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| 發(fā)布時(shí)間:2018-10-22 訪問(wèn)次數(shù):5787 作者:陳曉蓓 |

陳曉蓓 副教授、碩導(dǎo)
【聯(lián)系方式】 電話(huà):021-64253739 地址:華東理工大學(xué)徐匯校區(qū)實(shí)驗(yàn)十四樓西側(cè)403室 E-mail:xiaobei@ecust.edu.cn
【個(gè)人簡(jiǎn)歷】
本科畢業(yè)于復(fù)旦大學(xué)藥學(xué)院,獲藥學(xué)學(xué)士學(xué)位,隨后在中國(guó)科學(xué)院上海藥物研究所工作。之后赴美國(guó)新墨西哥大學(xué)化學(xué)系學(xué)習(xí),并獲博士學(xué)位。2015年5月加入華東理工大學(xué)藥學(xué)院,從事藥學(xué)相關(guān)教學(xué)和科研工作,先后主持教育部高校基本科研業(yè)務(wù)費(fèi)1項(xiàng)、國(guó)家自然科學(xué)基金青年基金1項(xiàng)和面上項(xiàng)目1項(xiàng),已在Nature Catalysis(Nature 子刊)、Organic Letters 、Chemical Communications等國(guó)際、國(guó)內(nèi)核心期刊上發(fā)表SCI論文10余篇。
【主要研究方向】
新穎實(shí)用的精準(zhǔn)氘代研究、開(kāi)發(fā)及其在藥物化學(xué)中的應(yīng)用
利用價(jià)廉易得的氘源,通過(guò)研究反應(yīng)機(jī)理,開(kāi)發(fā)新的化學(xué)活性和催化體系,來(lái)研發(fā)新穎實(shí)用的氘代反應(yīng),對(duì)化合物進(jìn)行精準(zhǔn)氘代,并將這些新型氘代方法應(yīng)用于藥物及天然產(chǎn)物的后期修飾中,以期改善藥物安全性及其藥代動(dòng)力學(xué)性質(zhì)等。 腫瘤免疫療法中小分子先導(dǎo)物的設(shè)計(jì)和研發(fā)
基于計(jì)算機(jī)輔助的藥物設(shè)計(jì)、合成和研發(fā)新型的小分子化合物,以尋找和發(fā)現(xiàn)具有較好抗腫瘤免疫療效的小分子候選藥物。 歡迎有志于藥物化學(xué)、藥物合成方法學(xué)以及新藥開(kāi)發(fā)領(lǐng)域研究的學(xué)生加入!! 招生專(zhuān)業(yè):學(xué)術(shù)碩士(藥學(xué));專(zhuān)業(yè)碩士(生物與醫(yī)藥(制藥工程))
【代表性論文發(fā)表】(2015年-至今)
Qian, P; Zhang, S*; Luo, F; Wang, J; Zhang, X; Liu, X; Chen, X; Wang, W*; Chen, X*; “Site-selective deuteration at the a-position of enals by an amine and bis(phenylsulfonyl)methane co-catalyzed H/D exchange reaction” Chem. Commun., 2022, 58, 11458-11461. Luo, F; Zhou, H; Chen, X*; Liu, X; Chen, X; Qian, P; Wu, X*; Wang, W*; Zhang, S*. “Synthesis of α‐Aryl Primary Amides from α‐Silyl Nitriles and Aryl Sulfoxides through [3,3]-Sigmatropic Rearrangement” Org. Lett., 2022, 24, 1700-1705. Gui, J; Cai, X; Chen, L; Zhou, Y; Zhu, W; Jiang, Y; Hu, M; Chen, X*; Hu, Y*; Zhang, S*. “Facile and practical hydrodehalogenations of organic halides enabled by calcium hydride and palladium chloride” Org. Chem. Front., 2021, 8, 4685-4692.
Chen, XB; Jiang, YR; Geng, HH; Liu, XY; Huang, YZ; Lu, JW; Gao, CJ; Zhang, SL*; Zhang, J*; Wang, W*. “Aldehydes Switch Regioselectivity: a Prins Cyclization Strategy for the Synthesis of Indoline-fused THFs and Indole-fused Oxepanes” Adv. Synth. Catal., 2020, 362, 13, 2620-2625. Geng, HH#; Chen, XB#*; Gui, JJ; Zhang, YT; Shen, ZY; Qian, PF; Chen, JW; Zhang, SL*; Wang, W*. “Practical synthesis of C1 deuterated aldehydes enabled by NHC catalysis” Nat. Catal., 2019, 2, 12, 1071-1077. Shen, ZY; Zhang, SL; Geng, HH; Wang, JR; Zhang, XY; Zhou, AQ; Yao, C; Chen, XB*; Wang, W*. “Trideuteromethylation Enabled by a Sulfoxonium Metathesis Reaction” Org. Lett., 2019, 21, 448-452. Qian, P; Wan, H; Jiang, J; Hu, Y; Chen, X;*Zhang S.-L.;*“Discovery of a Special Intramolecular Aldol-Like Reaction in the Synthesis of Related Substance E of Tadalafil” Chin. J. Org. Chem. 2016, 36, 1878-1882. Chen, X.; Zhang, Y.; Wan, H.; Wang, W.; Zhang, S.* “Stereoselective Organocatalytic Oxidation of Alcohols to Enals: A Homologation Method to Prepare Polyenes” Chem. Commun., 2016, 3532-3535. Chen, X.*; Fan, H.; Zhang, S.; Yu, C.; Wang, W.* “Facile Installation of 2-Reverse Prenyl Functionality into Indoles by A Tandem N-Alkylation-Aza-Cope Rearrangement Reaction and Its Application in Synthesis” Chem. Eur. J., 2016, 22, 716-723. Liu, S.; Chen, X. (共同一作); Hu, Y.; Yuan, L.; Chen, S.; Wu, P.; Wang, W.; Zhang, S.;* Zhang W. “An Efficient Method for the Production of Terminal Alkynes from 1,1-Dibromo-1-alkenes and its Application in the Total Synthesis of Natural Product Dihydroxerulin” Adv. Synth. Catal., 2015, 357, 553-560.
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