General

jiaowei,  Chengdu Institute of Biology, Chinese Academy of Sciences


Chengdu Institute of Biology, Chinese Academy of Sciences, No. 93, Keyuan South Road, Chengdu, Sichuan, China, 610041

E-mail: jiaowei@cib.ac.cn

Tel: +86 28 82890819

Zip code: 610041

Research Areas

medicinal chemistry and bioorganic chemistry

Education

École Polytechnique Fédérale de Lausanne,visitiing scholar, 2015

Chengdu Institute of Biology, Chinese Academy of Sciences, Chengdu, Sichuan, China, Ph.D. Pharmaceutical Chemistry, 2008;

University of Science and Technology of China, Hefei, Anhui, Joint postgraduate studies, 2003;

Inner Mongolia University, Inner Mongolia, China, B.A. Chemistry, 1998.


Publications

[1]     Yuan W., Xia J. H., Zhang X. K., Liang P., Zhang J. C., Jiao W., Shao, H. W., An efficient method for the stereoselective synthesis of N-substituted trihydroxypiperidine derivatives promoted by p-TsOH, 2016, Tetrahedron, 72, 3994–4000.

[2]     Jiao W.*, Wan Z. M., Chen S., Lu R. H., Chen X. Z., Fang D. M., Wang J. F., Pu S. C., Huang X., Gao H. X., Shao H. W., Lathyrol Diterpenes as Modulators of P-Glycoprotein Dependent Multidrug Resistance: Structure-Activity Relationship Studies on Euphorbia Factor L-3 Derivatives, J. Med. Chem., 58(9), 3720–3738, 2015.

[3]     Shen X. D., Xia J. H., Liang P., Ma X. F., Jiao W., Shao H. W., Zn(OTf)2 Promoted Rearrangement of 1,2-cyclopropanated Sugars with Amines: A Convenient Method for the Synthesis of 3-polyhydroxyalkyl-substituted Pyrrole Derivatives, Org. Biomol. Chem., 13(44), 10865-10873, 2015.

[4]     Jiao W., Wu Z. J., Chen X. Z., Lu R. H., Shao H. W., Rhopeptin A: First Cyclopeptide Isolated from Rhodobryum giganteum, Helv. Chim. Acta, 96, 114–118, 2013.

[5]     Jiao W.*, Chen X. Z., Wang H. B., Lu R. H., Shao H. W., A New Hepatotoxic Triterpenoid Ketone from Curculigo orchioides, Fitoterapia, 84, 1–5, 2013.

[6]     Jiao W., Fang D. M., Wu Z. J., Chen J. Z., Shao H. W., Zhang G. L., Analysis of Lathyrane Diterpenes Using Electrospray Ionization Quadrupole Time-of-flight Mass Spectrometry, Rapid Commun. Mass Spectrom., 27, 276–280, 2013.

[7]     Jiao W., Li Z. F., Dong W. W., Deng M. C., Lu R. H., Lathyrane Diterpenes from Euphorbia lathyris L. as Modulators of Multidrug Resistance and Their Crystal Structures, Bioorg. Med. Chem., 17, 4786–4792, 2009.

[8]     Jiao W., Yu K. B., Lu R. H., Configuration Confirmation of Euphorbia Factor L1 by Single-crystal X-ray Diffraction, Chin. J. Struct. Chem., 27(12), 1431–1434, 2008.

[9]     Jiao W., Mao Z. H., Dong W. W., Deng M. C., Lu R. H., Euphorbia Factor L8: a Diterpenoid from the Seeds of Euphorbia lathyris, Acta Crystallogr. E, 64, o331, 2008.

[10] Jiao W., Mao Z. H., Lu R. H., Euphorbia Factor L2: an Ester of 7−hydroxyLathyrol, Acta Crystallogr. E, 63, o4613, 2007.

[11] Wang Z. Z., Jiao W., He G. Y., Lu R. H., One-step Regioselective Green Synthesis of 2, 3-mannoepoxy-β-cyclodextrin under Aqueous Conditions, Mon. Chem., 140, 79–81, 2009.

[12] Dong W. W., Jiao W., Deng M. C., Yang C. B., Yue J. M., Lu R. H., A New Steroid Glycoside Derivative from Acorus calamus L., J. Chin. Chem. Soc., 55, 1277–1279, 2008.

[13] Wang X. L., Jiao W., Liao X., Peng S. L., Ding L. S., Monoterpene Glycosides from the Roots of Paeonia lactiflora, Chin. Chem. Lett., 17(7), 916–918, 2006.

[14] Deng M. C., Dong W. W., Jiao W., Lu R. H., New Eremophilane Sesquiterpenes from the Roots of Ligularia fischeri, Helv. Chim. Acta, 92, 3, 495–501, 2009.

[15] Wang X. L., Gesang S. L., Jiao W., Liao X., Ding L. S., Two New Sesquiterpenoid Glucosides from the Aerial Parts of Saussurea involucrate, J. Integr. Plant Biol., 49(5), 609–614, 2007. ​

[16] Chen X. Z., Lu S. M., Li G. Y., Jiao W., Huang T. F., Yang T., Fang D. M., Biphenyls from Aerial Parts of Ribes takare, Chin. Chem. Lett., 25(1), 127–130, 2014.

[17] Wang C., Ma X. F., Zhang J. C., Tang Q., Jiao W., Shao H. W., Methanesulfonic-Acid-Catalysed Ring Opening and Glycosylation of 1,2-(Acetylcyclopropane)-Annulated D-Lyxofuranose, Eur. J. Org. Chem., 21, 4592–4599, 2014.

[18]     Shen X. D., Xia J. H., Liang P., Ma X. F., Jiao W., Shao H. W., Zn(OTf)2 Promoted Rearrangement of 1,2-cyclopropanated Sugars with Amines: A Convenient Method for the Synthesis of 3-polyhydroxyalkyl-substituted Pyrrole Derivatives, Org. Biomol. Chem., 13(44), 10865-10873, 2015.

[19] Lu R. H., Yang C. , Cao Y. J., Tong H. L., Jiao W., Wada T., Wang Z. Z., Mori T., Inoue Y., Enantiodifferentiating Photoisomerization of Cyclooctene Included and Sensitized by Aroyl-beta-Cyclodextrins: A Critical Enantioselectivity Control by Substituents, J. Org. Chem., 73, 7695–7701, 2008.


Students

现指导学生

向玲  硕士研究生  085235-制药工程  

杨春梅  硕士研究生  085238-生物工程  

唐森铃  硕士研究生  086000-生物与医药