½Î÷ʦ´ó¹ú¼Òµ¥ÌÇÖÐÐĺúÏé¹úµ¼Ê¦ÕÐÊÕ2019ÄêÓлú/Ò©Îﻯѧ˶ʿµ÷¼ÁÉú2Ãû£¡£¡£¡
ÎÒÃÇ¿ÎÌâ×éÕÐÊÕ2019ÄêÓлú/Ò©Îﻯѧ˶ʿµ÷¼ÁÉú2Ãû£¬ÒªÇó³É¼¨´ïµ½¹ú¼ÒÏߣ¨aÀࣩ, ÄÐÉú£¨ÏÖÔÚÅ®ÉúÃû¶îÒÑÂú£©£¬Ó¢Óï¹ýËļ¶£¬³É¼¨ÔÚ330ÒÔÉÏ£¬¶¯ÊÖÄÜÁ¦Ç¿, ÔÚ±¾¿ÆÆÚ¼ä´Óʹý¿ÆÑÐʵϰ»òÑо¿ÕßÓÅÏÈ¿¼ÂÇ.
ÈȳÀ»¶ÓÕâ´Î¿¼Ñз¢»Óʧ³££¬µ«ÓÐÖ¾ÓÚ¿ÆÑÐÊÂÒµµÄÄêÇáѧ×Ó¼ÓÈëµ½ÎÒÃÇ¿ÎÌâ×飡ÎÒÃÇ¿ÎÌâ×龷ѳä×ã¡¢É豸һÁ÷£¬ÇÒÓë¹úÄÚÍâ¸ßˮƽʵÑéÊÒ¾ßÓÐÓÅÁ¼µÄºÏ×÷»ù´¡£¬ÎÒÃǽ«Îª³É¼¨ÓÅÐ㣬½øÈ¡ÐÄÇ¿µÄѧÉúÌṩµ½¹úÄÚÍâÒ»Á÷ʵÑéÊÒÁªºÏÅàÑøºÍ¼ÌÐøÉîÔìµÄ»ú»á¡£ÀÏʦÿÔ·¢×ã¹»Éú»î²¹ÖúÒÔÈ·±£Ñ§ÉúÄܹ»×¨ÐÄ´ÓÊ¿ÆÑÐ.
ÁªÏµÈË£º
×ÞÁ¼¾²Ê¦ÐÖ µç»°£º15170498613 qq: 1264428424
Ê·ÎÄÔóʦÐÖ µç»°£º15970445200 qq: 2014684503 ÓÊÏ䣺18772395200@163.com
£¨¸ü¶àʦÐÖʦ½ãÁªÏµÐÅÏ¢Çë¼û¿ÎÌâ×éÖ÷Ò³£©
¼òÀúÇëÖ±½Ó·¢ËÍÁ½·Ý¡£
¼òÀú°üÀ¨£º¸öÈ˼ò½é£» ѧҵ±³¾°£¬ÊÇ·ñÓ¦½ì£»¿ÆÑоÀú£¨¼òÃ÷¶óÒª¼´¿É£©£»¿¼Ñгɼ¨µ¥£¨¸÷¿Æ³É¼¨£¬±¨¿¼ÔºÐ£¼°×¨Òµ£©£»Ó¢Óï³É¼¨Ö¤Ã÷£¨ËÄÁù¼¶³É¼¨£©£»±¾¿ÆÆÚ¼äËùÐ޴󲿷ÖÖ÷¸Éרҵ¿Î£¨Ö÷ÒªÊÇÁ˽âÒ»ÏÂÐÞ¹ýʲô¿Î³Ì£©£»ÁªÏµ·½Ê½£¨µç»°¼°qq£©
¿ÎÌâ×éÖ÷Ò³Á´½Ó£ºhttp://www.escience.cn/people/xiangguohu/index.html
µ¼Ê¦¼ò½é£¨ÏêϸÐÅÏ¢Çë¼û¿ÎÌâ×éÖ÷Ò³£©£º
ºúÏé¹ú£¬½Î÷ʦ·¶´óѧ¹ú¼Òµ¥ÌÇÖÐÐÄÌØƸ½ÌÊÚ£¬½Î÷Ê¡½Ü³öÇàÄ꣨2017£©¡£2005Äê6ÔÂÏæ̶´óѧ»ñ¹¤Ñ§Ñ§Ê¿Ñ§Î»£¬Í¬Äê9Ô±£ËͽøÈëÖйú¿ÆѧԺ»¯Ñ§Ñо¿Ëù£¬2010Äê»ñÀíѧ²©Ê¿Ñ§Î»¡£²©Ê¿ÆÚ¼äÖ÷Òª´ÓÊÂË«»·¶àôÇ»ùÉúÎï¼îµÄÈ«ºÏ³É¼°»îÐÔÑо¿¹¤×÷¡£2010Äê8ÔÂ-2012Äê8ÔÂÖйú¿ÆѧԺ»¯Ñ§Ñо¿ËùÖúÀíÑо¿Ô±£¬Ö÷Òª´ÓÊ»îÐÔÑÇ°·ÌÇ·Ö×ÓÉè¼ÆÓëºÏ³É¼°ÑÇ°·ÌÇÒ©ÎïµÄ¹¤ÒÕÑо¿¡£2012Äê8ÔÂ-2015Äê3ÔÂÔÚÐÂÄÏÍþ¶ûÊ¿´óѧ½øÐв©Ê¿ºóÑо¿£¬2015Äê3Ô¼ÓÃ˽Î÷ʦ·¶´óѧ¹ú¼Òµ¥ÌÇÖÐÐĽøÐнÌѧ¿ÆÑй¤×÷¡£Æù½ñÔÚ¹ú¼Ê¸ßˮƽÔÓÖ¾angew.chem. int. ed, org. lett, j. org. chem. green chem.µÈ¹ú¼ÊÆÚ¿¯·¢±íÂÛÎÄ24ƪ£¬ÉêÇëÊÚȨ·¢Ã÷רÀû10ÓàÏËù¿ª·¢µÄÖÎÁÆÌÇÄò²¡Ò©ÎïÃ׸ñÁд¼µÄй¤ÒÕÒѱ»Õã½°ÂÏèÒ©Òµ²ÉÓò¢ÖÐÊÔÉú²ú¡£Ö÷ÒªÑо¿ÐËȤΪÌÇ»¯Ñ§¡¢Óлú·ú»¯Ñ§.
´ú±íÐÔÂÛÎÄ£¨ÏêϸÐÅÏ¢Çë¼û¿ÎÌâ×éÖ÷Ò³£©£º
1. zhang, x.-w.; hu, w.-l.; chen, s.; hu, x.-g.*, cu-catalyzed synthesis of fluoroalkylated isoxazoles from commercially available amines and alkynes. org. lett. 2018, 20, 860-863.
2. gao, f.-t.; fang, z.; su, r.-r.; rui, p.-x.; hu, x.-g.*, hydroximoyl fluorides as the precursors of nitrile oxides: synthesis, stability and [3 + 2]-cycloaddition with alkynes. org. biomol. chem. 2018, 16, 9211-9217.
3. wang, h.; tu, y.-h.; liu, d.-y.; hu, x.-g., cu-catalyzed/mediated synthesis of n-fluoroalkylanilines from arylboronic acids: fluorine effect on the reactivity of fluoroalkylamines. org. biomol. chem. 2018, 16, 6634-6637.
4. gao, y.; peng, s.; liu, d.; rui, p.; hu, x.-g., copper-catalyzed four component reaction for the synthesis of n-difluoroethyl imides. eur. j. org. chem. 10.1002/ejoc.201801334.
5. liu, t.; yan, n.; zhao, h.; wang, z.-x.; hu, x.-g. *, synthesis and antibacterial activity of 6(r)- and 6(s)-fluoropenibruguieramine as: fluorine as a probe for testing the powerfulness of memory of chirality (moc). j. fluorine chem. 2018, 207, 18-23.
6. peng, s. q.; zhang, x. w.; zhang, l.; hu, x. g. *, esterification of carboxylic acids with difluoromethyl diazomethane and interrupted esterification with trifluoromethyl diazomethane: a fluorine effect. org. lett. 2017, 19, 5689-5692.
7. yan, n.; lei, z. w.; su, j. k.; liao, w. l.; hu, x. g. *, ring opening of sugar-derived epoxides by tbaf/khf2: an attractive alternative for the introduction of fluorine into the carbohydrate scaffold. chin. chem. lett. 2017, 28, 467-470.
8. hu, w.-l.; hu, x.-g. *; hunter, l., recent developments in the deoxyfluorination of alcohols and phenols: new reagents, mechanistic insights, and applications. synthesis 2017, 49, 4917-4930.
9. fang, z.; hu, w. l.; liu, d. y.; yu, c. y.; hu, x. g. *, synthesis of tetrazines from gem-difluoroalkenes under aerobic conditions at room temperature. green chem. 2017, 19, 1299-1302.
10. zhao, h.; hu, x.-g. *; xu, m.-j.; cai, q.-x.; liu, y.-j.; su, d.-m.; chen, s.-j.; wang, k.; gong, z.-n., six-step synthesis of leonurine and toxicity study on zebrafish. chin. chem. lett. 2017, 28, 1172-1175.
11. yan, n.; fang, z.; liu, q.-q.; guo, x.-h.; hu, x.-g. *, conformation-induced regioselective and divergent opening of epoxides by fluoride: facile access to hydroxylated fluoro-piperidines. org. biomol. chem. 2016, 14, 3469-3475.
12. hu, x. g. ; lawer, a.; peterson, m. b.; iranmanesh, h.; ball, g. e.; hunter, l., diastereoselective synthesis and conformational analysis of (2r)- and (2s)-fluorostatines: an approach based on organocatalytic fluorination of a chiral aldehyde. org. lett. 2016, 18, 662-665.
13. hu, x. g.; thomas, d. s.; griffith, r.; hunter, l., stereoselective fluorination alters the geometry of a cyclic peptide: exploration of backbone-fluorinated analogues of unguisin a. angew. chem. int. ed. 2014, 53, 6176-6179.
[ Last edited by Walter-swz on 2019-3-20 at 08:47 ] |