化学所分子识别与功能实验室
学术带头人

       叶松  研究员

       

        国家杰出青年基金获得者

        电话:86-10-62641156;

        传真:86-10-62554449

        邮箱:songye@iccas.ac.cn

        课题组主页:http://songye.iccas.ac.cn/

     

    学术经历

    1991.9-1995.7   华东师范大学 学士

    1997.9-2002.7   中国科学院上海有机化学研究所 博士

    2002.9-2005.7   美国国家卫生研究院 博士后

    2005.7-至今       中国科学院化学研究所 研究员

     

    奖励与荣誉

    2002   中国科学院院长特别奖

    2004   全国百篇优秀博士学位论文

    2012   Thieme Chemistry Journals Award

    2012   国家自然科学二等奖(第三完成人)

    2014   国家杰出青年基金

     

    研究方向

    合成反应是有机合成化学的重要基础,课题组致力于高效、高选择性有机合成方法的发现与应用,发展不对称催化反应,实现重要有机分子骨架的高效快速构建。具体研究方向包括:

    1. 氮杂环卡宾催化

    2. 光催化协同催化

    3. 串联反应

    4. 杂环化合物合成

     

    Selected Work

    1. N-Heterocyclic carbene (NHC) catalyzed cross-coupling of homoenolate and enolate

     

    2. NHC-catalyzed [3+4] annualtions

     

    3. NHC-catalyzed Synthesis of multisubstituted benzenes

     

    Selected Publications

    1. Chen, X.-Y.; Chen, K.-Q.; Sun, D.-Q.;* Ye, S.* N-Heterocyclic carbene-catalyzed oxidative [3 + 2] annulation of dioxindoles and enals: cross coupling of homoenolate and enolate Chem. Sci., 2017, 8, 1936.

    2. Zhang, Z.-F.; Chen, K.-Q.; Zhang, C.-L.; Ye, S.* N-heterocyclic carbene-catalyzed synthesis of spirocyclopentene-oxindoles from bromoenals Chem. Commun., 2017, 53, 4327.

    3. Yi, L.; Zhang, Y.; Zhang, Z.-F.; Sun, D.-Q.;* Ye, S.* Synthesis of Dihydropyridinone-Fused Indoles and α‑Carbolines via N‑Heterocyclic Carbene-Catalyzed [3+3] Annulation of Indolin-2-imines and Bromoenals Org. Lett. 2017, 19, 2286.

    4. Zhang, C.-L.; Gao, Z.-H.; Liang, Z.-Q.; Ye, S.* N-Heterocyclic Carbene-Catalyzed Synthesis of Multi-Substituted Benzenes from Enals and α-Cyano-β-methylenones Adv. Synth. Catal. 2016, 358, 2862.

    5. Zhang, C.-L.; Ye, S.* N‑Heterocyclic Carbene-Catalyzed Construction of 1,3,5-Trisubstituted Benzenes from Bromoenals and α‑Cyano-β-methylenones Org. Lett. 2016, 18, 6408.

    6. Liang, Z.-Q.; Gao, Z.-H.; Jia W.-Q.; Ye, S.* “Bifunctional N-Heterocyclic Carbene Catalyzed [3+4] Annulation of Enals and Aurones” Chem. Eur. J. 2015, 21, 1868.

    7. Chen, X.-Y.; Gao, Z.-H.; Song, C.-Y.; Zhang, C.-L. Wang, Z.-X.;* Ye, S.* “N-Heterocyclic Carbene Catalyzed Cyclocondensation of α,β-Unsaturated Carboxylic Acids: Enantioselective Synthesis of Pyrrolidinone and Dihydropyridinone Derivatives” Angew. Chem. Int. Ed. 2014, 53, 11611.

    8. Chen, X.-Y.; Xia, F.; Cheng, J.-T.; Ye, S.* “Highly Enantioselective γ-Amination by N-Heterocyclic Carbene Catalyzed [4+2] Annulation of Oxidized Enals and Azodicarboxylates” Angew. Chem. Int. Ed. 2013, 52, 10644.

    9. Lv, H.; Jia, W.-Q.; Sun, L.-H.; Ye, S.* “N-Heterocyclic carbene catalyzed [4+3] annulation of enals and o-quinone methides: highly enantioselective synthesis of benzo-ɛ-lactones A” Angew. Chem. Int. Ed. 2013, 52, 8607.

    10. Shen, L.-T.; Jia, W.-Q.; Ye, S.* “Catalytic [4+2] Cyclization of α,β-Unsaturated Acyl Chlorides with 3-Alkylenyloxindoles: Highly Diastereo- and Enantioselective Synthesis of Spirocarbocyclic Oxindoles” Angew. Chem. Int. Ed. 2013, 52, 585.

    11. Shen, L.-T.; Sun, L.-H.; Ye, S.* “Highly enantioselective γ-amination of α,β-unsaturated acyl chlorides with azodicarboxylates: Efficient synthesis of chiral γ-amino acid derivatives” J. Am. Chem. Soc. 2011, 133, 15894.

    12. Shao, P.-L.; Chen, X.-Y.; Ye, S.* “Formal [3+2] cycloaddition of ketenes and oxaziridines catalyzed by chiral Lewis bases: Enantioselective synthesis of oxazolin-4-ones” Angew. Chem. Int. Ed. 2010, 49, 8412.

    13. Huang, X.-L.; He, L.; Shao, P.-L.; Ye, S.* “[4+2] Cycloaddition of ketenes with N-benzoyldiazenes catalyzed by N-heterocyclic carbenes” Angew. Chem. Int. Ed. 2009, 48, 192.

    14. Zhang, Y.-R.; He, L.; Wu, X.; Shao, P.-L.; Ye, S.* “Chiral N-heterocyclic carbene catalyzed staudinger reaction of ketenes with imines: Highly enantioselective synthesis of N-Boc β-Lactams” Org. Lett. 2008, 10, 277.

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