2018年江西师范大学孙建松课题组考研调剂信息:有机化学、药物化学方向
招生人数:2招生简介江西师范大学国家单糖化学合成工程技术研究中心孙建松课题组招收2018年调剂硕士研究生!!!一、调剂条件:1.优秀全日制本科毕
招生人数:2
招生简介
江西师范大学国家单糖化学合成工程技术研究中心孙建松课题组招收2018年调剂硕士研究生!!!
一、调剂条件: 1.优秀全日制本科毕业生; 2.分数能达到国家A类线;3.一志愿报考专业为相关专业(有机化学、药物化学(有机专业背景))。
二、需调剂生2-3名
三、招生简述: 课题研究方向是糖缀合物有机合成及糖苷化方法研究,招收真心喜欢有机化学的学生,务必吃苦耐劳,努力肯干,拥有梦想。老师待人真诚,在学术上严谨认真。实验中出现问题老师都会耐心帮忙解决,找方法。如果你这次考研失利了,那不要气馁,老师将会帮助你弥补遗憾!若有意向,请联系我们详谈,非诚勿扰!!! 邮件应包括以下材料:
1.个人简介
2.学业背景,是否应届
3. 科研经历,简明扼要即可
4.考研成绩单(各科成绩,报考院校及专业)
5.英语成绩证明(四六级成绩单的照片即可)
6.本科期间所修大部分主干专业课(主要是了解一下修过什么课程)
7.电子版证件照
8.联系方式(电话及qq)
四、招生联系人:孙建松教授 邮箱:jssun@jxnu.edu.cn
刘雷师兄电话 :*********** 邮箱 :***********@163.com QQ :393679334
五、导师信息:
孙建松,江西师范大学特聘教授,博士生导师。主要从事复杂天然糖缀合物及新型糖苷化方法的研究。师从中科院上海有机所俞飚教授、大连化物所韩秀文教授,先后完成了四个活性天然产物的首次全合成。2006在德国洪堡奖学金的资助下赴德国Konstanz大学世界著名糖化学家R. R. Schmidt课题组进行博后研究。2007年12月到中国科学院上海有机化学研究所工作,继续从事活性天然糖缀合物及新型糖苷化方法的研究。2014年10月加盟江西师范大学国家糖工程中心。先后在JACS, Angew. Chem. Int. Ed, Org. Lett, Acc. Chem. Res.等杂志上发表论文30余篇。
六、官网主页 http://www.escience.cn/people/sunjiansong/groupmember.html
七、研究课题:
1、江西省杰出人才资助计划:(20171BCB23036), 15万元,主持;
2、基金委地区基金:甜菊糖苷的高效合成研究(21762024),38万元,2018-2021,主持;
3、江西省自然科学重大项目:具有抗肿瘤活性的木质素糖苷合成研究(20161ACB20005),30万元,2016-2019,主持;
4、江西师范大学高层次人才引进启动经费:200万,2014-2018,主持;
5、国家自然科学基金面上项目:复杂核苷类抗生素 ampurimycin 及 miharamycin的合成研究(21372252) 80万,2014.1-2017.12,主持;
6、国家自然科学基金面上项目:复杂活性黄酮苷的合成研究(21572081)78万,2016-2019,主持;
八、代表论文:
1.Amipurimycin, total synthesis of the proposed structures and diastereoisomersShengyang Wang, Jiansong Sun, Qingju Zhang, Xin Cao, Yachen Zhao, Gongli Tang, & Biao Yu. Angew. Chem. Int. Ed.:2018 ,57 ,XXX-XXX
2.Highly Efficient Synthesis of Bioactive Oleanane-type SaponinsJing-Jing Sui, Wen-Hui Zhou, De-Yong Liu, Ming-Qing Li, Jian-Song Sun. Carbohydrate Research: 2017 ,452 ,43-46
3.o(pMethoxyphenylethynyl)phenyl Glycosides: Versatile NewGlycosylation Donors for the Highly Efficient Construction ofGlycosidic LinkagesYang Hu, Ke Yu, Li-Li Shi, Lei Liu, Jing-Jing Sui, De-Yong Liu, Bin Xiong, and Jian-Song Sun*. J. Am. Chem. Soc.: 2017,139 ,12736-12744
4.Synthetic Investigation toward the D-Ring-FunctionalizedCytotoxic Oleanane-Type Saponins Pithedulosides D and EShi-Jie Ge, Yuan-Hong Tu, Jian-Hui Xia, and Jian-Song Sun*. Eur. J. Org. Chem.: 2017 ,3929-3934
5.First Total Synthesis of the Bioactive Arylnaphthyl Lignan 4-O-Glycosides Phyllanthusmin D and 4-O-Acetylmananthoside BLei Liu, Yang Hu, Hui Liu, De-Yong Liu, Jian-Hui Xia, and Jian-Song Sun. Eur. J. Org. Chem.: 2017 ,3674-3680
6.The Catalytically Lignan-Activation-Based Approach for the Synthesis of (epi)Podophyllotoxin DerivativesJun-Hao Wan, Yang Hu, Hui Liu, Yuan-Hong Tu, Zhong-Yi He, Jian-Song Sun. J. Org. Chem.: 2017 ,82 ,5652-5662
7.Synthetic Access Toward Cycloastragenol GlycosidesTing Liu, Jin-Xi Liao, Yang Hu, Yuan-Hong Tu and Jian-Song Sun. J. Org. Chem.: 2017 ,82 ,4170-4178
8.The Antitumor Activity Study of Ginsenoside and Metabolites in Lung Cancer CellFeng-Yuan Xu, Wen-Qing Shang, Jia-Jun Yu, Qian Sun, Ming-Qing Li, Jian-Song Sun. Am. J. Transl. Res.: 2016 ,8 (4),1708-1718
9.Synthetic Investigation toward Apigenin 5-O-glycoside as well as Chemical Structure RevisionYang Hu, Yuan-Hong Tu, De-Yong Liu, Jin-Xi Liao, Jian-Song Sun. Org. Biomol. Chem.: 2016 ,14 ,4842-4847
10.A Higly Efficient Approach to Construct (epi)-podophyllotoxin 4-O-glycosidic Linkages as well as Its Application in Concise Synheses of Etoposide and TeniposideHui Liu, Jin-Xi Liao, Yuan-Hong Tu, Jian-Song Sun. Org. Lett.: 2016 ,18 ,1294-1297
11.Highly efficient synthesis of flavonol 5-O-glycosides with glycosyl ortho-alkynylbenzoates as donorsJin-Xi Liao, Nai-Li Fan, Hui Liu, Yuan-Hong Tu and Jian-Song Sun*. Organic & Biomolecular Chemistry: 2016 ,14 ,1221-1225
12.The chemical synthesis of aryltetralin glycosidesJian-Song Sun,* Hui Liu, Xiao-Hong Guo and Jin-Xi Liao. Organic & Biomolecular Chemistry: 2016 ,14 ,1188-1200
13.An Efficient Route to 2-Amino-β-galactosides and –glucosides via Stereoselective Michael-type Addition of 2-NitroglycalsWeihua Xue, Jiansong Sun*, Biao, Yu*. J. Org. Chem.: 2009 ,74 ,5079
14.An Efficient Approach to the Synthesis of Nucleosides, Gold(I)-Catalyzed N-Glycosylation of Pyrimidines and Purines with Glycosyl ortho-AlkynylbenzoatesQingju Zhang, Jiansong Sun*, Yugen Zhu, Fuyi Zhang, Biao Yu*. Angew. Chem. Int. Ed.: 2011 ,50 ,4933
15.Efficient Synthesis of Lupane-type Saponins via Gold(I)-Catalyzed Glycosylation with Glycosyl ortho-Alkynylbenzoates as DonorsYan Li, Jiansong Sun*, Biao Yu*. Org. Lett.: 2011 ,13 ,5508
16.Assembly of Naturally Occurring Golycosides, Evolved Tactics, and Glycosylation MethodsBiao Yu*, Jiansong Sun, Xiaoyu Yang. Acc. Chem. Res.: 2012 ,45 ,1227-1236
17.Construction of Interglycosidic N-O Lingkage via Direct Glycosylation of Sugar OximesJun Yu, Jiansong Sun*, Biao Yu*. Org. Lett.: 2012 ,14 ,4022-4025
18.Synthetic access toward the diverse ginsenosidesJun Yu, Jiansong Sun*,Yiming Niu, Rongyao Li, Jinxi Liao, Fuyi Zhang, Biao Yu*. Chem. Sci.: 2013 ,4 ,3899-3905
19. Jun Yu, Jiansong Sun*,Yiming Niu, Rongyao Li, Jinxi Liao, Fuyi Zhang, Biao Yu* Synthetic access toward the diverse ginsenosides, Chem. Sci. 2013, 4, 3899-3905.
20. Jun Yu, Jiansong Sun*, Biao Yu* Construction of Interglycosidic N-O Lingkage via Direct Glycosylation of Sugar Oximes. Org. Lett. 2012, 14, 4022-4025.
21. Biao Yu*, Jiansong Sun, Xiaoyu Yang Assembly of Naturally Occurring Golycosides, Evolved Tactics, and Glycosylation Methods. Acc. Chem. Res. 2012, 45, 1227-1236.
22. Yan Li, Jiansong Sun*, Biao Yu* Efficient Synthesis of Lupane-type Saponins via Gold(I)-Catalyzed Glycosylation with Glycosyl ortho-Alkynylbenzoates as Donors.
Org. Lett. 2011, 13, 5508.
23. Qingju Zhang, Jiansong Sun*, Yugen Zhu, Fuyi Zhang, Biao Yu*. An Efficient Approach to the Synthesis of Nucleosides, Gold(I)-Catalyzed N-Glycosylation of Pyrimidines and Purines with Glycosyl ortho-Alkynylbenzoates. Angew. Chem. Int. Ed. 2011, 50, 4933.
24. Weihua Xue, Jiansong Sun*, Biao, Yu*. An Efficient Route to 2-Amino-β-galactosides and –glucosides via Stereoselective Michael-type Addition of 2-Nitroglycals. J. Org. Chem. 2009, 74, 5079.
25. Jiansong Sun, Xiuwen Han, Biao Yu*. First Total Synthesis of Anemoclemoside B. Org. Lett.. 2005, 7, 1935,
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