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Zhizhong Wang, Xueyan Fu, Guidong Dai, Hongfeng Quan
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Efficient and improved syntheses of two key intermediates for functionalization of ¦Â-cyclodextrin at the secondary hydroxyl face
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Monatsh. Chem., 2011, 142: 317-319
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Efficient and improved syntheses of two key intermediates for functionalization of beta-cyclodextrin at the secondary hydroxyl face
×÷Õß:Wang, ZZ (Wang, Zhi-zhong)[ 1,2 ] ; Fu, XY (Fu, Xue-yan)[ 2 ] ; Dai, GD (Dai, Gui-dong)[ 2 ] ; Quan, HF (Quan, Hong-feng)[ 2 ]


MONATSHEFTE FUR CHEMIE


¾í: 142
ÆÚ: 3
Ò³: 317-319
DOI: 10.1007/s00706-011-0451-4

³ö°æÄê: MAR 2011

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MONATSHEFTE FUR CHEMIE  

³ö°æÉÌ SPRINGER WIEN, SACHSENPLATZ 4-6, PO BOX 89, A-1201 WIEN, AUSTRIA

ISSN: 0026-9247

Ñо¿ÁìÓò Chemistry



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A new and improved method for the regioselective synthesis of mono-2-tosyl-beta-cyclodextrin was achieved under aqueous conditions that do not require large amounts of polar organic solvents such as N,N-dimethylformamide (DMF), specific basic catalysts such as Cs(2)CO(3), or flammable bases such as NaH. Moreover, mono-2,3-mannoepoxy-beta-cyclodextrin was also synthesized in the same reaction system by prolonging the reaction time.

¹Ø¼ü´Ê
×÷Õ߹ؼü´Ê:Cyclodextrin; Mono-2-tosyl-beta-cyclodextrin; Mono-2,3-mannoepoxy-beta-cyclodextrin; Regioselective synthesis

KeyWords Plus:BIOMIMETIC CHEMISTRY; SULFONYLATION; DERIVATIVES; ENZYMES

×÷ÕßÐÅÏ¢
ͨѶ×÷ÕßµØÖ·: Wang, ZZ (ͨѶ×÷Õß) Ningxia Med Univ, Sch Pharm, Yinchuan 750004, Peoples R China.
  ÔöÇ¿×éÖ¯ÐÅÏ¢µÄÃû³Æ
    Ningxia Medical University  


µØÖ·:  [ 1 ] Ningxia Med Univ, Sch Pharm, Yinchuan 750004, Peoples R China
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    Ningxia Medical University  
       [ 2 ] Ningxia Engn Res Ctr Hui Med Modernizat, Yinchuan 750004, Peoples R China


µç×ÓÓʼþµØÖ·:wangzzsc@yahoo.com

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Natural Science Foundation of Ningxia Medical University  XT201001  
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Financial support from the Natural Science Foundation of Ningxia Medical University (No. XT201001) is gratefully acknowledged.

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SPRINGER WIEN, SACHSENPLATZ 4-6, PO BOX 89, A-1201 WIEN, AUSTRIA

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Ñо¿·½Ïò:Chemistry

Web of Science Àà±ð:Chemistry, Multidisciplinary

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ÓïÖÖ:English

Èë²ØºÅ: WOS:000288511500013

ISSN: 0026-9247

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Web of Science ºËÐĺϼ¯ÖÐµÄ "ÒýÓõIJο¼ÎÄÏ×": 23

Web of Science ºËÐĺϼ¯ÖÐµÄ "±»ÒýƵ´Î": 2

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Efficient and improved syntheses of two key intermediates for functionalization of beta-cyclodextrin at the secondary hydroxyl face
×÷Õß:Wang, ZZ (Wang, Zhi-zhong)[ 1,2 ] ; Fu, XY (Fu, Xue-yan)[ 2 ] ; Dai, GD (Dai, Gui-dong)[ 2 ] ; Quan, HF (Quan, Hong-feng)[ 2 ]
MONATSHEFTE FUR CHEMIE
¾í: 142  ÆÚ: 3  Ò³: 317-319
DOI: 10.1007/s00706-011-0451-4
³ö°æÄê: MAR 2011
²é¿´ÆÚ¿¯ÐÅÏ¢
ÕªÒª
A new and improved method for the regioselective synthesis of mono-2-tosyl-beta-cyclodextrin was achieved under aqueous conditions that do not require large amounts of polar organic solvents such as N,N-dimethylformamide (DMF), specific basic catalysts such as Cs(2)CO(3), or flammable bases such as NaH. Moreover, mono-2,3-mannoepoxy-beta-cyclodextrin was also synthesized in the same reaction system by prolonging the reaction time.
¹Ø¼ü´Ê
×÷Õ߹ؼü´Ê:Cyclodextrin; Mono-2-tosyl-beta-cyclodextrin; Mono-2,3-mannoepoxy-beta-cyclodextrin; Regioselective synthesis
KeyWords Plus:BIOMIMETIC CHEMISTRY; SULFONYLATION; DERIVATIVES; ENZYMES
×÷ÕßÐÅÏ¢
ͨѶ×÷ÕßµØÖ·: Wang, ZZ (ͨѶ×÷Õß)
Òþ²ØÔöÇ¿×éÖ¯ÐÅÏ¢µÄÃû³Æ        Ningxia Med Univ, Sch Pharm, Yinchuan 750004, Peoples R China.
  ÔöÇ¿×éÖ¯ÐÅÏ¢µÄÃû³Æ
     Ningxia Medical University
µØÖ·:
Òþ²ØÔöÇ¿×éÖ¯ÐÅÏ¢µÄÃû³Æ        [ 1 ] Ningxia Med Univ, Sch Pharm, Yinchuan 750004, Peoples R China
  ÔöÇ¿×éÖ¯ÐÅÏ¢µÄÃû³Æ
     Ningxia Medical University
              [ 2 ] Ningxia Engn Res Ctr Hui Med Modernizat, Yinchuan 750004, Peoples R China
µç×ÓÓʼþµØÖ·:wangzzsc@yahoo.com
»ù½ð×ÊÖúÖÂл
»ù½ð×ÊÖú»ú¹¹        ÊÚȨºÅ
Natural Science Foundation of Ningxia Medical University        
XT201001
²é¿´»ù½ð×ÊÖúÐÅÏ¢   
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SPRINGER WIEN, SACHSENPLATZ 4-6, PO BOX 89, A-1201 WIEN, AUSTRIA
Àà±ð / ·ÖÀà
Ñо¿·½Ïò:Chemistry
Web of Science Àà±ð:Chemistry, Multidisciplinary
ÎÄÏ×ÐÅÏ¢
ÎÄÏ×ÀàÐÍ:Article
ÓïÖÖ:English
Èë²ØºÅ: WOS:000288511500013
ISSN: 0026-9247
ÆÚ¿¯ÐÅÏ¢
Impact Factor (Ó°ÏìÒò×Ó): Journal Citation Reports®
ÆäËûÐÅÏ¢
IDS ºÅ: 736RJ
Web of Science ºËÐĺϼ¯ÖÐµÄ "ÒýÓõIJο¼ÎÄÏ×": 23
Web of Science ºËÐĺϼ¯ÖÐµÄ "±»ÒýƵ´Î": 2
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