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張志國 簡介

時間:2015-07-11瀏覽:10756設(shè)置



       

張志國,,博士,,教授,,博士生導(dǎo)師,。1977 年生于黑龍江省延壽縣,,2012 年 09 月加入九·三學(xué)社,。河南省杰出青年科學(xué)基金,、吉林省優(yōu)秀博士學(xué)位論文獲得者,。先后獲得河南省教育廳學(xué)術(shù)技術(shù)帶頭人、河南省高??萍紕?chuàng)新人才,、河南省高校青年骨干教師、河南省優(yōu)秀博士后研究人員,、河南師范大學(xué)平原學(xué)者等榮譽稱號,。《Chin Chem Lett》編委,,《有機化學(xué)》青年編委,,《河南師范大學(xué)學(xué)報》(自然科學(xué)版) 青年編委,《能源與環(huán)?!非嗄昃幬?。

科研方面:主要從事含氮、氧等雜環(huán)類化合物的合成研究工作,,尤其是天然產(chǎn)物母核結(jié)構(gòu)的合成,。先后主持國家級項目 4 項 (包括:青年基金 1 項,面上項目 2 項,,國家博士后特別資助 1 項),,主持省部級項目 6 項 (包括:省杰出青年科學(xué)基金項目1項,省自然科學(xué)基金面上項目1項,,國家博士后面上項目1項,,省高校青年骨干教師項目1項,省科技創(chuàng)新人才計劃項目 1 項,,省基礎(chǔ)與前沿技術(shù)研究項目1項),。截止2023年09月,在Angew Chem Int Ed,、Chem Sci,、Green Chem、Org Lett 和 J Org Chem等國際學(xué)術(shù)期刊上發(fā)表SCI研究論文 89 篇,。其中,1 個研究工作被國際新藥研發(fā)企業(yè)“藥明康德”作為工具方法收錄,;2 個研究工作入選SCI高被引論文,;3 個研究工作被評論性期刊Synfacts雜志以亮點文章評價并推介;6 個研究工作被有機化學(xué)專業(yè)網(wǎng)站http://www.organic-chemistry.org/作為工具方法永久收錄并推介,。獲得河南省優(yōu)秀科技論文一等獎1項二等獎2項,,河南省自然科學(xué)論文一等獎 2  項。授權(quán)中國發(fā)明專利  12  件,。受邀擔(dān)任30余種SCI期刊的審稿人,。

教學(xué)方面:主要承擔(dān)本科生《有機化學(xué)實驗》和研究生《現(xiàn)代化學(xué)實驗技術(shù)》課程教學(xué),,也是“《有機合成化學(xué)》河南省高等學(xué)校雙語教學(xué)示范課程”和“《金屬有機化學(xué)》河南省高等學(xué)校雙語教學(xué)示范課程”的主要成員。

熱烈歡迎廣大有志從事有機化學(xué)的同學(xué)加盟,,一起用有機化學(xué)改變?nèi)松?,開創(chuàng)美好的明天!

ORCID:0000-0001-6920-0471

聯(lián)系電話:18951893592

E-mail:[email protected][email protected]

實驗室地址:河南師范大學(xué)西校區(qū)化學(xué)北樓N-608實驗室(你來或不來我都在這里等你?。?/span>


教育與研究經(jīng)歷:

1994年09月 – 1998年07月       黑龍江省延壽縣第一中學(xué)94-6班,。

1998年09月 – 2002年07月      牡丹江師范學(xué)院化學(xué)系,理學(xué)學(xué)士,。

2002年09月 – 2004年08月      河北懷安第一高級中學(xué),,化學(xué)教師。

2004年09月 – 2010年06月      東北師范大學(xué)化學(xué)學(xué)院,,碩博連讀,,理學(xué)博士。

2010年07月 – 2013年10月     河南師范大學(xué),,化學(xué)與化工學(xué)院,,教師,講師,。

2012年02月 – 2014年12月     河南師范大學(xué),,化學(xué)博士后科研流動站,博士后,。

2013年11月 – 2022年10月    河南師范大學(xué),,化學(xué)與化工學(xué)院,教師,,副教授,。

2022年11月 – 現(xiàn)在                河南師范大學(xué),化學(xué)化工學(xué)院,,教師,,教授。


領(lǐng)域與興趣:

有機合成化學(xué),;綠色合成化學(xué),;金屬有機化學(xué)


主持的科研項目:


1. 國家自然科學(xué)基金項目——面上項目,N-芳基酰胺類惰性C(aryl)-N鍵直接活化/官能化反應(yīng)研究,,21772032,,2018.01-2021.12,64萬元,,主持,。

2. 國家自然科學(xué)基金項目——面上項目,單芳基雙C-H官能化策略在苯[d]雜環(huán)衍生物合成中的應(yīng)用,,21272057,,2013.01-2016.12,,80萬元,主持,。

3. 國家自然科學(xué)基金項目——青年基金項目,,炔丙基全碳1,3-偶極子在構(gòu)建呋喃并雜環(huán)衍生物中的應(yīng)用,21002051,,2011.01-2013.12,,19萬元,主持,。

4. 河南省自然科學(xué)基金——杰出青年科學(xué)基金項目,,螺環(huán)化合物不對稱合成研究,222300420012,,2022.01-2024.12,,50萬元,主持,。

5. 中國博士后科學(xué)基金——特別資助項目,,呋喃并雜環(huán)合成新策略研究,2013T60701,,2013.06-2014.12,,15萬元,主持,。

6. 中國博士后科學(xué)基金——面上項目,,單芳基雙C-H官能化新策略制備幾種苯并雜環(huán)衍生物,2012M521397,,2012.11-2014.12,,5萬元,主持,。

7. 河南省自然科學(xué)基金——面上項目,,吡咯/呋喃/吡喃并喹啉類化合物的設(shè)計、合成與抗菌活性研究,,162300410180,,2017.01-2019.12,10萬元,,主持,。

8. 河南省教育廳科技創(chuàng)新人才支持計劃,幾種吡咯并雜環(huán)衍生物新合成策略研究,,17HASTIT002,2017.01-2018.12,,60萬元,,主持,,結(jié)題優(yōu)秀。

9. 河南省高等學(xué)校青年骨干教師資助計劃,,C(sp2)-H鍵活化/C(sp2)-N鍵形成反應(yīng)在合成角型的雜環(huán)并喹啉酮類化合物中的應(yīng)用,,2014GGJS-049,2015.01-2018.01,,4萬元,,主持。

10. 河南省基礎(chǔ)與前沿技術(shù)研究項目,,天然產(chǎn)物雜環(huán)母核合成新方法,,112300410312,2011.01-2013.12,,主持,。

11. 東北師范大學(xué)優(yōu)秀博士論文基金,幾種雜環(huán)并喹啉類生物堿的新合成策略研究,,2008-2010,,6萬元,主持,。


代表性論文(第一作者或者通訊作者)

1. Zhang, Z.; Zhang, Q.;* Sun, S.; Xiong, T.; Liu, Q.* Domino Ring-Opening/Recyclization Reactions of Doubly Activated Cyclopropanes as a Strategy for the Synthesis of Furoquinoline Derivatives. Angew. Chem. Int. Ed., 2007, 46, 1726-1729. https://doi.org/10.1002/anie.200604276

2. Zhang, Z.; Zhang, Q.;* Yan, Z.; Liu, Q.* One-Step Synthesis of the Tricyclic Core of Martinellic Acid from 2-(Cyanomethyl)-3-oxo-N-arylbutanamides. J. Org. Chem., 2007, 72, 9808-9810. https://doi.org/10.1021/jo701551f

3. Zhang, Q.;* Zhang, Z.; Yan, Z.; Liu, Q.,* Wang, T. A New Efficient Synthesis of Pyranoquinolines from 1-Acetyl N-Aryl Cyclopentanecarboxamides. Org. Lett., 2007, 9, 3651-3653. https://doi.org/10.1021/ol701536q

4. Xiong, T.; Zhang, Q.;* Zhang, Z.; Liu, Q.* A Divergent Synthesis of γ-Iminolactones, Dihydroquinolin-2-ones and γ-Lactames from β-Hydroxymethylcyclopropanylamides. J. Org. Chem., 2007, 72, 8005-8009. https://doi.org/10.1021/jo701495s

5. Zhang, Z.; Zhang, Q.;* Ni, Z.; Liu, Q.* Ag-containing all-carbon 1,3-dipoles: generation and formal cycloaddition for furo[3,2-b]-β/γ-lactams. Chem. Commun., 2010, 46, 1269-1271 (Highlight by SYNFACTS, Synfacts, 2010, 5, 0524). https://doi.org/10.1039/b917856b

6. Zhang, Z.;* Xue, C., Liu, X.; Zhang, Q.;* Liu, Q.* Synthesis of polysubstituted 3H-pyrimidin-4-ones from cyanoacetamides under Vilsmeier conditions. Tetrahedron, 2011, 67, 7081-7084. https://doi.org/10.1016/j.tet.2011.07.006

7. Zhang, Z.;* Fang, S.; Liu, Q.; Zhang, G.,* Microwave-assisted facile synthesis of furo[3,2-b]indole derivatives via silver(I)-mediated [3+2]?cycloaddition. Adv. Synth. Catal., 2012, 354 (5), 927-932. https://doi.org/10.1002/adsc.201100767

8. Zhang, Z.;* Fang, S.; Liu, Q.; Zhang, G.* Approach to polysubstituted 4-pyridones from N-aryl acetoacetamides via a N to C 1,3-acyl migration mediated by sodium persulfate. J. Org. Chem., 2012, 77 (17), 7665-7670. https://doi.org/10.1021/jo3010217

9. Bi, J.; Zhang, Z.;* Liu, Q.; Zhang, G.* Catalyst-free and highly selective electrophilic mono-fluorination of acetoacetamides: facile and efficient preparation of 2-fluoroacetoacetamides in PEG-400. Green Chem., 2012, 14 (4), 1159-1162. https://doi.org/10.1039/C2GC16661E


10. Zhang, Z.;* Bi, J.; Liu, Q.; Zhang, G.* The Synthesis of α,α-Difluoroacetamides via Electrophilic Fluorination in the Mixed-solvent of Water and PEG-400. J. Fluorine Chem., 2013, 151, 45-49. https://doi.org/10.1016/j.jfluchem.2013.03.016


11.Zhang, Z.;* Wang, D.; Wang, B.; Liu, Q.; Liu, T.; Zhang, W.; Yuan, B.; Zhao, Z.; Han, D.; Zhang, G.* SnCl4 Mediated synthesis of γ-amino ketones derivatives via the ring-opening reaction of 4,5-dihydropyrroles. Tetrahedron, 2013, 69, 9063. https://doi.org/10.1016/j.tet.2013.08.027

12. Li, Z.; Zhang, Z.;* Zhang, W.; Liu, Q.; Liu, T.; Zhang, G.* Copper-Mediated Sequential C-N and N-N Bond Formation: Facile Synthesis of Symmetrical 1,2,4-Triazoles. Synlett, 2013, 24, 2735-2739. https://doi.org/10.1055/s-0033-1338985

13. Zhang, Z.;* Qian, J.; Tain, Q.; Liu, T.; Liu, Q.; Zhang, G.* Oxidative Nuclear Bromination of Substituted 4-Pyridones Using Pyridinium Bromochromate. Synth. Commun., 2014, 44, 674-81. https://doi.org/10.1080/00397911.2013.834363

14. Zhang, Z.;* Zhang, W.; Li, J.; Liu, Q.; Liu, T.; Zhang, G.* Synthesis of Multisubstituted Pyrroles from Doubly Activated Cyclopropanes Using an Iron-Mediated Oxidation Domino Reaction. J. Org. Chem., 2014, 79, 11226–11233. https://doi.org/10.1021/jo5018487

15. Zhang, Z.;* Tian, Q.; Qian, J.; Liu, Q.; Liu, T.; Shi, L.; Zhang, G.,* Dimethyl Sulfoxide Participant Iron-Mediated Cascade Oxidation/alpha-Formylation Reaction of Substituted 2,3-Dihydropyrroles under Air and Protonic Acid Free Condition. J. Org. Chem.,2014,79, 8182-8188. https://doi.org/10.1021/jo501385w

16. Zhang, L.; Zhang, Z.;* Liu, Q.; Liu, T.; Zhang, G.* Iron-Catalyzed Vinylogous Aldol Condensation of Biginelli Products and Its Application toward Pyrido[4,3-d]pyrimidinones. J. Org. Chem., 2014, 79, 2281-2288. https://doi.org/10.1021/jo402773r

17. Qian, J.; Zhang, Z.;* Liu, Q.; Liu, T.; Zhang, G.* Dimethyl Sulfoxide Participating in Copper(I) Iodide-Catalyzed Cascade Oxidation/Formylation Reactions: The Synthesis of alpha-Formylpyrroles from 2,3-Dihydro-1H-pyrroles. Adv. Synth. Catal., 2014, 356, 3119-3124. https://doi.org/10.1002/adsc.201400332

18. Zhang, Z.;* Zhang, L.; Duan, X.; Yan, X.; Yan, Y.; Liu, Q.; Liu, T.; Zhang, G.* Iron-catalyzed four-member multicomponent reaction for assembly of (E)-6-arylvinyl-3,4-dihydropyrimidin-2(1H)-ones. Tetrahedron, 2015, 71, 7745-7751. https://doi.org/10.1016/j.tet.2015.07.039

19. Zhang, Z.;* Zhang, F.; Wang, H.; Wu, H.; Duan, X.; Liu, Q.; Liu, T.; Zhang, G.* Catalyst-Free Domino Reaction of 1-Acryloyl-1-N-arylcarbamylcyclopropanes with Amines: One-Pot Approach to 2,3,6,7-Tetrahydro-1H-pyrrolo[3,2-c]pyridin-4(5H)-ones. Adv. Synth. Catal., 2015, 357, 2681-2686. https://doi.org/10.1002/adsc.201500251

20. Zhang, Z.;* Li, J.; Zhang, G.;* Ma, N.; Liu, Q.; Liu, T. Iron-Catalyzed Intramolecular C(sp(2))-N Cyclization of 1-(N-Arylpyrrol-2-yl)ethanone O-Acetyl Oximes toward Pyrrolo[1,2-a]quinoxaline Derivatives. J. Org. Chem., 2015, 80, 6875-6884. https://doi.org/10.1021/acs.joc.5b00915

21. Kai Sun,* Xin Wang, Lulu Liu, Jingjing Sun, Zhiguo Zhang, Guisheng Zhang*, Copper-Catalyzed Cross-Dehydrogenative C?N Bond Formation of Azines with Azoles: Overcoming the Limitation of  Oxidizing N?O Activation Strategy, ACS Catal., 2015, 5, 7194. https://pubs.acs.org/doi/10.1021/acscatal.5b02411 

22.Zhang, Z.;* Yan, X.; Zhang, G.;* Liu, Q.; Ma, N.; Liu, T.; Shi, L. Copper(I)-catalyzed domino allylic C(sp3)–H aminative cyclization/oxidative reaction and its application toward pyrrolo[3,4-d]pyrimidinones. Tetrahedron, 2016, 72, 3077-3083. https://doi.org/10.1016/j.tet.2016.04.031

23. Zhang, Z.;* Qian, J.; Zhang, G.;* Ma, N.; Liu, Q.; Liu, T.; Sun, K.; Shi, L. Copper(I) catalyzed C(sp2)–N bond formation: synthesis of pyrrolo[3,2-c]quinolinone derivatives. Org. Chem. Front., 2016, 3, 344-348. https://doi.org/10.1039/C5QO00417A


24. Zhang, Z.;* Li, J.; Huang, G.; Sun, K.; Zhang, G.;* Ma, N.; Liu, Q.; Liu, T. Copper(I)-Catalyzed Intramolecular N-N Coupling of Cyclopropyl O-Acyl Ketoximes: Synthesis of Spiro-fused Pyrazolin-5-ones. Chin. J. Chem., 2016, 34, 1309-1320. https://doi.org/10.1002/cjoc.201600479


25. Yan, X.; Zhang, Z.;* Zhang, G.;* Ma, N.; Liu, Q.; Liu, T.; Shi, L. Copper(I)-catalysed amidation and successive oxidation of benzylic C(sp3)–H bond: synthesis of 1H-pyrrolo[3,4-b]quinoline-1,3(2H)-diones. Tetrahedron, 2016, 72, 4245-4251. https://doi.org/10.1016/j.tet.2016.05.059

26. Zhang, Z.;* Zheng, D.; Ma, N.; Bi, J. Br?nsted Acid-Promoted the Synthesis of Furo[2,3-b]quinolones. Chin. J. Org. Chem., 2017, 37, 1824-1829. https://doi.org/10.6023/cjoc201612032

27. Zhang, Z.;* Zhang, Y.; Huang, G.; Zhang, G.* Organoiodine reagent-promoted intermolecular oxidative amination: synthesis of cyclopropyl spirooxindoles. Org. Chem. Front., 2017, 4, 1372-1375. https://doi.org/10.1039/C7QO00156H

28. Zhang, Z.;* Huang, Y.; Huang, G.; Zhang, G.;* Liu, Q. [Bis-(trifluoroacetoxy)iodo]benzene-Mediated Oxidative Direct Amination C-N Bond Formation: Synthesis of 1H-Indazoles. J. Heterocyclic Chem., 2017, 54, 2426. https://doi.org/10.1002/jhet.2839/full

29. Zhang, Z.;* Gao, X.; Li, Z.; Zhang, G.;* Ma, N.; Liu, Q.; Liu, T. PIFA-Mediated oxidative cyclization of 1-aroyl-N-arylcyclopropane-1-carboxamides and their application in the synthesis of pyrrolo[3,2-c]quinolinones. Org. Chem. Front., 2017, 4, 404-408. https://doi.org/10.1039/C6QO00598E

30. Liu, Y.; Zhang, Z.;* Wan, Y.; Zhang, G.;* Li, Z.; Bi, J.; Ma, N.; Liu, T.; Liu, Q. Oxidation of beta-Ketoamides: The Synthesis of Vicinal Tricarbonyl Amides. J. Org. Chem., 2017, 82, 3901-3907 (Record by Organic Chemistry Portal. Please see: https://www.organic-chemistry.org/abstracts/lit5/816.shtm). https://doi.org/10.1021/acs.joc.6b03062

31. Yan, Y.; Zhang, Z.;* Wan, Y.; Zhang, G.;* Ma, N.; Liu, Q. Hypervalent Iodine(III)-Promoted Phenyl Transfer Reaction from Phenyl Hydrazides to Nitriles. J. Org. Chem., 2017, 82, 7957-7963. https://doi.org/10.1021/acs.joc.7b01215

32. Zhang, Z.;* Gao, X.; Wan, Y.; Huang, Y.; Huang, G.; Zhang, G.* Ammonium Acetate-Promoted One-Pot Tandem Aldol Condensation/Aza-Addition Reactions: Synthesis of 2,3,6,7-Tetrahydro-1H-pyrrolo[3,2-c]pyridin-4(5H)-ones. ACS Omega, 2017, 2, 6844-6851. https://doi.org/10.1021/acsomega.7b00626

33.  Zhang, Z.;* Gao, X.; Yu, H.; Bi, J.; Zhang, G.* Tandem Oxidative α-Hydroxylation/β-Acetalization Reaction of β-Ketoamides and Its Applications. ACS Omega, 2017, 2, 7746-7754. https://doi.org/10.1021/acsomega.7b01526


34.  Kai Sun*, Yunhe Lv, Zuodong Shi, Fangfang Fu, Chong Zhang, Zhiguo Zhang*, Direct Access to β-Selenosulfones at Room Temperature through Selenosulfonylation of Alkene, Sci. China Chem., 2017, 60, 730. https://link.springer.com/article/10.1007/s11426-016-0412-0?utm_source=xmol&utm_medium=affiliate&utm_content=meta&utm_campaign=DDCN_1_GL01_metadata

    35. Zhang, Z.;* Zheng, D.; Wan, Y.; Zhang, G.;* Bi, J.; Liu, Q.; Liu, T.; Shi, L. Selective Cleavage of Inert Aryl C-N Bonds in N-Aryl Amides. J. Org. Chem., 2018, 83, 1369-1376 (Record by Organic Chemistry Portal. Please see: https://www.organic-chemistry.org/abstracts/lit6/197.shtm,;該研究工作還被國際醫(yī)藥研發(fā)企業(yè)“藥明康德”公眾號——“實用有機合成化學(xué)”的“保護基的引入/消除”專欄收錄). https://doi.org/10.1021/acs.joc.7b02880

36. Hu, C.; Zhang, Z.;* Gao, W.; Zhang, G.;* Liu, T.; Liu, Q. PIFA-promoted intramolecular oxidative C(aryl)-H amidation reaction: Synthesis of quinolino[3,4-b]quinoxalin-6(5H)-ones. Tetrahedron, 2018, 74, 665-671. https://doi.org/10.1016/j.tet.2017.12.016

37. Wu, H.; Zhang, Z.;* Ma, N.; Liu, Q.; Liu, T.; Zhang, G.* Synthesis of Acridines from O-Aminoaryl Ketones and Arylboronic Acids by Copper Trifluoroacetate-Mediated Relay Reactions. J. Org. Chem., 2018, 83, 12880-12886 (Highlight by SYNFACTS, Synfacts, 2018, 14, 1230). https://doi.org/10.1021/acs.joc.8b01828


38. Zhang, Z.;* Gao, X.; Yu, H.; Zhang, G.;* Liu, J. Copper-Catalysed (Diacetoxyiodo)benzene-Promoted Aerobic Esterification Reaction: Synthesis of Oxamates from Acetoacetamides. Adv. Synth. Catal., 2018, 360, 3406-3411. https://doi.org/10.1002/adsc.201800616

39. Wu, H.; Zhang, Z.;* Liu, Q.; Liu, T.; Ma, N.; Zhang, G.* Syntheses of Acridones via Copper(II)-Mediated Relay Reactions from O-Aminoacetophenones and Arylboronic Acids. Org. Lett., 2018, 20, 2897-2901. https://doi.org/10.1021/acs.orglett.8b00957

40. Lu, N.; Zhang, Z.;* Ma, N.; Wu, C.; Zhang, G.;* Liu, Q.; Liu, T. Copper-Catalyzed Difunctionalization of Allenes with Sulfonyl Iodides Leading to (E)-α-Iodomethyl Vinylsulfones. Org. Lett., 2018, 20, 4318 (Record by Organic Chemistry Portal. Please see: https://www.organic-chemistry.org/abstracts/lit6/423.shtm). https://doi.org/10.1021/acs.orglett.8b01765

41. Wan, Y.; Zhang, Z.;* Ma, N.; Bi, J.; Zhang, G.* Acylamino-Directed Specific Sequential Difunctionalizations of Anilides via Metal-Free Relay Reactions for p-Oxygen and o-Nitrogen Incorporation. J. Org. Chem., 2018, 84, 780-791 (Record by Organic Chemistry Portal. Please see: https://www.organic-chemistry.org/Highlights/2019/14October.shtm). https://doi.org/10.1021/acs.joc.8b02636

42. Zhang, Z.;* Wang, S.; Hu, C.; Ma, N.; Zhang, G.;* Liu, Q. Copper(I)-catalyzed benzylic C(sp3)–H geminal difunctionalization: Successive oxidative intramolecular amidation and hydroxylation. Tetrahedron, 2018, 74, 7472-7479. https://doi.org/10.1016/j.tet.2018.11.023

43. Zhang, Z.;* Li, X.; Song, M.; Wan, Y.; Zheng, D.; Zhang, G.;* Chen, G.* Selective Removal of Aminoquinoline Auxiliary by IBX Oxidation. J. Org. Chem., 2019, 84, 12792-12799 (Highlight by SYNFACTS, Synfacts, 2019, 15, 1209). https://doi.org/10.1021/acs.joc.9b01362

44. Zhang, Z.;* Wang, S.; Zhang, Y.; Zhang, G.* Regiospecific Cleavage of S-N Bonds in Sulfonyl Azides: Sulfonyl Donors. J. Org. Chem., 2019, 84, 3919-3926 (Record by Organic Chemistry Portal. Please see: https://www.organic-chemistry.org/abstracts/lit6/766.shtm). https://doi.org/10.1021/acs.joc.8b03046

45. Zhang, Z.;* Li, X.; Li, Y.; Guo, Y.; Zhao, X.; Yan, Y.; Sun, K.; Zhang, G.* Iodine-mediated aryl transfer reaction from arylhydrazine hydrochlorides to nitriles. Tetrahedron, 2019, 75, 3628-3635. https://doi.org/10.1016/j.tet.2019.05.034



46. Kai Sun,* Songnan Wang, Ranran   Feng, Yixiao Zhang, Xin Wang, Zhiguo Zhang,* Bing Zhang, Copper-Catalyzed Radical Selenodifluoromethylation of Alkenes: Access to CF2-Containing γ-Lactams, Org. Lett., 2019, 21, 2052. ( ESI高被引論文) https://pubs.acs.org/doi/10.1021/acs.orglett.9b00240


47. Sun, K.; Li, G.; Li, Y.; Yu, J.; Zhao, Q.; Zhang, Z.;* Zhang, G.* Oxidative Radical Relay Functionalization for the Synthesis of Benzimidazo[2,1-a]iso-quinolin-6(5H)-ones. Adv. Synth. Catal., 2020, 362, 1947-1954. https://doi.org/10.1002/adsc.202000040


48. Song, M.; Zhang, Z.;* Zheng, D.; Li, X.; Liang, R.; Zhao, X. N.; Shi, L.; Zhang, G.* Hypervalent Organoiodine Promoted Dearylation Reaction of N-Aryl Sulfonamides. Chin. J. Org. Chem., 2020, 40, 2433-2441. https://doi.org/10.6023/cjoc202001007

49. Gao, W.; Wan, Y.; Zhang, Z.;* Wu, H.; Liu, T.; Zhang, G.* The Hofmann reaction involving annulation of o-(pyridin-2-yl)aryl amides selectively and rapidly leads to potential photocatalytically active 6H-pyrido[1,2-c]quinazolin-6-one derivatives. Green Chem., 2020, 22, 7955-7961. https://doi.org/10.1039/d0gc02777d


50. Zhang, Z.;* Song, X.; Li, G.; Li, X.; Zheng, D.; Zhao, X.; Miao, H.; Zhang, G.* Liu, L., Synthesis of polycyclic spiro-fused indolines via IBX-mediated cascade cyclization. Chin. Chem. Lett., 2021, 32, 1423–1426. https://doi.org/10.1016/j.cclet.2020.11.001

51. Wan, Y.; Wu, H.; Ma, N.; Zhao, J.; Zhang, Z.;* Gao, W.; Zhang, G.,* De novo design and synthesis of dipyridopurinone derivatives as visible-light photocatalysts in productive guanylation reactions. Chem. Sci., 2021, 12, 15988-15997. https://doi.org/10.1039/d1sc05294b



52. Xin Wang, Sa Guo, Yan Zhang, Zhiguo Zhang,* Guisheng Zhang,* Yong Ye, Kai Sun*, Metal-Free Organoselenium-Enabled Radical Relay Azidation–Carbocyclization, Adv. Synth. Catal., 2021, 363, 3290-3296. https://onlinelibrary.wiley.com/doi/10.1002/adsc.202100208


53. Sun, K.;* Li, G.; Guo, S.; Zhang, Z.;* Zhang, G.,* Copper-catalyzed radical cascade cyclization for synthesis of CF3-containing tetracyclic benzimidazo[2,1-a]iso-quinolin-6(5H)-ones. Org. Biomol. Chem., 2021, 19, 375-378. https://doi.org/10.1039/d0ob02210a



54. 張志國;* 曹夕陽; 王港; 方世亮; 吳昊; 張貴生, 呋喃[3,2-b]吲哚類化合物堿性條件下擴環(huán)重排反應(yīng). 河南師范大學(xué)學(xué)報,2022, 50, 95-101. https://doi.org/10.16366/j.cnki.1000-2367.2022.02.012

55. Zhang, Z.;* Cao, X. Y.; Wang, G.; Zhang, G.;* Zhang, X. J., Straightforward synthesis of biologically valuable nonsymmetrical malonamides under mild conditions. Green Chem. 2022, 24, 3035-3041. https://doi.org/10.1039/d2gc00395c

56. Wan, Y.; Liu, Q.; Wu, H.; Zhang, Z.;* Zhang, G.,* 2,11-Dimethoxyldipyridopurinone as an efficient reducing visible-light photocatalyst for organic transformations. Org. Chem. Front. 2022, 9, 1634-1641. https://doi.org/10.1039/D1QO01914G


57. Sa Guo, Xin Wang, Dongyang Zhao, Zhiguo Zhang, Guisheng Zhang, Shi Tang, Kai Sun*, Convenient Access to Ester-Containing Quinolinones Through Sequential Radical Alkoxycarbonylation Cyclization Hydrolysis Process, Asian J. Org. Chem., 2022, 11, e20210081. https://doi.org/10.1002/ajoc.202100812


58. Cao, X.; Zhang, Z.;* Li, J.; Shi, B.; Li, M.; Zhang, G.;* Zhang, X., Rh(III)-Catalyzed Oxidative Domino C-H/N-H Annulation: Diarylureas as Arylamine Donors for the Assembly of Indolo[2,1-a]isoquinolines. J. Org. Chem. 2022, 87, 13672-13682. https://doi.org/10.1021/acs.joc.2c01334


59. Zhang, Z.;* Cao, X.; Song, X.; Wang, G.; Shi, B.; Li, X.; Ma, N.; Liu, L.; Zhang, G.,* Metal-free nucleophilic 7,8-dearomatization of quinolines: Spiroannulation of aminoquinoline protected amino acids. Chin. Chem. Lett. 2023, 34, 107779. https://doi.org/10.1016/j.cclet.2022.107779

60. Zhang, G.;* Chen, L.; Hu, Z.; Zhang, Z.;* Bi, J.; Li, M.; Zhang, X., Organocatalytic Cloke–Wilson Rearrangement: Carbocation-Initiated Tandem Ring Opening/Cyclization of Cyclopropanes under Neutral Conditions. J. Org. Chem. 2023, 88, 1003-1017. https://doi.org/10.1021/acs.joc.2c02415

61.  Shi, B.; Zhang, Z.; Cao, X.; Ma, N.; Li, S.; Wu, H.; Zhang, X.; Zhang, G., Anion Cascade Reactions II: Synthesis of 3-Isoquinuclidone-Based Bridged Polycyclic Lactams. Org. Lett. 202325, 6846-6852. https://doi.org/10.1021/acs.orglett.3c02356


62.  Li, M.; Zhang, Z.;* Ma, N.; Zhao, J.; Wu, H.; Liu, Q.; Zhang, G.* Anion Cascade Reactions. Part I: Synthesis of 3-Isoquinuclidones from a Nazarov-like Reagent. Org. Lett. 202325, 6840-6845. https://doi.org/10.1021/acs.orglett.3c02355


63.  Li, M.; Li, J.; Zhang, Z.;* Chen, L.; Ma, N.; Liu, Q.; Zhang, X.; Zhang, G.* Palladium-catalyzed intramolecular aza-Wacker-type cyclization of vinyl cyclopropanecarboxamides to access conformationally restricted aza[3.1.0]bicycles. RSC Advances 2023, 13, 27158-27166. https://doi.org/10.3390/molecules28093691

    


64.  Li, J.; Zhang, Z.;* Chen, L.; Li, M.; Zhang, X.; Zhang, G.* Base-Promoted Intramolecular Addition of Vinyl Cyclopropanecarboxamides to Access Conformationally Restricted Aza[3.1.0]bicycles. Molecules 2023, 28, 3691. https://doi.org/10.1039/d3ra05440c



專利情況:

1. 張志國,,劉青鋒,,張貴生,田慶,,高選擇性地脫除2,6-二甲基-4-吡啶酮衍生物的α-單甲基的簡單,、有效的方法,ZL201210469746.8,,授權(quán)日期:2014.08.27,。

2. 張志國,劉青鋒,,張貴生,,田慶,2,6-二甲基-4-吡啶酮衍生物的2位和6位甲基的簡單,、有效的脫去方法,,ZL201210517552.0,授權(quán)日期:2014.08.27,。

3. 張志國,,鄭丹,麻娜娜,,張貴生,,劉青鋒,,一種合成呋喃[2,3-b]喹啉類化合物的方法,ZL201510195570.5,,授權(quán)日期:2020.04.28,。

4. 張志國,黃媛媛,,麻娜娜,,張貴生,劉青鋒,,一種合成4氫-吡咯[3,2-c]吡啶-4-酮類化合物的方法,,ZL201510195454.3,授權(quán)日期:2020.04.28,。

5. 張志國,,曹夕陽,張貴生,,一種聯(lián)烯類化合物雙磺?;姆椒ǎ琙L202110537926.4,,授權(quán)日期:2022.04.26,。

6. 張志國,胡兆康,,張貴生,,劉青鋒,一種合成2,,4-雙取代喹啉類化合物的新方法,,ZL02110613110.5,授權(quán)日期:2022.06.03,。

7. 張貴生,,劉青鋒,張志國,,具有抗癌活性的3'-疊氮基表阿霉素的合成,,ZL201110023054.6,授權(quán)日期:2014.06.25,。

8.  張志國,,高文婧,張貴生,,麻娜娜,,一種合成6-吡啶[1,2-c]喹唑啉-6-酮類化合物的新方法,ZL201811630556.3,授權(quán)日期:2022.09.13,。

9. 張志國,,曹夕陽,張貴生,,一種不對稱丙二酰胺類化合物及其合成方法,ZL202111615221.6,,授權(quán)日期:2023.09.22,。

10. 張志國,胡兆康,,張貴生,,劉青鋒,一種合成2,3-二氫呋喃類化合物的方法,,申請?zhí)枺?02111613650X,,授權(quán)日期:2023.01.17

11. 張志國,高文婧,,張貴生,,麻娜娜,一種合成吡啶[1’,2’:1,5]吡唑[3,4-b]喹喔啉類化合物的方法,,申請?zhí)枺?01811629925.7,,授權(quán)日期:2024.04.16。

12. 張貴生,,張志國,,麻娜娜,劉青鋒,,李忠聯(lián),,一種氧化1,3-二羰基化合物的亞甲基成酮的方法,申請?zhí)枺?01510214235.5,,申請日期:2015.04.10,。

13. 張貴生,張志國,,麻娜娜,,劉青鋒,張偉,,一種將2,3-二氫吡咯氧化成吡咯的方法,,申請?zhí)枺?01510195453.9,申請日期:2015.04.10,。

14. 張志國,,張貴生,閆嚴(yán),劉青鋒,,一種二級酰胺類化合物的合成方法,,申請?zhí)枺?01611135725.7,申請日期:2016.12.18,。

15. 張志國,,李祥,張貴生,,麻娜娜, 一種去除氨基上喹啉保護基的新方法,,申請?zhí)枺?01811514058.2,申請日期:2018.11.29,。



獲獎和榮譽:


1. 東北師范大學(xué),,研究生學(xué)術(shù)活動先進個人,2008年,。

2. 東北師范大學(xué),,優(yōu)秀研究生獎學(xué)金,2008年,。

3. 東北師范大學(xué),,優(yōu)秀研究生獎學(xué)金,2010年,。

4. 東北師范大學(xué),,研究生優(yōu)秀畢業(yè)生,2010年,。

5. 河南師范大學(xué),,優(yōu)秀教師,2011年,。

6. 吉林省優(yōu)秀博士學(xué)位論文,,吉林省學(xué)位委員會,2012年5月,。

7. 河南省優(yōu)秀博士后研究人員,,河南省人力資源和社會保障廳,2014,。

8. 河南師范大學(xué)“優(yōu)秀青年科研創(chuàng)新人才”,,2014年12月。

9. 河南省高校青年骨干教師,,河南省教育廳,,2014年。

10. 河南師范大學(xué)青年五四獎?wù)拢?016年5月,。

11. 河南省高??萍紕?chuàng)新人才支持計劃,,河南省教育廳,2017年,。

12. 河南省杰出青年科學(xué)基金,,2022年。

13. 河南省教育廳學(xué)術(shù)技術(shù)帶頭人,,2022年,。

14. 河南省教育廳科技成果獎一等 (2/12),2024年,。



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