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                            <h2>孙旺盛</h2>
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                <p style="text-align:center"><img width="207" height="295" title="" style="width: 207px; height: 295px;" alt="" src="../../hdupf/img/202209/202209141663118671435954.jpg" border="0" vspace="0"/></p><p style="text-indent: 2em; text-align: left;"><span style="font-family: 宋体, SimSun;"></span></p><p style="text-indent:32px;line-height:27px"><span style="font-size:16px;font-family:&amp;#10">【基本情况】</span></p><p style="text-indent:32px;line-height:27px"><span style="font-size:16px;font-family:&amp;#10">孙旺盛，副教授，基础医学院/甘肃省新药临床前研究重点实验室，学术型硕士研究生导师。</span></p><p style="text-indent:32px;line-height:27px"><strong><span style="font-size:16px;font-family:黑体">【学习经历】</span></strong></p><p style="text-indent:32px;line-height:27px"><span style="font-size:16px;font-family:宋体">2005.09</span><span style="font-size:16px;font-family:宋体">—2009.06兰州大学生命科学学院生命科学技术基地班，学士</span></p><p style="text-indent:32px;line-height:27px"><span style="font-size:16px;font-family:宋体">2009.09</span><span style="font-size:16px;font-family:宋体">—2014.06兰州大学生命科学学院生物化学与分子生物学，博士</span></p><p style="text-indent:32px;line-height:27px"><strong><span style="font-size:16px;font-family:" tahoma="">【工作经历】</span></strong></p><p style="text-indent:32px;line-height:27px"><span style="font-size:16px;font-family:宋体">2014.07</span><span style="font-size:16px;font-family:宋体">—2017.05兰州大学</span><span style="font-size:16px;font-family:" tahoma="">基础医学院/甘肃省新药临床前研究重点实验室</span><span style="font-size:16px;font-family:宋体">，讲师</span></p><p style="text-indent:32px;line-height:27px"><span style="font-size:16px;font-family:宋体">2017.05</span><span style="font-size:16px;font-family:宋体">—至今兰州大学</span><span style="font-size:16px;font-family:" tahoma="">基础医学院/甘肃省新药临床前研究重点实验室</span><span style="font-size:16px;font-family:宋体">，副教授、硕士生导师</span></p><p style="text-indent:32px;line-height:27px"><strong><span style="font-size:16px;font-family:" tahoma="">【目前承担课程】</span></strong></p><p style="text-indent:32px;line-height:27px"><span style="font-size:16px;font-family:宋体;color:#333333;background:white">《创新创业教育》(本科生)</span></p><p style="text-indent:32px;line-height:27px"><span style="font-size:16px;font-family:宋体;color:#333333;background:white">《药物研发基本原理》（研究生）</span></p><p style="text-indent:32px;line-height:27px"><span style="font-size:16px;font-family:宋体;color:#333333;background:white">《多肽生化与多肽药化》（研究生）</span></p><p style="text-indent:32px;line-height:27px"><strong><span style="font-size:16px;font-family:" tahoma="">【主要科研成果】</span></strong></p><p style="text-indent:48px;line-height:27px"><strong><span style="font-size:16px;font-family:" tahoma="">研究方向：</span></strong><span style="font-size:16px;font-family:" tahoma="">多肽药物化学与药理学、创新多肽药物发现</span></p><p style="text-indent:48px;line-height:27px"><strong><span style="font-size:16px;font-family:" tahoma="">主持或参与科研项目：</span></strong></p><p style="text-indent:48px;line-height:27px"><span style="font-size:16px;font-family:宋体">1.</span><span style="font-size:16px;font-family:宋体">生物大分子药物设计、制备与智能递送关键技术研究，中国医学科学院医学与健康科技创新工程重大协同创新项目，项目号：2021-I2M-1-026，子课题负责人，子课题经费392万元，2021年10月-2025年12月</span></p><p style="text-indent:48px;line-height:27px"><span style="font-size:16px;font-family:宋体">2. </span><span style="font-size:16px;font-family:宋体">基于非天然氨基酸的多肽药物修饰及临床导向的多肽药物研发，中国医学科学院医学与健康科技创新工程，项目号：2021-I2M-3-001，参加，2021年10月-2025年12月</span></p><p style="text-indent:48px;line-height:27px"><span style="font-size:16px;font-family:宋体">3.</span><span style="font-size:16px;font-family:宋体">多肽药物的精准修饰方法，中国医学科学院医学与健康科技创新工程多肽研究创新单元，项目号：2019-I2M-5-074，参加，1500万元，2019年1月-2023年12月</span></p><p style="text-indent:48px;line-height:27px"><span style="font-size:16px;font-family:宋体">4.</span><span style="font-size:16px;font-family:宋体">基于脱氢丙氨酸残基的肽库构建策略及其在多肽抗生素发现中的应用, 兰州市科技局，项目号：2019-4-4, 第一参与人、项目联系人，25万元，2019年12月-2021年12月</span></p><p style="text-indent:48px;line-height:27px"><span style="font-size:16px;font-family:宋体">5. </span><span style="font-size:16px;font-family:宋体">噁唑酮参与的不对称环加成反应及其在生物活性氮杂环合成中的应用，国家自然科学基金青年科学基金，项目号：21502079，主持，21万元，2016年1月-2018年12月</span></p><p style="text-indent:48px;line-height:27px"><strong><span style="font-size:16px;font-family:" tahoma="">发表主要论文或专著:</span></strong><span style="font-size:16px;font-family:" tahoma="">10</span><span style="font-size:16px;font-family:" tahoma="">篇以内代表性成果即可，容易产生学术争议的论文尽量避免。</span></p><p style="margin-left:24px"><span style="font-size:15px">1.<span style="font:9px " new="" times="">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span></span><span style="font-size:15px">Y. Li, J. Li, G. Bao, C. Yu, Y. Liu, Z. He, P. Wang, W. Ma, J. Xie, <strong>Wangsheng Sun</strong>* and R. Wang*, NDTP Mediated Direct Rapid Amide and Peptide Synthesis without Epimerization. <em>Org. Lett.</em><strong>2022</strong>, <em>24</em>, 1169−1174.</span><span style="font-size:15px;font-family:&amp;#10">（封面文章，</span><span style="font-size:15px">IF = 6.005</span><span style="font-size:15px;font-family:仿宋_GB2312">）</span></p><p style="margin-left:24px"><span style="font-size:15px">2.<span style="font:9px " new="" times="">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span></span><span style="font-size:15px">G. Bao<sup>+</sup>, P. Wang<sup>+</sup>, G. Li<sup>+</sup>, C. Yu, Y. Li, Y. Liu, Z. He, T. Zhao, J. Rao, J. Xie, L. Hong, <strong>Wangsheng Sun</strong>* and R. Wang*, 1,3-Dipolar Cycloaddition between Dehydroalanines and C,N-Cyclic Azomethine Imines: Application to Late-Stage Peptide Modification. <em>Angew. Chem. Int. Ed.</em><strong>2021</strong>, <em>60</em>, 5331–5338</span><span style="font-size:15px;font-family:仿宋_GB2312">（</span><span style="font-size:&amp;#10">Hot Paper, IF = 15.336</span><span style="font-size:15px;font-family:仿宋_GB2312">）</span></p><p style="margin-left:24px"><span style="font-size:15px">3.<span style="font:9px " new="" times="">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span></span><span style="font-size:15px">X. Guo,<sup>†</sup> J. Rao,<sup>†</sup> T. Yan, B. Zhang, W. Yang, <strong>Wangsheng Sun</strong>* and J. Xie*, Feleucin-K3 Analogue with an α</span><span style="font-size:15px;font-family:" cambria="">‑</span><span style="font-size:15px">(4-Pentenyl)-Ala Substitution at the Key Site Has More Potent Antimicrobial and Antibiofilm Activities in Vitro and in Vivo. <em>ACS Infect. Dis.</em><strong>2021</strong>, <em>7</em>, 64−78.</span><span style="font-size:&#10;font-family:仿宋_GB2312">（</span><span style="font-size:15px">IF = 5.084</span><span style="font-size:15px;font-family:仿宋_GB2312">）</span></p><p style="margin-left:24px"><span style="font-size:15px">4.<span style="font:9px " new="" times="">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span></span><span style="font-size:15px">J. Yang, Z. Wang, Z. He, G. Li, L. Hong, <strong>Wangsheng Sun</strong>* and R. Wang*, Organocatalytic Enantioselective Synthesis of Tetrasubstituted α-Amino Allenoates by Dearomative γ-Addition of 2,3-DisubstitutedIndoles to β,γ-Alkynyl-α-imino Esters. <em>Angew. Chem. Int. Ed.</em><strong>2020</strong>, <em>59</em>, 642 –647.</span><span style="font-size:15px;font-family:仿宋_GB2312">（</span><span style="font-size:&amp;#10">IF = 15.336</span><span style="font-size:15px;font-family:仿宋_GB2312">）</span></p><p style="margin-left:24px"><span style="font-size:15px">5.<span style="font:9px " new="" times="">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span></span><span style="font-size:15px">M. Zhang<sup>+</sup>, C. Yu<sup>+</sup>, J. Xie<sup>+</sup>, X. Xun, <strong>Wangsheng Sun</strong>*, L. Hong* and R. Wang*, Phosphoric Acid Catalyzed Asymmetric [2+2] Cyclization/Penicillin-Penillonic Acid Rearrangement. <em>Angew. Chem. Int. Ed.</em><strong>2018</strong>, <em>57</em>, 4921-4925.</span><span style="font-size:15px;font-family:仿宋_GB2312">（</span><span style="font-size:&amp;#10">IF = 15.336</span><span style="font-size:15px;font-family:仿宋_GB2312">）</span></p><p style="margin-left:24px"><span style="font-size:15px">6.<span style="font:9px " new="" times="">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span></span><span style="font-size:15px">G. Zhu,<sup>†</sup> Y. Li,<sup>†</sup> G. Bao, <strong>Wangsheng Sun</strong>*, L. Huang, L. Hong* and R. Wang*, Catalytic Kinetic Resolution of Spiro-Epoxyoxindoles with 1</span><span style="font-size:15px;font-family:" cambria="">‑</span><span style="font-size:15px">Naphthols: Switchable Asymmetric Tandem Dearomatization/Oxa-Michael Reaction and Friedel</span><span style="font-size:15px">−</span><span style="font-size:15px">Crafts Alkylation of 1</span><span style="font-size:15px;font-family:&amp;#10">‑</span><span style="font-size:15px">Naphtholsat the C4 Position. <em>ACS Catal.</em><strong>2018</strong>, <em>8</em>, 1810−1816. </span><span style="font-size:15px;font-family:&amp;#10">（</span><span style="font-size:15px">IF = 13.084</span><span style="font-size:15px;font-family:仿宋_GB2312">）</span></p><p style="margin-left:24px"><span style="font-size:15px">7.<span style="font:9px " new="" times="">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span></span><span style="font-size:15px">Z. Zeng, X. Xun, L. Huang, J. Xu, G. Zhu, G. Li, <strong>Wangsheng Sun</strong>*, L. Hong* and R. Wang*, Catalyst-free Tandem Halogenation/semipinacolRearrangement of Allyl Alcohols with Sodium Halide in Water. <em>Green Chem.</em>, <strong>2018</strong>, <em>20</em>, 2477–2480.</span><span style="font-size:15px;font-family:&amp;#10">（</span><span style="font-size:15px">IF = 10.182</span><span style="font-size:15px;font-family:仿宋_GB2312">）</span></p><p style="margin-left:24px"><span style="font-size:15px">8.<span style="font:9px " new="" times="">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span></span><span style="font-size:15px">J. Yang, <strong>Wangsheng Sun</strong>*, Z. He, C. Yu, G. Bao, Y. Li, Y. Liu, L. Hong* and R. Wang*, Access to α,γ-DiaminoDiacid Derivatives via OrganocatalyticAsymmetric 1,4-Addition of Azlactones and Dehydroalanines. <em>Org. Lett.</em><strong>2018</strong>, <em>20</em>, 7080−7084.</span><span style="font-size:15px;font-family:仿宋_GB2312">（</span><span style="font-size:&amp;#10">IF = 6.005</span><span style="font-size:15px;font-family:仿宋_GB2312">）</span></p><p style="margin-left:24px"><span style="font-size:15px">9.<span style="font:9px " new="" times="">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span></span><span style="font-size:15px">G. Zhu<sup>+</sup>, G. Bao<sup>+</sup>, Y. Li, <strong>Wangsheng Sun</strong>*, J. Li, L. Hong* and R. Wang*, Efficient Catalytic Kinetic Resolution of Spiro-epoxyoxindoles with Concomitant Asymmetric Friedel–Crafts Alkylation of Indoles. <em>Angew. Chem. Int. Ed.</em><strong>2017</strong>, <em>56</em>, 5332 –5335.</span><span style="font-size:15px;font-family:&amp;#10">（</span><span style="font-size:15px">IF = 15.336</span><span style="font-size:15px;font-family:仿宋_GB2312">）</span></p><p style="margin-left:24px"><span style="font-size:15px">10.<span style="font:9px " new="" times="">&nbsp;&nbsp; </span></span><span style="font-size:15px">B. Zhang, Y. Li, G. Bao, G. Zhu, J. Li, J. Wang, B. Zhang, <strong>Wangsheng Sun</strong>*, L. Hong* and R. Wang*, Regio- and StereoselectiveRing-opening Reaction of Spiro-epoxyoxindoles with Ammonia under Catalyst-free Conditions. <em>Green Chem.</em>, <strong>2017</strong>, <em>19</em>, 2107–2110.</span><span style="font-size:15px;font-family:仿宋_GB2312">（</span><span style="font-size:&amp;#10">IF = 10.182</span><span style="font-size:15px;font-family:仿宋_GB2312">）</span></p><p style="text-indent:32px;line-height:27px"><strong><span style="font-size:16px;font-family:" tahoma="">【社会兼职和社会服务】</span></strong></p><p style="text-indent:32px;line-height:27px"><span style="font-size:16px;font-family:&amp;#10">中国药理学会会员、甘肃省药学会会员、教育部学位论文评审专家、多个国际知名期刊<a name="_GoBack"></a>审稿专家。</span></p><p style="text-indent:32px;line-height:27px"><strong><span style="font-size:16px;font-family:" tahoma="">【获奖情况】</span></strong></p><p style="text-indent:32px;line-height:27px"><span style="font-size:16px;font-family:&amp;#10">教育部自然科学一等奖（排名12/15，2014）,甘肃省“优秀药学工作者”（2019）</span></p><p style="text-indent:32px;line-height:27px"><strong><span style="font-size:16px;font-family:" tahoma="">【联系方式】</span></strong></p><p style="text-indent:48px;line-height:27px"><span style="font-size:16px;font-family:" tahoma="">E-mail</span><span style="font-size:16px;font-family:" tahoma="">：sunws@lzu.edu.cn</span></p><p style="text-align: left; text-indent: 2em;"><span style="font-family: 宋体, SimSun;"></span><br/></p>            </div>
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