±±¾©Ê¯ÓÍ»¯¹¤Ñ§Ôº2026ÄêÑо¿ÉúÕÐÉú½ÓÊÕµ÷¼Á¹«¸æ
²é¿´: 311  |  »Ø¸´: 1

xicaicai1988

½ð³æ (СÓÐÃûÆø)

[ÇóÖú] 11 ÒÑÓÐ1È˲ÎÓë

̼Æ×Êý¾Ý£º66.357, 108.672, 121.431, 121.998, 123.222, 128.920
»Ø¸´´ËÂ¥

» ²ÂÄãϲ»¶

Luck is what happens when preparation meets opportunity
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

·çÐÐÕß007

ÖÁ×ðľ³æ (ÖøÃûдÊÖ)

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
²éѯ½á¹û£º¹²²éµ½127¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     compound 2a
    ÏàËÆ¶È:71.4%
Magnetic Resonance in Chemistry          1988          26          8-13
13C and 15N NMR studies of 1,2-benzisoxazole 2-oxides, 1,2-benzisoxazoles and 2-hydroxyaryl ketoximes
Petros G. Tsoungas and Bruce F. De Costa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     compound 3
    ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          1984          32          2622-2627
O-Methylation Effect on the Carbon-13 Nuclear Magnetic Resonance Signals of ortho-Disubstituted Phenols and Its Application to Structure Determination of New Phthalides from Aspergillus silvaticus
MASAO FUJITA,MIKIKO YAMADA,SHOICHI NAKAJIMA,KENICHI KAWAI and MASAHIRO NAGAI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     compound 2b
    ÏàËÆ¶È:62.5%
Magnetic Resonance in Chemistry          1988          26          8-13
13C and 15N NMR studies of 1,2-benzisoxazole 2-oxides, 1,2-benzisoxazoles and 2-hydroxyaryl ketoximes
Petros G. Tsoungas and Bruce F. De Costa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     compound 11n
    ÏàËÆ¶È:57.1%
Magnetic Resonance in Chemistry          1988          26          134-151
Effect of N-substituents on the 13C NMR parameters of azoles
Mikael Begtrup, Jos¨¦ Elguero, Robert Faure, Pelayo Camps, Carmen Estop¨¢, Dušan Ilavsky, Alain Fruchier, Claude Marzin and Javier de Mendoza
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     perimidine-2-sulphonic acid
    ÏàËÆ¶È:57.1%
Magnetic Resonance in Chemistry          1988          26          191-196
13C and 1H NMR studies of structure and tautomerism in some perimidines
P. D. Woodgate, J. M. Herbert and W. A. Denny
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     compound 2a
C11H10N2O2     ÏàËÆ¶È:55.5%
Journal of Heterocyclic Chemistry          2000          37          15-24
Synthesis and nuclear magnetic resonance spectroscopic studies of 1-arylpyrroles
Chang Kiu Lee, Jung Ho Jun and Ji Sook Yu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     1-(1,2,3-triazol-4-yl)benzimidazolone
C9H7N5O     ÏàËÆ¶È:55.5%
Journal of Heterocyclic Chemistry          2000          37          1169-1176
1-(1,2,3-triazol-4-yl)-benzimidazolones, a new series of heterocyclic derivatives
Lucia Bertelli, Giuliana Biagi, Vincenzo Calderone, Irene Giorgi, Oreste Livi, Valerio Scartoni and Pier Luigi Barili
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     compound 3f
C18H15Cl2N     ÏàËÆ¶È:55.5%
Tetrahedron Letters          2001          42          6595-6597
One-pot synthesis of pyrrole derivatives from (E)-1,4-diaryl-2-butene-1,4-diones
H Surya Prakash Rao, S Jothilingam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     1-methoxyindole
    ÏàËÆ¶È:55.5%
Bioorganic & Medicinal Chemistry          2014          22          856-864
Synthesis and anti-inflammatory activity of indole glucosinolates
Quan V. Vo, Craige Trenerry, Simone Rochfort, Jenny Wadeson, Carolina Leyton, Andrew B. Hughes
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     compound 11p
    ÏàËÆ¶È:55.5%
Magnetic Resonance in Chemistry          1988          26          134-151
Effect of N-substituents on the 13C NMR parameters of azoles
Mikael Begtrup, Jos¨¦ Elguero, Robert Faure, Pelayo Camps, Carmen Estop¨¢, Dušan Ilavsky, Alain Fruchier, Claude Marzin and Javier de Mendoza
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     methyl 1-methoxyindole-3-carboxylate
C11H11NO3     ÏàËÆ¶È:54.5%
Phytochemistry          1998          49          1959-1965
Macrocyclic bisbibenzyls in cultured cells of the liverwort, Heteroscyphus planus
Kensuke Nabet¦Á, Shinichi Ohkubo, Reiko Hozumi, Kenji Katoh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     2-(2-bromoprop-2-en-1-yl)-1-methoxy-1H-indole
C12H12NBrO     ÏàËÆ¶È:54.5%
Heterocycles          2006          68          2349-2356
Regioselective Reaction of 2-Indolylcyanocuprates with Electrophiles
Minoru Ishikura,* Reina Uemura, Koji Yamada, and Reiko Yanada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     3-(2-nitrovinyl)-1-methoxyindole
C11H10O3N2     ÏàËÆ¶È:54.5%
Bioorganic & Medicinal Chemistry          2014          22          856-864
Synthesis and anti-inflammatory activity of indole glucosinolates
Quan V. Vo, Craige Trenerry, Simone Rochfort, Jenny Wadeson, Carolina Leyton, Andrew B. Hughes
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     4-bromopyrrol-2-yl trichloromethyl ketone
C6H3NOCl3Br     ÏàËÆ¶È:50%
Journal of Natural Products          2006          69(1)          125-127
Isolation and Synthesis of 4-Bromopyrrole-2-carboxyarginine and 4-Bromopyrrole-2-carboxy-N(¦Å)-lysine from the Marine Sponge Stylissa caribica
Achim Grube, Ellen Lichte, and Matthias Kck
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     2,3-dibromo-4,5-dihydroxybenzyl methyl sulfoxide
C8H8O3Br2S     ÏàËÆ¶È:50%
Journal of Natural Products          2004          67          1032-1035
Bromophenol Derivatives from the Red Alga Rhodomela confervoides
Jielu Zhao, Xiao Fan, Sujuan Wang, Shuai Li, Suqin Shang, Yongchun Yang, Nianjun Xu, Yang L, and Jiangong Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     dictamnine
C12H9NO2     ÏàËÆ¶È:50%
Chemistry of Natural Compounds          1996          32          386-512
ALKALOIDS. PLANTS, STRUCTURES, PROPERTIES CHAPTER , continued
R. Shakirov, M. V. Telezhenetskaya, I. A. Bessonova,S. F. Aripova, I. A. Israilov, M. N. Suitankhodzhaev,V. I. Vinogradova, V. I. Akhmedzhanova, T. S. Tulyaganov,B. T. Salimov, and V. A. Tel'nov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     [1.1]-(N,N'',N: N''')-2,2'-Bipyrrolophane
    ÏàËÆ¶È:50%
Helvetica Chimica Acta          1980          63          1190-1197
On the Use of N, N'-Dipyrrolylmethane in Heterocyclic Synthesis. Dipyrrolo [1,2c:2¡ä, 1¡äe]-2 H-imidazole and its Aromatic Anion
Ulrich Burger, Francine Dreier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     1-methoxy-3-indolecarbaldehyde
    ÏàËÆ¶È:50%
China Journal of Chinese Materia Medica          2007          32          688-691
Studies on chemical constituents in root of Isatis indigotica
ZUO Li, LI Jianbei, XU Jing, YANG Jingzhi, ZHANG Dongming, TONG Yongling
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     diosgenone
    ÏàËÆ¶È:50%
China Journal of Chinese Materia Medica          2002          27          123-125
Studies on Chemical Constituents of Two Plants from Costus
QIAO Chunfeng, Li Qiuwen, DONG Hui, Xu Luoshan, WANG Zhengtao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     2,7-dibromocarbazole
C12H7NBr2     ÏàËÆ¶È:50%
Phytochemistry          1999          52          537-540
Maculalactone L and three halogenated carbazole alkaloids from Kyrtuthrix maculans
Sung-Chi Lee, Gray A. Williams, Geoffrey D. Brown
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     aldisin
C8H8N2O2     ÏàËÆ¶È:50%
Journal of Natural Products          1985          Vol 48          47-53
Marine Natural Products: Pyrrololactams from Several Sponges
Francis J. Schmitz, Sarath P. Gunasekera, Vijai Lakshmi, L. M. V. Tillekeratne
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     3-Bromo-2-methylthiophene
    ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          2011          59(6)          797-798
Practical Preparation of Ethyl 2-Methylthiophene-3-carboxylate
Masakazu KOGAMI and Nobuhide WATANABE
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
½Å̤ʵµØ£¬·ÜÁ¦Ò»²«£¬Ô¹¬ÕÛ¹ð
2Â¥2014-12-25 17:14:15
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
Ïà¹Ø°æ¿éÌø×ª ÎÒÒª¶©ÔÄÂ¥Ö÷ xicaicai1988 µÄÖ÷Ìâ¸üÐÂ
×î¾ßÈËÆøÈÈÌûÍÆ¼ö [²é¿´È«²¿] ×÷Õß »Ø/¿´ ×îºó·¢±í
[¿¼ÑÐ] Çóµ÷¼Á +3 ũҵ¹¤³ÌÓëÐÅÏ¢¼ 2026-04-04 3/150 2026-04-04 12:19 by Éá¶øºóµÃ
[¿¼ÑÐ] Ò»Ö¾Ô¸Äϲý´óѧ324Çóµ÷¼Á +9 hanamiko 2026-03-30 9/450 2026-04-04 11:04 by Öí»á·É
[¿¼ÑÐ] 316Çóµ÷¼Á +5 Ä«³½_Orion926 2026-04-04 5/250 2026-04-04 08:46 by jp9609
[¿¼ÑÐ] Çóµ÷¼Á +3 wos666 2026-04-03 3/150 2026-04-04 05:16 by gswylq
[¿¼ÑÐ] »¯Ñ§µ÷¼ÁÇóÖú +6 LULONG1 2026-04-03 6/300 2026-04-03 23:13 by qzxyhcsy
[¿¼ÑÐ] ¿¼ÑÐÇóµ÷¼Á +3 ľÐÄÏë¼ÌÐøÉîÔì 2026-04-03 3/150 2026-04-03 21:56 by à£à£à£0119
[¿¼ÑÐ] Çóµ÷¼Á +3 wos666 2026-04-03 3/150 2026-04-03 21:36 by lbsjt
[¿¼ÑÐ] 315Çóµ÷¼Á +6 ˳Àí³ÉÕÅ 2026-04-03 8/400 2026-04-03 14:04 by °ÙÁéͯ888
[¿¼ÑÐ] Çóµ÷¼Á +3 ÐÄÏëÊÂ³É¿É 2026-04-03 3/150 2026-04-03 11:22 by wangjy2002
[¿¼ÑÐ] ÉúÎïѧÇóµ÷¼Á +3 15064154688 2026-04-03 3/150 2026-04-03 10:28 by macy2011
[¿¼ÑÐ] 295Çóµ÷¼Á +7 Ô¸ÂÃ;ÓÀԶ̹Ȼ 2026-04-02 7/350 2026-04-03 08:22 by fangshan711
[¿¼ÑÐ] Ò»Ö¾Ô¸Î人Àí¹¤0856£¬³õÊÔ334 +3 26¿¼ÑвÄÁÏ 2026-04-02 3/150 2026-04-02 21:22 by dongzh2009
[¿¼ÑÐ] 293Çóµ÷¼Á +4 çæçæÀÖ 2026-04-02 4/200 2026-04-02 20:10 by 6781022
[¿¼ÑÐ] µ÷¼Á +3 ºÃºÃ¶ÁÊé¡£ 2026-04-01 6/300 2026-04-02 15:49 by liumengping
[¿¼ÑÐ] 286·Öµ÷¼Á +20 Faune 2026-03-30 22/1100 2026-04-02 13:24 by clyblh
[¿¼ÑÐ] 266Çóµ÷¼Á +4 ѧԱ97LZgn 2026-04-02 4/200 2026-04-02 09:52 by yulian1987
[¿¼ÑÐ] 11408 321·ÖÇóµ÷¼Á +3 huchun12138 2026-03-30 4/200 2026-04-01 22:48 by guanxin1001
[¿¼ÑÐ] 304Çóµ÷¼Á +12 ËØÄê¼ÀÓï 2026-03-31 15/750 2026-04-01 22:41 by peike
[¿¼ÑÐ] 085602»¯Ñ§¹¤³Ì268·Ö¶×µ÷¼Á +8 ÔÂÕÕ»¨ÁÖ¡£ 2026-04-01 8/400 2026-04-01 22:08 by Î޼ʵIJÝÔ­
[¿¼ÑÐ] 070300»¯Ñ§354Çóµ÷¼Á +15 101´ÎÏ£Íû 2026-03-28 15/750 2026-03-31 17:58 by jp9609
ÐÅÏ¢Ìáʾ
ÇëÌî´¦ÀíÒâ¼û