoles as 3-carbon synthons in cyclocondensation for the synthesis of spiro-fused pentacyclic spirooxindoles, ORGANIC & BIOMOLECULAR CHEMISTRY, 2020, 第 6 作者
(19) Catalytic asymmetric 4+2 cycloaddition of 1-((2-aryl)vinyl)naphthalen-2-ols with in situ generated ortho-quinone methides for the synthesis of polysubstituted chromanes, CHEMICAL COMMUNICATIONS, 2020, 第 7 作者
(20) 4+1 annulation reaction of cyclic pyridinium ylides with in situ generated azoalkenes for the construction of spirocyclic skeletons, ORGANIC & BIOMOLECULAR CHEMISTRY, 2020, 第 5 作者
(21) 4+2 Annulation Reaction of In Situ Generated Azoalkenes with Azlactones: Access to 4,5-Dihydropyridazin-3(2H)-Ones, JOURNAL OF ORGANIC CHEMISTRY, 2020, 第 6 作者
(22) Efficient construction of polycyclic chromans through 4-methylbenzenesulfonic acid mediated domino 1,6-addition/oxa-Mannich reaction of ortho-hydroxyphenyl substituted para-quinone methides and cyclic enamides, TETRAHEDRON, 2019, 第 5 作者
(23) Organocatalytic enantioselective sulfa-Michael addition of thiocarboxylic acids to beta-trifluoromethyl-alpha,beta-unsaturated ketones for the construction of stereogenic carbon center bearing a sulfur atom and a trifluoromethyl group, TETRAHEDRON, 2019, 第 4 作者
(24) Organocatalyzed Dearomative Cycloaddition of 2-Nitrobenzofurans and Isatin-Derived Morita-Baylis-Hillman Carbonates: Highly Stereoselective Construction of Cyclopentabbenzofuran Scaffolds, ORGANIC LETTERS, 2019, 第 6 作者
(25) Organocatalytic asymmetric 3+2-cycloaddition of 3-isothiocyanato oxindoles with 1,3,5-trisubstituted-hexahydro-1,3,5-triazines to access spiro-imidazolidinethione-oxindoles, TETRAHEDRON, 2019, 第 5 作者
(26) 奥美拉唑关键中间体杂质5-甲氧基苯并d噁唑-2(3H)-硫酮的分离及结构确证, Separation and Structural Confirmation of 5-Methoxybenzodoxazole-2(3H)-thione from Key, 合成化学, 2018, 第 2 作者
(27) One-pot access to indolychro meno [2,3-b]indoles via iodine- mediated Friedel-Crafts alkyl ation/oxidative coupling reaction of indoles and Salicylalde hydes, TETRAHEDRON, 2018, 通讯作者
(28) 抗抑郁药艾司西酞普兰的合成工艺改进, Process Improvement on The Synthesis of Antidepressant Escitalopram, 合成化学, 2018, 第 3 作者
(29) Base-catalyzed bis-sulfenyl ation of gamma-substituted butenolides for the synthesis of alpha-bisthio functionalized butenolide derivatives, Tetrahedron, 2017, 通讯作者
(30) Base-catalyzed bis-sulfenylation of gamma-substituted butenolides for the synthesis of alpha,alpha-bisthiofunctionalized butenolide derivatives, TETRAHEDRON, 2017, 通讯作者
(31) 酒石酸酯化物的合成与应用研究进展, Research Progress of Synthesis and Applications of Tartaric Esters, 合成化学, 2016, 第 3 作者
(32) 降血脂药环丙贝特的合成, Synthesis of Hypolipidemic Ciprofibrate, 合成化学, 2016, 第 4 作者
(33) Organocatalytic asymmetric michael/friedel-crafts cascade reaction of 3-pyrrolyl-oxindoles and alpha,beta-unsaturated aldehydes for the construction of chiral spiro5,6-dihydropyrido1,2-apyrrole-3,3 '-oxindoles, JOURNAL OF ORGANIC CHEMISTRY, 2015, 第 3 作者
(34) Preparation of 3-Sulfonylated 3,3-Disubstituted Oxindoles by the Addition of Sulfinate Salts to 3-Halooxindoles, JOURNAL OF ORGANIC CHEMISTRY, 2015, 第 4 作者
(35) Synthesis of furoxan derivatives: DABCO-mediated cascade sulfonylation/cyclization reaction of alpha-nitro-ketoximes, TETRAHEDRON, 2015, 第 2 作者
(36) Asymmetric Michael/Cyclization Cascade Reaction of 3-Isothiocyanato Oxindoles and 3-Nitroindoles with Amino-Thiocarbamate Catalysts: Enantioselective Synthesis of Polycyclic Spirooxindoles, ORGANIC LETTERS, 2015, 第 2 作者
(37) Dmap-catalyzed diels-alder reaction of 3-hydroxy-2-pyrone and methyleneindolinones for the synthesis of spirocyclic oxindolesl, TETRAHEDRON, 2015, 第 1 作者
(38) Organocatalytic asymmetric double Michael reaction of Nazarov reagents with alkylidene azlactones for the construction of spiro-fused cyclohexanone/5-oxazolone system, TETRAHEDRON, 2014, 第 1 作者
(39) Tandem Michael Addition-Ring Transformation Reactions of 3-Hydroxyoxindoles/3-Aminooxindoles with Olefinic Azlactones: Direct Access to Structurally Diverse Spirocyclic Oxindoles, JOURNAL OF ORGANIC CHEMISTRY, 2014, 第 4 作者
(40) 非达司他的合成新方法, A Novel Synthesis of Fidarestat, CHINESE JOURNAL OF ORGANIC CHEMISTRY, 2011, 第 4 作者
(41) 非达司他的合成新方法, A Novel Synthesis of Fidarestat, CHINESE JOURNAL OF ORGANIC CHEMISTRY, 2011, 第 4 作者
(42) N-乙基-N-甲基氨基甲酰氯的简便合成, A convenient synthesis of N- ethyl -N- methylcarbamoyl chloride, 华西药学杂志, 2008, 第 2 作者
(43) 重酒石酸利斯的明的合成, Synthesis of Rivastigmine Hydrogen Tartrate, 中国医药工业杂志, 2007, 第 2 作者
(44) 恩曲他滨顺式和反式消旋体的简便合成, A facile synthesis of cis and trans - ( ± ) - isomer of Emtricitabine, 华西药学杂志, 2007, 第 1 作者
(45) 盐酸替扎尼定的合成改进, Improved synthesis of tizanidine hydrochloride, 中国新药杂志, 2006, 第 3 作者

科研活动

   
科研项目
( 1 ) 3-硝基苯并杂环的不对称去芳香化反应在构建复杂多环化合物中的应用研究, 负责人, 国家任务, 2017-01--2019-12
( 2 ) 抗凝血药物达比加群酯工业化制备工艺的开发, 负责人, 中国科学院计划, 2016-06--2018-06
( 3 ) 汉防己甲素全合成研究, 负责人, 境内委托项目, 2018-03--2021-03
( 4 ) 克拉霉素合成工艺改进, 负责人, 境内委托项目, 2019-03--2020-12
( 5 ) 药物乙酰半胱氨酸合成工艺开发, 负责人, 境内委托项目, 2020-06--2020-12
( 6 ) 药物他唑巴坦酸杂质合成研究, 负责人, 境内委托项目, 2021-04--2021-08
( 7 ) 碳酸二甲酯合成关键催化剂配体合成工艺开发, 负责人, 研究所自主部署, 2021-05--2021-12
( 8 ) 乙酰半胱氨酸合成工艺开发, 负责人, 境内委托项目, 2020-05--2021-10
( 9 ) 红霉素肟绿色合成工艺开发, 负责人, 境内委托项目, 2020-01--2020-12
( 10 ) 原料药盐酸苄丝肼工艺开发, 负责人, 境内委托项目, 2023-03--2023-12