Znn3bq.jpeg
±±¾©Ê¯ÓÍ»¯¹¤Ñ§Ôº2026ÄêÑо¿ÉúÕÐÉú½ÓÊÕµ÷¼Á¹«¸æ
²é¿´: 432  |  »Ø¸´: 1

qiaochunlin

гæ (³õÈëÎÄ̳)

[ÇóÖú] ΢Æ×ÇóÖú£¬Ð»Ð» ÒÑÓÐ1È˲ÎÓë

C13NMR(CDCL3):
15.4,15.8,21.3,28.8,32.7,37.4,52.2,126.6,126.8,136.2,140.5,145.8,146.4,148.6,149.3,149.8,152.4,167.0,167.3
ÒÑÃ÷È·ËùÇ󻯺ÏÎïÊÇÎÞɫ͸Ã÷ÒºÌå×´ÉúÎï¼î£¬ÉÏ´«¸½¼þΪËùÇ󻯺ÏÎïµÄ̼Æ×ºÍÇâÆ×µÄÆ×ͼ
»Ø¸´´ËÂ¥

» ±¾Ìû¸½¼þ×ÊÔ´Áбí

  • »¶Ó­¼à¶½ºÍ·´À¡£ºÐ¡Ä¾³æ½öÌṩ½»Á÷ƽ̨£¬²»¶Ô¸ÃÄÚÈݸºÔð¡£
    ±¾ÄÚÈÝÓÉÓû§×ÔÖ÷·¢²¼£¬Èç¹ûÆäÄÚÈÝÉæ¼°µ½ÖªÊ¶²úȨÎÊÌ⣬ÆäÔðÈÎÔÚÓÚÓû§±¾ÈË£¬Èç¶Ô°æÈ¨ÓÐÒìÒ飬ÇëÁªÏµÓÊÏ䣺xiaomuchong@tal.com
  • ¸½¼þ 1 : GHZ-8_H1_CDCl3_2015-4-30.fid.rar
  • 2015-05-02 14:28:35, 81.99 K
  • ¸½¼þ 2 : GHZ-8_C13_CDCl3_2015-4-30.fid.rar
  • 2015-05-02 14:28:46, 247.28 K

» ²ÂÄãϲ»¶

» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:

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

׿Խ_ÏÈ·æ

ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)

ºýÍ¿³æ

ÓÅÐã°æÖ÷

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
²éѯ½á¹û£º¹²²éµ½40¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     12-ethyl-5,6,13,14-tetrahydro-2-hdyroxy-3-methoxy-8H-isoquino[2.1-b][2.7]naphthyridin-8-one
C19H20N2O3     ÏàËÆ¶È:68.4%
Canadian Journal of Chemistry          1987          65          2362-2368
8H-Isoquino[2,1-b][2,7]naphthyridin-8-ones: synthesis of the Alangium alkaloids, alangimaridine and alangimarine
Jahangir, Michael A. Brook, David B. MacLean, Herbert L. Holland
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     compound 12a
    ÏàËÆ¶È:66.6%
Journal of Natural Products          2014          77          1021-1030
Spiromastixones A¨CO, Antibacterial Chlorodepsidones from a Deep-Sea-Derived Spiromastix sp. Fungus
Siwen Niu, Dong Liu, Xinxin Hu, Peter Proksch, Zhongzhe Shao, and Wenhan Lin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     austrodimerine
C21H27N3O5     ÏàËÆ¶È:65%
Phytochemistry          1998          47          825-832
Monoterpene alkaloids, iridoids and phenylpropanoid glycosides from Osmanthus austrocaledonica
Rabah Benkrief, Yvonne Ranarivelo, Alexios-Leandros Skaltsounis, Francois Tillequin, Michel Koch, Jacques Pusset, Thierry S¨¦venet
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     compound 4l
C24H34N4O6     ÏàËÆ¶È:65%
European Journal of Organic Chemistry          2011                   4293-4297
Synthesis of Various Chiral 1,2,4-Triazole-Containing -Amino Acids from Aspartic or Glutamic Acids
Anne-Laure Blayo, Fr¨¦d¨¦ric Brunel, Jean Martinez and Jean-Alain Fehrentz
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     ketoheterophyllin A
C20H24O7     ÏàËÆ¶È:65%
Chemical & Pharmaceutical Bulletin          2014          62          1092-1099
Germacranolides and Their Diversity of Eupatorium heterophyllum Collected in P. R. China
Yoshinori Saito, Tomomi Mukai, Yuko Iwamoto, Makiko Baba, Koji Takiguchi, Yasuko Okamoto, Xun Gong, Takayuki Kawahara, Chiaki Kuroda, Motoo Tori
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     ethyl 2,7,7-trimethyl-5-oxo-4-phenyl-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate
C21H25NO3     ÏàËÆ¶È:63.1%
Indian Journal of Chemistry Section B          2008          47B          1084-1090
Hantzsch synthesis of polyhydroquinolines - A simple,efficient and neat protocol
Arumugam,Pandurangan; Perumal,Paramasivan T
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     N,N-Dihexyl-(5-{(E)-2-[5-((E)-2-thiazol-2-yl-vinyl)thiazol-2-yl]vinyl}thiazol-2-yl)amine
C25H34N4S3     ÏàËÆ¶È:63.1%
Zeitschrift f¨¹r Naturforschung B          2007          62          1525-1529
Conjugated Compounds Based on Vinylthiazole Units
H. Meier, F. Nicklas, and R. Petermann
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     dimethyl 6-[(diphenoxyphosphoryl)oxy]-3-hydroxy-4-pentylphthalate
C27H29O9P     ÏàËÆ¶È:63.1%
European Journal of Organic Chemistry          2011                   7140-7147
Olefin-Metathesis-Based Synthesis of Furans by an RCM/Deprotonation/Phosphorylation Sequence and Their Diels¨CAlder Reactions
Bernd Schmidt and Diana Geißler
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     39,42-diacetoxy-5,17,23,35-tetra-tert-butyl-37,38,40,41-tetra-ethoxy-11,29-dinitrocalix[6]arene
C70H86N2O12     ÏàËÆ¶È:63.1%
European Journal of Organic Chemistry          2010                   7005-7011
Microwave-Assisted Synthesis of a Nitro-m-xylylenedioxycalix[6]arene Building Block Functionalized at the Upper Rim
Hitos Gal¨¢n, Javier de Mendoza and Pilar Prados
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     schizanthine I
C19H27NO6     ÏàËÆ¶È:63.1%
Heterocycles          1988          27          1887-1897
Tropane Alkaloids from Schizanthus pinnatus
Gabriel de la Fuente, Mat¨ªas Reina, Orlando Muñoz, Aurelio San Mart¨ªn, and Jean-Pierre Girault
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     12-ethyl-5,6,13,14-tetrahydro-2,3-dimethoxy-8H-isoquino[2.1-b][2.7]naphthyridin-8-one
C20H22N2O3     ÏàËÆ¶È:63.1%
Canadian Journal of Chemistry          1987          65          2362-2368
8H-Isoquino[2,1-b][2,7]naphthyridin-8-ones: synthesis of the Alangium alkaloids, alangimaridine and alangimarine
Jahangir, Michael A. Brook, David B. MacLean, Herbert L. Holland
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     formosusin A
C17H25NO3     ÏàËÆ¶È:63.1%
Bioorganic & Medicinal Chemistry          2014          22          1070-1076
Formosusin A, a novel specific inhibitor of mammalian DNA polymerase ¦Â from the fungus Paecilomyces formosus
Yoshiyuki Mizushina, Hiroe Suzuki-Fukudome, Toshifumi Takeuchi, Kenji Takemoto, Isoko Kuriyama, Hiromi Yoshida, Shinji Kamisuki, Fumio Sugawara
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     [1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl]methyl 3,4-dihydro-4-(4-hydroxyphenyl)-2-oxo-6-propyl-1H-pyrimidine-5-carboxylate
C23H22N6O6     ÏàËÆ¶È:63.1%
Helvetica Chimica Acta          2014          97          375-383
One-Pot Synthesis of (1,2,3-Triazolyl)methyl 3,4-Dihydro-2-oxo-1H-pyrimidine-5-carboxylates as Potentially Active Antimicrobial Agents (pages 375¨C383)
Minoo Dabiri, Peyman Salehi, Mahboubeh Bahramnejad, Majid Koohshari and Atousa Aliahmadi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     2-Amino-5-benzoyl-N-butyl-4-(pyridin-2-yl)-1Hpyrrole-3-carboxamide
C21H22N4O2     ÏàËÆ¶È:63.1%
Chemical Biology & Drug Design          2010          75          277-283
Design of a Versatile Multicomponent Reaction Leading to 2-amino-5-ketoaryl pyrroles
Kan Wang and Alexander Dömling
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     dehydrocannabifuran
    ÏàËÆ¶È:61.9%
Planta Medica          2008          74          267-272
Isolation and Characterization of New Cannabis Constituents from a High Potency Variety
Mohamed M. Radwan, Samir A. Ross, Desmond Slade, Safwat A. Ahmed, Fazila Zulfiqar,Mahmoud A. ElSohly
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     Ethyl 3-Acetoxy-9-methyl-7-(4-nitrophenyl)-6-oxo-7,8-dihydro-6H-dibenzo[b,d]pyran-8-carboxylate
C25H21NO8     ÏàËÆ¶È:60.8%
Synthesis          2012          44          2385−2395
Synthesis of 6H-Dibenzo[b,d]pyran-6-one Derivatives via Coumarin-Fused Cyclohexa-1,3-diene Intermediates
Chen, Chao-Yue; Zhao, Yong-Sheng; Xiang, Chang-Bing; Huang, Zhi-Zhen
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     argutane B
C20H22N2O2     ÏàËÆ¶È:60%
Helvetica Chimica Acta          2007          Vol. 90          2151
Two Novel Monoterpene Alkaloid Dimers from Incarvillea arguta
Jian-Jun Fu, Hui-Zi Jin, Yun-Heng Shen, Wei-Dong Zhang, Wen-Zheng Xu, Qi Zeng, and Shi-Kai Yan
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     lecocarpinolide
    ÏàËÆ¶È:60%
Helvetica Chimica Acta          2005          Vol. 88          160
Novel Sesquiterpenoids from Siegesbeckia orientalis
Ying Xiang, Cheng-Qi Fan, Jian-Min Yue
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
19 .     drypetenone C
C20H22O5     ÏàËÆ¶È:60%
Journal of Natural Products          2001          64          707-709
Chemical Constituents from Drypetes littoralis
×·Çó׿Խ£¬¸ÒΪÏÈ·æ
2Â¥2015-05-02 21:03:19
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
Ïà¹Ø°æ¿éÌø×ª ÎÒÒª¶©ÔÄÂ¥Ö÷ qiaochunlin µÄÖ÷Ìâ¸üÐÂ
×î¾ßÈËÆøÈÈÌûÍÆ¼ö [²é¿´È«²¿] ×÷Õß »Ø/¿´ ×îºó·¢±í
[¿¼ÑÐ] ÍÁľˮÀûר˶276·ÖÇóµ÷¼Á +6 ÎÒÏëÉÏѧ£¡£¡6 2026-04-05 9/450 2026-04-08 17:45 by ËÎС±¦HQ
[¿¼ÑÐ] 331Çóµ÷¼Á +3 luoxin0706. 2026-04-08 3/150 2026-04-08 17:20 by -ÃÔÁË·°¡Â·
[¿¼ÑÐ] »·¾³×¨Ë¶µ÷¼Á +14 »á˵»°µÄÖâ×Ó 2026-04-06 14/700 2026-04-08 16:55 by ŬÁ¦ÏòÉÏ£¬²»¶ÏÅ
[¿¼ÑÐ] Ò»Ö¾Ô¸0703»¯Ñ§ÕÐ61×îÖÕÅÅÃû62»¯Ñ§Çóµ÷¼Á +12 ÕÐ61ÅÅÃû62 2026-04-07 13/650 2026-04-08 15:00 by heqizheng
[¿¼ÑÐ] ²ÄÁϵ÷¼Á +19 Ò»ÑùYWY 2026-04-02 20/1000 2026-04-08 11:02 by ²»³Ôô~µÄ؈
[¿¼ÑÐ] »úеµ÷¼Á +3 zzzbcb 2026-04-07 3/150 2026-04-07 22:19 by hemengdong
[¿¼ÑÐ] 277Çóµ÷¼Á ÊýÒ»104·Ö +9 Æ¿×ÓPZ 2026-04-05 14/700 2026-04-07 17:52 by À¶ÔÆË¼Óê
[¿¼ÑÐ] 325 µ÷¼Á +6 QQСϺ 2026-04-07 6/300 2026-04-07 15:17 by Ccclqqq
[¿¼ÑÐ] 080500Çóµ÷¼Á +12 »ÆÓ 2026-04-06 12/600 2026-04-07 12:41 by upczlm1989
[¿¼ÑÐ] ¹¤¿Æ 22408 267ÇóÍÆ¼ö +4 wanwan00 2026-04-05 5/250 2026-04-06 22:47 by chenzhimin
[¿¼ÑÐ] ²ÄÁÏ334Çóµ÷¼Á +19 Eecho# 2026-04-03 19/950 2026-04-06 08:37 by ССÊ÷2024
[¿¼ÑÐ] Ò»Ö¾Ô¸9²ÄÁÏѧ˶297ÒѹýÁù¼¶Çóµ÷¼ÁÍÆ¼ö +11 adaie 2026-04-04 12/600 2026-04-05 19:04 by À¶ÔÆË¼Óê
[¿¼ÑÐ] ¿¼ÑÐÉúÎïѧ¿¼AÇø211£¬³õÊÔ322£¬¿ÆÄ¿Éú»¯ºÍÉúÎï×ۺϣ¬Çóµ÷¼Á +6 ¡£¡£¡£54 2026-04-03 6/300 2026-04-05 14:54 by JOKER0401
[¿¼ÑÐ] 0832ʳƷ¿ÆÑ§Ó빤³Ìѧ˶282µ÷¼Á +6 ÓãÔÚË®ÖÐÓÎa 2026-04-02 9/450 2026-04-05 11:45 by flysky1234
[¿¼ÑÐ] Ò»Ö¾Ô¸½­ÄÏ´óѧ085501»úе¹¤³Ìר˶326·Ö£¬±¾¿Æ¼Ñľ˹´óѧ +5 ¹ËÈô¸¡Éú 2026-04-03 9/450 2026-04-05 09:57 by 1753564080
[¿¼ÑÐ] 085602µ÷¼Á ³õÊÔ×Ü·Ö335 +12 19123253302 2026-04-04 12/600 2026-04-05 08:08 by 544594351
[¿¼ÑÐ] 341Çóµ÷¼Á +3 Âå¶àÂÞ 2026-04-02 4/200 2026-04-04 21:36 by ÖÇÄÜÖÇ»Û
[¿¼ÑÐ] 280Çóµ÷¼Á +21 ¹¾ààÏþÏþ 2026-04-02 22/1100 2026-04-04 11:12 by Öí»á·É
[¿¼ÑÐ] 22408£¬264Çóµ÷¼Á +3 ywh729 2026-04-03 4/200 2026-04-04 11:04 by ywh729
[¿¼ÑÐ] 283Çóµ÷¼Á +3 jiouuu 2026-04-03 4/200 2026-04-03 13:28 by jiouuu
ÐÅÏ¢Ìáʾ
ÇëÌî´¦ÀíÒâ¼û