Zhangjianbo

 

Reviewer of New Drugs for China Food and Drug Administration;

Complex Carbohydrates Specialty Committee member;Chinese Society of Biochemistry and Molecular Biology

Molecular Biotechnique Specialty Committee member;Chinese Society of Biochemistry and Molecular Biology

Glycotechnology Specialty Committee member;Chinese Society of Biotechnology

Marine Drugs Specialty Committee member；Shanghai Pharmaceutical Association .

 

 

Glycochemistry and Glycobiology

Green Organic Syntheses

Carbohydrate Drugs

Biosurfactant

 

 

^{Academic Papers:}

 

^{43. Nianping Liu, Qingbing Wang, Xiangguang Tian, Yongda Zhou, Yijun Gu, Jianbo Zhang and Jie Tang, Synthesis of para-nitrophenyl--L-rhamnoside by two-step reaction, J. Carbohydrate Chem.. 2017, 36(4-6), 220-234;}

 

^{42. Saifeng Qiu, Guosheng Sun, Zekun Ding, Heshan Chen, Jianbo Zhang Ferric Chloride: An Eco-friendly Catalyst for the Stereoselective Synthesis of 2-Deoxy Aryl-O-Rhamnosides SYNLETT, 2017, 28, 2024-2029;}

 

^{41.Guosheng Sun, Saifeng Qiu, ZeKun Ding, HeShan Chen, JiaFen Zhou, ZhongFuWang, JianBo Zhang}

^{Magneticcore-shell Fe3O4@C-SO3H as an efficientand renewable “green catalyst” for the synthesis ofO-2, 3-unsaturatedglycopyranosides}

^{Synlett, 2017, 28, 347-352.}

 

^{40. Chen Heshan, Luo Xiaosheng, Qiu Saifeng, Sun Wengjie, Zhang Jianbo}

^{TMSOTfmediated stereoselective synthesis of alpha-C-glycosides from unactivated arylacetylenes.}

^{Glycoconj.J., 2017, 34, 13-20.}

 

^{39. Zhang Wan, Luo Xiaosheng, Wang Zhongfu, Zhang, Jianbo}

^{One-pot synthesis of beta-2, 6-dideoxyglycosides via glycosyl iodide intermediates}

^{J. Carbohydr. Chem., 2016, 35, 315-325.}

 

^{38. Zhou Jiafen, Chen Heshan, Shan, Junjie, Li, Juan, Yang Guofang, Chen Xuan,Xin Kunyun, Zhang Jianbo,Tang Jie}

^{FeCl3center dot 6H(2)O/C: An Efficient andRecyclable Catalyst for the Synthesis of 2, 3-Unsaturated O- and S-Glycosides}

^{J. Carbohydr. Chem., 2014, 33, 313-325.}

 

^{37.ZhangJianbo, Zhang Bo, Zhou Jiafen, Chen Heshan, Li Juan, Yang Guofang,Wang Zhongfu, Tang Jie}

^{A Facile H2SO4-SiO2-CatalyzedFerrier Rearrangement of 3, 4, 6-Tri-O-benzyl-D-glucal}

^{J. Carbohydr. Chem., 2013, 32, 380~391.}

 

^{36.Zhou Jiafen, Zhang Bo, Yang Guofang, Chen, Xuan,Wang Qingbing, Wang Zhongfu, Zhang Jianbo, Tang Jie}

^{A Facile H2SO4/4 angstrom MolecularSieves Catalyzed Synthesis of 2, 3 Unsaturated O-Glycosides via Ferrier-TypeRearrangement}

^{Synlett., 2010, 6, 893-96.}

 

^{35.Qiu Saifeng, Zhang Wan, Sun Guosheng, Wang Zhongfu, Zhang Jianbo}

^{A Facile and Direct Glycosidation Method for the Synthesis of 2-Deoxy a-Rhamnosides Catalyzed by Ferric Chloride}

^{ChemistrySelect, 2016, 4840-4844}

 

^{34.Chen Heshan, Xian Ting, Zhang Wan, Si Wenshuai, Luo Xiaosheng, Zhang Bo,Zhang Meiyu, Wang Zhongfu, Zhang Jianbo}

^{Anefficient method for the synthesis of pyranoid glycals}

^{Carbohydr.Res., 2016, 431, 42-46}

 

^{33.Zhang Jianbo, Fu Jie, Si Wenshuai, Wang Xiaohu, Wang Zhongfu, Tang Jie}

^{Ahighly efficient deprotection of the 2, 2, 2-trichloroethyl group at theanomeric oxygen of carbohydrates}

^{Carbohydr.Res., 2011, 346, 2290-2293}

 

^{32.Zhou JiaFen, Chen Xuan, Wang QingBing, Zhang Bo, Li Yan, Yusulf Abdullah,Wang ZhongFu, Zhang JianBo,Tang Jie}

^{H2SO4-SiO2:Highlyefficient and novel catalyst for the Ferrier-type glycosylation}

^{Chin.Chem. Lett., 2010, 21, 922-926}

 

^{31.Zhang Jianbo, Zhang Bo, Zhou Jiafen, LiJuan, Shi Chunjuan, Huang Ting, Wang Zhongfu, Tang Jie}

^{H2SO4-SiO2: HighlyEfficientandReusable Catalyst for per-O-Acetylation of Carbohydrates Under Solvent-FreeConditions}

^{J. Carbohydr. Chem., 2011, 30, 165-177}

 

^{30.Zhang Jianbo, Fu Jie, Chen Xuan, Gu Yijun, Tang Jie}

^{4-Nitrophenyl alpha-L-rhamnopyranoside hemihydrate}

^{Acta Crystallogr. Sect. E: Struct. Rep. Online, 2008, 64, O714~U1412}

 

^{29.Chen Li, Shi Chunjuan, Wang Xiaohu, ZhangBo, Zhang Jianbo, Tang Jie}

^{Vinyl acetate and sodium carbonate as a fastand efficient catalyst for per-O-acetylation of monosaccharides}

^{J. Chem. Res., 2008, 7, 380-382}

 

^{28.Wang Qingbing, Fu Jie, Zhang Jianbo}

^{A facile preparation of peracylatedalpha-aldopyranosyl chlorides with thionyl chloride and tintetrachloride}

^{Carbohydr. Res., 2008, 34, 2989-2991}

 

^{27.Shi Chunjuan, Zhang Jianbo, Fu Jie, TangJie}

^{Convenient per-O-acetylation of monosaccharides with vinyl acetate/Na3PO4-H2O}

^{Lett. Org. Chem., 2006, 3, 932-935}

 

^{26.Yang Guofang, Wang Qingbing, LuoXiaosheng, Zhang Jianbo, Tang Jie}

^{Facile TMSOTf-catalyzed preparationof 2-deoxy alpha-O-aryl-D-glycosides from glycosyl acetates}

^{Glycoconj. J., 2012, 29, 453-456}

 

^{25. Yu Luo‚ Yuhua Mei‚Jianbo Zhang‚Wei Luand Jie Tang“A concise synthesis of nornitidine via nickel- or palladium-catalyzed annulation”Tetrahedron 2006‚62‚9131-9134;}

 

^{24. Hai Yu‚ Harshal Chokhawala‚ Rebekah Karpel‚ Hui Yu‚ Bingyuan Wu‚ Jianbo Zhang et al‚ A Multifunctional Pasteurella multocida Sialyltransferase: A Powerful Tool for the Synthesis of Sialoside Libraries. J. Am. Chem. Soc. 2005‚ 127(50)‚ 17618-17619;}

 

^{23. Jianbo Zhang‚ Bingyuan Wu‚ Yingxin Zhang‚ Przemyslaw Kowal and Peng George Wang‚ “Creatine phosphate – creatine kinase in enzymatic synthesis of glycoconjugates.” Org. Lett.” 2003‚ 5‚ 2583-2586;}

 

^{22. Jianbo Zhang‚ Przemysław Kowal‚ Xi Chen and Peng George Wang‚ “Large-scale synthesis of globotriose derivatives through recombinant E. coli.” Org. Biomol. Chem. 2003‚ 1‚ 3048-3053;}

 

^{21. Jun Shao‚ Jianbo Zhang‚ Przemek Kowal‚ Yuquan Lu and Peng George Wang‚ “Efficient synthesis of globoside and isogloboside tetrasaccharides by using b(1→3) N-acetylgalactosaminyltransferase / UDP-N-acetylglucosamine C4 epimerase fusion protein” Chem. Commun. 2003‚ (12)‚ 1422-23.}

 

^{20. Ziye Liu‚ Yuquan Lu‚ Jianbo Zhang‚ Keith Pardee and Peng George Wang‚ “P1 trisaccharide (Gala1‚4Galb1‚4GlcNAc) synthesis by enzyme glycosylation reactions using recombinant Escherichia coli.” Appl. Environ. Microbiol. 2003‚ 69 (4)‚ 2110-5;}

 

^{19. Jun Shao‚ Jianbo Zhang‚ Przemek Kowal and Peng George Wang‚ “Donor substrate regeneration for efficient synthesis of globotetraose and isoglobotetraose.” Appl. Environ. Microbiol. 2002‚ 68 (11)‚ 5634-40;}

 

^{18. Jun Shao‚ Jianbo Zhang‚ Jozef Nahálkab and Peng George Wang‚“Biocatalytic synthesis of uridine 5’-diphosphate N-acetylglucosamine by multiple enzymes co-immobilized on agarose beads.” Chem. Comm. 2002‚ 2586-2587.}

 

^{17. Jun Shao‚ Jianbo Zhang‚ Przemek Kowal‚ Yuquan Lu and Peng George Wang‚“Overexpression and biochemical characterization of b-1‚ 3-N-acetylgalactosaminyl-transferase LgtD from Haemophilus influenzae strain Rd.” Biochem. Biophys. Res. Commun.2002‚ 295(1)‚ 1-8;}

 

^{16. Jianbo Zhang‚ Przemek Kowal‚ Jianwen Fang‚ Peter Andreana and Peng George Wang‚ “Efficient chemoenzymatic synthesis of globotriose and its derivatives with a recombinant a(1→4)-galactosyltransferase.” Carbohydr. Res. 2002‚ 337 (11)‚ 969-976;}

 

^{15. Ziye Liu‚ Jianbo Zhang‚ Xi Chen and Peng George Wang‚ “Combined biosynthetic pathway for de novo production of UDP-Galactose: Catalyzed with multiple enzymes immobilized on agarose beads.” ChemBioChem. 2002‚ 3‚ 348-355;}

 

^{14. Xi Chen‚ Ziye Liu‚ Jianbo Zhang‚ Wei Zhang‚ Przemek Kowal and Peng George Wang‚ “Reassemble biosynthetic pathways for large-scale carbohydrate synthesis: a-Gal epitope producing ‘superbug’.” ChemBioChem‚ 2002‚ 3‚ 47-53;}

 

^{13. Jianbo Zhang‚ Bingyuan Wu‚ Ziye Liu‚ Przemyslaw Kowal‚ Xi Chen‚ Jun Shao and Peng George Wang‚ “Large-scale synthesis of carbohydrates for pharmaceutical development.” Curr. Org. Chem. 2001‚5‚ 1169-1176;}

 

^{12. Xi Chen‚ Jianbo Zhang‚ Przemek Kowal‚ Ziye Liu‚ Peter R. Andreana‚ Yuquan Lu and Peng George Wang‚ “Transferring a biosynthetic cycle into a productive E. coli strain: large-scale synthesis of galactosides.” J. Am. Chem. Soc. 2001‚ 123‚ 8866-8867;}

 

^{11. Xi Chen‚ Jianwen Fang‚ Jianbo Zhang‚ Ziye Liu‚ Jun Shao‚ Przemyslaw Kowal‚ Peter Andreana and Peng George Wang‚ “Sugar nucleotide regeneration beads (superbeads): A versatile tool for the practical synthesis of oligosaccharides.” J. Am. Chem. Soc. 2001‚ 123‚ 2081-2082;}

 

^{10. Peng George Wang‚ Xi Chen‚ Ziye Liu and Jianbo Zhang‚ “Large scale production of oligosaccharides through superbug and superbeads technology”. Glycobiology 2001‚ 11‚ 34;}

 

^{9. Biao Yu‚ Jianchun Liao‚ Jianbo Zhang and Yongzheng Hui‚“The first synthetic route to furostan saponins.” Tetrahedron Lett. 2001‚ 42‚ 77-79;}

 

^{8. Jianbo Zhang‚ Biao Yu and Yongzheng Hui‚“Recent progresses in research of furostanol saponins.” Chinese J. Org. Chem.2000‚ 20‚ 663-688;}

 

^{7. Biao Yu‚ Jianbo Zhang‚ Shoufu Lu and Yongzheng Hui‚ “A novel and efficient deprotection of the allyl group at the anomeric oxygen of carbohydrates.” Synlett. 1998‚ 29-30;}

 

^{6. Biao Yu‚ Bing Li‚ Jianbo Zhang and Yongzheng Hui‚ “A novel cleavage of allyl protection”. Tetrahedron Lett. 1998‚ 39‚ 4871-4874;}

 

^{5. Jianbo Zhang and Gengyuan Tian‚ “High performance capillary electrophoresis of carbohydrates.”Chinese J. Org. Chem. 1998‚ 18‚ 88-96;}

 

^{4. Jianbo Zhang and Gengyuan Tian‚ “Progress in isolation and structural analysis of oligosaccharides.”Prog. Biochem. Biophys. 1998‚ 25‚ 114-119.}

 

^{Book Chapters}

 

^{3. Jianbo Zhang‚ “Degradations and Rearrangement Reactions” in Glycoscience‚ 2nd edition‚ Fraser-Reid‚ B.; Tatsuta‚ K.; Thiem‚ J. Eds; (edited by B. Fraser-Reid‚ K. Tatsuta‚ J. Thiem and G. Coté‚ S. Flitsch‚ Y. Ito‚ H.‚ Kondo‚ S.-I. Nishimura‚ B. Yu)‚ Springer Verlag GmbH‚ Heidelberg‚ 2008; p 375-426;}

 

^{2. Jianbo Zhang‚ Jun Shao‚ Przemek Kowal and Peng George Wang‚ “Enzymatic synthesis of oligosaccharides.” In: “Carbohydrate-Based Drug Discovery” C.-H. Wong‚ Ed‚ Wiley-VCH Press‚ Weinheim‚ 2003;p 137-167.}

 

^{1. Jianbo Zhang‚ Xi Chen‚ Jun Shao‚ Yuquan Lu and Peng George Wang‚ “Synthesis of galactose-containing oligosaccharides through “superbeads” and “superbug” approaches --- substrate recognition along different biosythetic pathways.” In: Methods in Enzymology‚ Vol 362‚ “Recognition of Carbohydrates in Biological Systems”‚ Y.-C. Li‚ Reiko T. Lee‚ Eds‚ Elsevier Science (USA)‚ 2003; p 106-125.}

 

Some Achievements Exposition:

Glycoconj. J., 2017, 34, 13-20.

 

Synlett, 2017, 28, 347-352.

 

J. Carbohydr. Chem., 2016, 35, 315-325