±±¾©Ê¯ÓÍ»¯¹¤Ñ§Ôº2026ÄêÑо¿ÉúÕÐÉú½ÓÊÕµ÷¼Á¹«¸æ
²é¿´: 234  |  »Ø¸´: 1

zengjundeyo

Ö÷¹ÜÇø³¤

ÓÅÐ㣡£¡ÓÐľÓУ¡£¡£¡ÓÅÐ㣡£¡ÓÐľÓУ¡£¡£¡ÓÅÐ㣡£¡ÓÐľÓУ¡£¡£¡ÓÅÐ㣡£¡ÓÐľÓУ¡£¡£¡

[ÇóÖú] Çó΢Æ×²éѯһ¸ö»¯ºÏÎï

CDCl3ÖÐ:7.8,21.3,30.1,31.0,31.1,38.0,43.0,44.2,51.2,51.6,52.0,52.4,53.4,55.7,66.7,76.6,79.8,83.6,93.5,119.0,121.3,124.2,124.7,130.4,153.2,158.0,171.7,172.0,178.8
»Ø¸´´ËÂ¥

» ²ÂÄãϲ»¶

» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:

ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

ÅËÏÜΰ

°æÖ÷

ÓÅÐ㣡£¡ÓÐľÓУ¡£¡£¡ÓÅÐ㣡£¡ÓÐľÓУ¡£¡£¡ÓÅÐ㣡£¡ÓÐľÓУ¡£¡£¡ÓÅÐ㣡£¡ÓÐľÓУ¡£¡£¡

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
zengjundeyo: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-03-05 09:39:11
²éѯ½á¹û£º¹²²éµ½33¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)  
--------------------------------------------------------------------------------

1 .     bannucine
    ÏàËÆ¶È:93.1%
Journal of the Chemical Society, Perkin Transactions 1          1986                   923-926
Bannucine ¨C a new dihydroindole alkaloid from Catharanthus roseus(L) G.Don
Atta-ur-Rahman, Irshad Ali and M. Iqbal Chaudhary
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

2 .     compound 3a
C31H36N2O6     ÏàËÆ¶È:82.7%
Heterocycles          2005          65          165-171
Preparation of New Vindoline Derivatives by Palladium-catalyzed Cross-Coupling Reaction
Melinda Fekete, Pal Kolonits, and Lajos Novak*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

3 .     compound 3e
C31H34N2O6F2     ÏàËÆ¶È:82.7%
Heterocycles          2005          65          165-171
Preparation of New Vindoline Derivatives by Palladium-catalyzed Cross-Coupling Reaction
Melinda Fekete, Pal Kolonits, and Lajos Novak*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

4 .     Vindolicine
    ÏàËÆ¶È:82.7%
Organic Magnetic Resonance          1976          8          413-418
13C n.m.r. spectroscopy: Comparison of the spectra of some dimeric Catharanthus alkaloids and their derivatives
Douglas E. Dorman and Jonathan W. Paschal
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

5 .     compound 3d
C31H35N3O8     ÏàËÆ¶È:80.6%
Heterocycles          2005          65          165-171
Preparation of New Vindoline Derivatives by Palladium-catalyzed Cross-Coupling Reaction
Melinda Fekete, Pal Kolonits, and Lajos Novak*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

6 .     compound 3f
C33H34N2O6F6     ÏàËÆ¶È:80%
Heterocycles          2005          65          165-171
Preparation of New Vindoline Derivatives by Palladium-catalyzed Cross-Coupling Reaction
Melinda Fekete, Pal Kolonits, and Lajos Novak*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

7 .     compound 3c
C37H40N2O7     ÏàËÆ¶È:75.7%
Heterocycles          2005          65          165-171
Preparation of New Vindoline Derivatives by Palladium-catalyzed Cross-Coupling Reaction
Melinda Fekete, Pal Kolonits, and Lajos Novak*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

8 .     compound 3b
C32H38N2O6     ÏàËÆ¶È:73.3%
Heterocycles          2005          65          165-171
Preparation of New Vindoline Derivatives by Palladium-catalyzed Cross-Coupling Reaction
Melinda Fekete, Pal Kolonits, and Lajos Novak*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

9 .     vindorosine
    ÏàËÆ¶È:72.4%
Acta Pharmaceutica Sinica          2010          45          471-474
Monomeric indole alkaloids from the aerial parts of Catharanthus roseus
ZHONG Xiang-zhang, WANG Guo-cai, WANG Ying, ZHANG Xiao-qi, YE Wen-cai*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

10 .     vindoline
    ÏàËÆ¶È:72.4%
Acta Pharmaceutica Sinica          2010          45          471-474
Monomeric indole alkaloids from the aerial parts of Catharanthus roseus
ZHONG Xiang-zhang, WANG Guo-cai, WANG Ying, ZHANG Xiao-qi, YE Wen-cai*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

11 .     vindoline
    ÏàËÆ¶È:68.9%
Journal of Natural Products          1983          Vol 46          517-527
Catharanthus Alkaloids, XXXVIII. Confirming Structural Evidence and Antineoplastic Activity of the Bisindole Alkaloids Leurosine-N'b-Oxide (Pleurosine), Roseadine, and Vindolicine from Catharanthus roseus
Aly El-Sayed, George A. Handy, Geoffrey A. Cordell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

12 .     15-iodovindoline
C25H31N2O6I     ÏàËÆ¶È:68.9%
Heterocycles          2005          65          165-171
Preparation of New Vindoline Derivatives by Palladium-catalyzed Cross-Coupling Reaction
Melinda Fekete, Pal Kolonits, and Lajos Novak*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

13 .     Vindoline
    ÏàËÆ¶È:68.9%
Organic Magnetic Resonance          1976          8          413-418
13C n.m.r. spectroscopy: Comparison of the spectra of some dimeric Catharanthus alkaloids and their derivatives
Douglas E. Dorman and Jonathan W. Paschal
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

14 .     3-Demethoxycarbonyl-3-(3',3'-dimethylbutyramino)methylvindoline
    ÏàËÆ¶È:65.5%
Journal of Natural Products          2009          72          1170-1177
Synthesis and Structure-Activity Relationship Studies of Cytotoxic Anhydrovinblastine Amide Derivatives
Yong Shao, Han-Kun Zhang,Hong Ding, Hai-Tian Quan, Li-Guang Lou, and Li-Hong Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

15 .     compound 3
    ÏàËÆ¶È:65.5%
Chemistry of Natural Compounds          1986          22          1-13
APPLICATIONS OF 1H AND 13C NMR SPECTROSCOPY IN STRUCTURAL INVESTIGATIONS OF Vinca INDOLE ALKALOIDS
M. R. Yagudaev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

16 .     10-chlorovindoline
C25H31ClN2O6     ÏàËÆ¶È:65.5%
Heterocycles          2007          71          1553-1563
Aromatic Electrophilic Substitutions on Vindoline
¨¢lmos Gorka-Keresk¨¦nyi, Lajos Szab¨®, L¨¢szl¨® Hazai, Mikl¨®s Lengyel, Csaba Sz¨¢ntay, Jr., Zsuzsanna S¨¢nta, György Kalaus, and Csaba Sz¨¢ntay
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

17 .     10-bromovindoline
C25H31N2O6Br     ÏàËÆ¶È:62.0%
Heterocycles          2007          71          1553-1563
Aromatic Electrophilic Substitutions on Vindoline
¨¢lmos Gorka-Keresk¨¦nyi, Lajos Szab¨®, L¨¢szl¨® Hazai, Mikl¨®s Lengyel, Csaba Sz¨¢ntay, Jr., Zsuzsanna S¨¢nta, György Kalaus, and Csaba Sz¨¢ntay
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

18 .     3-Demethoxycarbonyl-3-(pyridine-4'-carbonylamino)methylvindoline
    ÏàËÆ¶È:58.6%
Journal of Natural Products          2009          72          1170-1177
Synthesis and Structure-Activity Relationship Studies of Cytotoxic Anhydrovinblastine Amide Derivatives
Yong Shao, Han-Kun Zhang,Hong Ding, Hai-Tian Quan, Li-Guang Lou, and Li-Hong Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

19 .     3-Demethoxycarbonyl-3-(4'-nitrobenzoylamino)methylvindoline
    ÏàËÆ¶È:58.6%
Journal of Natural Products          2009          72          1170-1177
Synthesis and Structure-Activity Relationship Studies of Cytotoxic Anhydrovinblastine Amide Derivatives
Yong Shao, Han-Kun Zhang,Hong Ding, Hai-Tian Quan, Li-Guang Lou, and Li-Hong Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

20 .     3-Demethoxycarbonyl-3-(4'-methoxybenzoylamino)methylvindoline
    ÏàËÆ¶È:56.6%
Journal of Natural Products          2009          72          1170-1177
Synthesis and Structure-Activity Relationship Studies of Cytotoxic Anhydrovinblastine Amide Derivatives
Yong Shao, Han-Kun Zhang,Hong Ding, Hai-Tian Quan, Li-Guang Lou, and Li-Hong Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

21 .     3-Demethoxycarbonyl-3-(3'-methylbutyramino)methylvindoline
    ÏàËÆ¶È:55.1%
Journal of Natural Products          2009          72          1170-1177
Synthesis and Structure-Activity Relationship Studies of Cytotoxic Anhydrovinblastine Amide Derivatives
Yong Shao, Han-Kun Zhang,Hong Ding, Hai-Tian Quan, Li-Guang Lou, and Li-Hong Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

22 .     3-Demethoxycarbonyl-3-(4'-chlorobenzoylamino)methylvindoline
    ÏàËÆ¶È:55.1%
Journal of Natural Products          2009          72          1170-1177
Synthesis and Structure-Activity Relationship Studies of Cytotoxic Anhydrovinblastine Amide Derivatives
Yong Shao, Han-Kun Zhang,Hong Ding, Hai-Tian Quan, Li-Guang Lou, and Li-Hong Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

23 .     3-Demethoxycarbonyl-3-(4'-fluorobenzoylamino)methylvindoline
    ÏàËÆ¶È:53.3%
Journal of Natural Products          2009          72          1170-1177
Synthesis and Structure-Activity Relationship Studies of Cytotoxic Anhydrovinblastine Amide Derivatives
Yong Shao, Han-Kun Zhang,Hong Ding, Hai-Tian Quan, Li-Guang Lou, and Li-Hong Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

24 .     3-Demethoxycarbonyl-3-(phenylacetylamino)methylvindoline
    ÏàËÆ¶È:53.3%
Journal of Natural Products          2009          72          1170-1177
Synthesis and Structure-Activity Relationship Studies of Cytotoxic Anhydrovinblastine Amide Derivatives
Yong Shao, Han-Kun Zhang,Hong Ding, Hai-Tian Quan, Li-Guang Lou, and Li-Hong Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

25 .     zumsenin
C30H36O8     ÏàËÆ¶È:53.3%
Journal of Natural Products          2005          68          244-247
Insect Antifeedants from Croton jatrophoides:Structures of Zumketol, Zumsenin, and Zumsenol
Ken-ichi Nihei, Yukihiro Asaka, Yoshihiro Mine, and Isao Kubo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

26 .     3-Demethoxycarbonyl-3-(2'-methoxybenzoylamino)methylvindoline
    ÏàËÆ¶È:53.1%
Journal of Natural Products          2009          72          1170-1177
Synthesis and Structure-Activity Relationship Studies of Cytotoxic Anhydrovinblastine Amide Derivatives
Yong Shao, Han-Kun Zhang,Hong Ding, Hai-Tian Quan, Li-Guang Lou, and Li-Hong Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
רҵ
2Â¥2013-03-04 22:20:04
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
Ïà¹Ø°æ¿éÌø×ª ÎÒÒª¶©ÔÄÂ¥Ö÷ zengjundeyo µÄÖ÷Ìâ¸üÐÂ
×î¾ßÈËÆøÈÈÌûÍÆ¼ö [²é¿´È«²¿] ×÷Õß »Ø/¿´ ×îºó·¢±í
[¿¼ÑÐ] 085602»¯Ñ§¹¤³Ì268·Ö¶×µ÷¼Á +5 ÔÂÕÕ»¨ÁÖ¡£ 2026-04-01 5/250 2026-04-01 11:39 by ms629
[¿¼ÑÐ] 282Çóµ÷¼Á +12 ycy1201 2026-04-01 14/700 2026-04-01 11:20 by wangjy2002
[¿¼ÑÐ] »¯Ñ§0703 µ÷¼Á 306·Ö Ò»Ö¾Ô¸211 +12 26ÒªÉϰ¶ 2026-03-28 12/600 2026-04-01 11:10 by chemdavid
[¿¼ÑÐ] 085600£¬²ÄÁÏÓ뻯¹¤321·Ö£¬Çóµ÷¼Á +10 ´ó²öС×Ó 2026-03-27 10/500 2026-04-01 09:27 by oooqiao
[¿¼ÑÐ] 311£¨085601£©Çóµ÷¼Á +12 liziyeyeye 2026-03-28 13/650 2026-04-01 00:34 by fmesaito
[¿¼ÑÐ] ½­ËÕËÕ±±¸ßУ³ÏÑûµ÷¼Áͬѧ +3 zzll406 2026-03-31 3/150 2026-03-31 16:54 by ¼°Ê±ÐÐÀÖfan
[¿¼ÑÐ] Ò»Ö¾Ô¸Î人Àí¹¤£¬×Ü·Ö321£¬Ó¢Ò»Êý¶þ£¬ÇóÀÏʦÊÕÁô¡£ +12 nnnnnnn5 2026-03-25 12/600 2026-03-31 16:21 by ¼Çʱ¾2026
[¿¼ÑÐ] 277¹òÇóµ÷¼Á +8 1915668 2026-03-27 13/650 2026-03-31 14:58 by ÍõÁÁ_´óÁ¬Ò½¿Æ´ó
[¿¼ÑÐ] 282Çóµ÷¼Á +3 ºôÎü¶¼ÊǼõ·Ê 2026-03-31 3/150 2026-03-31 10:00 by wangjy2002
[¿¼ÑÐ] 0703»¯Ñ§321·ÖÇóµ÷¼Á +10 Èýdd. 2026-03-30 11/550 2026-03-30 19:24 by markhwc
[¿¼ÑÐ] 295²ÄÁϹ¤³Ìר˶Çóµ÷¼Á +10 1428151015 2026-03-27 10/500 2026-03-30 19:00 by Ô´_2020
[¿¼ÑÐ] 292Çóµ÷¼Á +13 ÊÇåû×ÓÒ²ÊÇÑÐ×Ó 2026-03-30 13/650 2026-03-30 18:01 by СÐì0109
[¿¼ÑÐ] 324Çóµ÷¼Á +9 hanamiko 2026-03-26 11/550 2026-03-30 14:27 by JourneyLucky
[¿¼ÑÐ] 311Çóµ÷¼Á +10 lin0039 2026-03-26 10/500 2026-03-30 10:26 by herarysara
[¿¼ÑÐ] 291Çóµ÷¼Á +5 Y-cap 2026-03-29 6/300 2026-03-29 13:18 by mumin1990
[¿¼ÑÐ] 0856£¬²ÄÁÏÓ뻯¹¤321·ÖÇóµ÷¼Á +12 ´ó²öС×Ó 2026-03-27 13/650 2026-03-28 10:56 by self2008
[¿¼ÑÐ] 0856µ÷¼Á +5 ÇóÇóÈÃÎÒÓÐÊé¶Á° 2026-03-26 6/300 2026-03-27 15:12 by caszguilin
[¿¼ÑÐ] ¸´ÊÔµ÷¼Á£¬Ò»Ö¾Ô¸ÄÏÅ©083200ʳƷ¿ÆÑ§Ó빤³Ì +5 XQTJZ 2026-03-26 5/250 2026-03-27 14:49 by ¿ñìÅÂóµ±µ±
[¿¼ÑÐ] µ÷¼Á +3 Àî¼Îͼ¡¤S¡¤Â· 2026-03-27 3/150 2026-03-27 11:19 by wangjy2002
[¿¼ÑÐ] 286Çóµ÷¼Á +4 lim0922 2026-03-26 4/200 2026-03-27 10:28 by guoweigw
ÐÅÏ¢Ìáʾ
ÇëÌî´¦ÀíÒâ¼û