鈕大文課題組成立于2015年8月,課題組依托四川大學(xué)華西醫(yī)院生物治療國家重點(diǎn)實(shí)驗(yàn)室、四川大學(xué)化學(xué)工程學(xué)院,面向國家新藥研發(fā)重大需求,聚焦糖化學(xué)前沿領(lǐng)域,開發(fā)用于糖類候選藥物合成的新反應(yīng)、新試劑以及新催化劑。
獨(dú)立工作以來,課題組已經(jīng)陸續(xù)在Nature(2024)、Science(2023)、Nature Chemistry(2022)、Nature Synthesis (2023)、Nature Catalysis (2020)、Acc.Chem.Rev.(2023)、Nature Communications(2022、2020)、JACS (2021、2019、2016)、Chem (2017)、Angewandte (2023、2023、2022、2021、2021、2020、2020、2018、2018、2017、2017)、Chemical Reviews (2018)等權(quán)威期刊上發(fā)表文章30余篇。此外,鈕大文教授在博士、博士后工作期間在Nature、Nature Chemistry、Nature Protocols、JACS、Angewandte等權(quán)威期刊發(fā)表文章10余篇。
鈕大文教授曾獲中國化學(xué)會(huì)青年化學(xué)獎(jiǎng)(2021), 惠永正糖科學(xué)獎(jiǎng)青年創(chuàng)新獎(jiǎng)(2023), 中國化學(xué)會(huì)糖化學(xué)青年學(xué)者獎(jiǎng)(2023), Thieme Chemistry Journals Award (2016),Reaxys PhD Prize (2014,全球每年三名Winners),國家優(yōu)秀自費(fèi)留學(xué)生獎(jiǎng)(2013)等獎(jiǎng)項(xiàng)。
【教育經(jīng)歷】
2014-2015 博士后 麻省理工學(xué)院(M.I.T.) 導(dǎo)師 Stephen L. Buchwald
2009-2013 博士 美國明尼蘇達(dá)大學(xué) 導(dǎo)師 Thomas R. Hoye
【研究方向】
課題組一直致力于開發(fā)新方法解決糖類化合物的合成問題,同時(shí)借鑒糖化學(xué)研究中所積累的知識(shí)以解決更基礎(chǔ)的合成化學(xué)難題。研究領(lǐng)域主要是針對(duì)糖化學(xué)中的位點(diǎn)選擇性、化學(xué)選擇性以及立體選擇性等問題開發(fā)新反應(yīng)方法學(xué),從而以高效、快捷、易操作的策略解決糖類化合物的合成難題。
主要研究內(nèi)容包括:
1)多羥基天然藥物以及糖類化合物的選擇性修飾
2)過渡金屬參與的糖類化合物的合成方法學(xué)研究
3)含糖化合物的藥物化學(xué)以及化學(xué)生物學(xué)研究
【招生方向】
研究生招生與博士后、副研究員招聘專業(yè)和方向:
化學(xué)、藥學(xué)、制藥工程、化學(xué)生物學(xué)、生物與醫(yī)藥等。詳情咨詢請(qǐng)聯(lián)系鈕教授 (niudawen@126.com)。
詳情請(qǐng)見課題組主頁:http://www.theniugroup.com/
【代表性論著】
發(fā)表文章 (獨(dú)立工作):
1. Dang, Q. D.; Deng, Y. H.; Sun, T. Y.; Zhang, Y.; Li, J.; Zhang, X.; Wu, Y. D.*; Niu, D.*, Catalytic Glycosylation for Minimally Protected Donors and Acceptors. Nature 2024,ASAP.
2. Deng, L. F.; Wang, Y.; Xu, S.; Shen, A.; Zhu, H.; Zhang, S.; Zhang, X.; Niu, D.*, Palladium catalysis enables cross-coupling-like S(N)2-glycosylation of phenols. Science 2023, 382 (6673), 928-935.
3. Zhang, C.; Zuo, H.; Lee, G. Y.; Zou, Y.; Dang, Q. D.; Houk, K. N.*; Niu, D.*, Halogen-bond-assisted radical activation of glycosyl donors enables mild and stereoconvergent 1,2-cis-glycosylation. Nature Chemistry 2022, 14, 686–694
4. Zhang, C.; Xu, S.-Y.; Zuo, H.; Zhang, X.; Dang, Q.-D.; Niu, D.*, Direct synthesis of unprotected aryl C-glycosides by photoredox Ni-catalysed cross-coupling. Nature Synthesis 2023, 2, 251-260
5. Ren-Zhe Li, Da-Qi Liu, Dawen Niu*. Asymmetric O-propargylation of secondary aliphatic alcohols. Nature Catalysis 2020, 3, 672–680.
6. Shang, W. D.; Niu, D.*, Radical Pathway Glycosylation Empowered by Bench-Stable Glycosyl Donors. Accounts Chem Res 2023, 56 (18), 2473-2488.
7. Zuo, H.; Zhang, C.; Zhang, Y.; Niu, D.*, Base-Promoted Glycosylation Allows Protecting Group-Free and Stereoselective
-Glycosylation of Carboxylic Acids. Angew Chem Int Edit 2023, 62 (42), e202309887.
8. Xu, S. Y.; Zhang, W.; Li, C. Y.; Li, Y. J.; Zeng, H. X.; Wang, Y. W.*; Zhang, Y.; Niu, D.*, Generation and Use of Glycosyl Radicals under Acidic Conditions: Glycosyl Sulfinates as Precursors. Angew Chem Int Edit 2023,e202218303.
9. Xie, D. M.; Wang, Y. W.; Zhang, X.*; Fu, Z. Y.; Niu, D.*, Alkyl/Glycosyl Sulfoxides as Radical Precursors and Their Use in the Synthesis of Pyridine Derivatives. Angew Chem Int Edit 2022, 61.
10. Pu, X.; Dang, Q. D.; Yang, L.; Zhang, X.*; Niu, D.*, Doubly stereoconvergent construction of vicinal all-carbon quaternary and tertiary stereocenters by Cu/Mg-catalyzed propargylic substitution. Nat Commun 2022, 13, 2457.
11. Wan, L. Q.; Zhang, X.; Zou, Y. K.; Shi, R.; Cao, J. G.; Xu, S. Y.; Deng, L. F.; Zhou, L.; Gong, Y. Q.; Shu, X. L.; Lee, G. Y.; Ren, H. Y.; Dai, L. Z.; Qi, S. Q.; Houk, K. N.; Niu, D.*, Nonenzymatic Stereoselective S-Glycosylation of Polypeptides and Proteins. J Am Chem Soc 2021, 143, 11919-11926.
12. Wang, Y., Deng, L., Zhang, X.*, Mou, Z., and Niu, D.*, A radical approach to make unnatural amino acids through converting C–S bonds in cysteine derivatives to C–C bonds. Angew. Chem. Int. Ed. 2021, 60, 2155–2159
13. Shang, W., Su, S.‐N., Shi, R., Mou, Z.‐D., Yu, G.‐Q., Zhang, X.* and Niu, D.*, Generation of Glycosyl Radicals from Glycosyl Sulfoxides and Its Use in the Synthesis of C‐linked Glycoconjugates. Angew. Chem. Int. Ed. 2021, 60, 385–390
14. Gong, L.; Sun, H. B.; Deng, L. F.; Zhang, X.; Liu, J.; Yang, S. Y.; Niu, D.*, Ni-Catalyzed Suzuki-Miyaura Cross-Coupling of alpha-Oxo-vinylsulfones To Prepare C-Aryl Glycals and Acyclic Vinyl Ethers. J Am Chem Soc 2019, 141 (19), 7680-7686.
15. Tang, S.; Zhang, X.; Sun, J.; Niu, D.*; Chruma, J. J.*, 2-Azaallyl Anions, 2-Azaallyl Cations, 2-Azaallyl Radicals, and Azomethine Ylides. Chem Rev 2018, 118 (20), 10393-10457.
16. Sun, H. B.; Gong, L.; Tian, Y. B.; Wu, J. G.; Zhang, X.; Liu, J.; Fu, Z.; Niu, D.*, Metal- and Base-Free Room-Temperature Amination of Organoboronic Acids with N-Alkyl Hydroxylamines. Angew Chem Int Ed Engl 2018, 57 (30), 9456-9460.
17. Shang, W.; Mou, Z. D.; Tang, H.; Zhang, X.; Liu, J.; Fu, Z.; Niu, D.*, Site-Selective O-Arylation of Glycosides. Angew Chem Int Ed Engl 2018, 57 (1), 314-318.
18. Fu, Z.; Deng, N.; Su, S. N.; Li, H.; Li, R. Z.; Zhang, X.*; Liu, J.; Niu, D.*, Diastereo- and Enantioselective Propargylation of 5H-Thiazol-4-ones and 5H-Oxazol-4-ones as Enabled by Cu/Zn and Cu/Ti Catalysis. Angew Chem Int Ed Engl 2018, 57 (46), 15217-15221.
19. Li, R. Z.; Tang, H.; Yang, K. R.; Wan, L. Q.; Zhang, X.; Liu, J.; Fu, Z.; Niu, D.*, Enantioselective Propargylation of Polyols and Desymmetrization of meso 1,2-Diols by Copper/Borinic Acid Dual Catalysis. Angew Chem Int Ed Engl 2017, 56 (25), 7213-7217.
20. Li, R.-Z.; Tang, H.; Wan, L.; Zhang, X.; Fu, Z.; Liu, J.; Yang, S.; Jia, D.; Niu, D.*, Site-Divergent Delivery of Terminal Propargyls to Carbohydrates by Synergistic Catalysis. Chem 2017, 3 (5), 834-845.
20. Liu, J.; Cao, C. G.; Sun, H. B.; Zhang, X.; Niu, D.*, Catalytic Asymmetric Umpolung Allylation of Imines. J Am Chem Soc 2016, 138 (40), 13103-13106.
發(fā)表文章 (Ph. D. 期間):
Niu, D.; Willoughby, P. H.; Baire, B.; Woods, B. P.; Hoye, T. R. Nature, 2013, 501, 531-534.
Niu, D.; Hoye, T. R. Nature Chemistry, 2014, 6, 34-40.
Niu, D.; Wang, T.; Woods, B. P.; Hoye, T. R. Org. Lett., 2014, 16, 254-257.
Niu, D.; Hoye, T. R. Org. Lett., 2012, 14, 828-831.
Willoughby, P. H.; Niu, D. (共一作); Wang, T.; Haj, M. K.; Hoye, T. R. J. Am. Chem. Soc., 2014, 136, 13657-13665.
Baire, B.; Niu, D. (共一作); Willoughby, P. H.; Woods, B. P.; Hoye, T. R. Nature Protocols, 2013, 8, 501-508.
Hoye, T. R.; Baire, B.; Niu, D.; Willoughby, P. H.; Woods, B. P. Nature, 2012, 490, 208-212.
發(fā)表文章 (Postdoc 期間):
Yang, Y.; Shi, S.; Niu, D; Liu, P.; Buchwald, S. L. Science, 2015, 349, 62-66.
Niu, D; Buchwald, S. L. J. Am. Chem. Soc., 2015, 137, 9716–9721.
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