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cyr001: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-04-13 09:32:34
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1 .     tert-butyl indoline-1-carboxylate
    ÏàËÆ¶È:72.7%
Tetrahedron          2014          70          3413-3421
Buchwald¨CHartwig reactions in water using surfactants
Christophe Salom¨¦, Patrick Wagner, Maud Bollenbach, Fr¨¦d¨¦ric Bihel, Jean-Jacques Bourguignon, Martine Schmitt
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     dehydrozingerone
    ÏàËÆ¶È:72.7%
Journal of Food Science          2013          78          M64-M69
In vitro Antifungal Activity of Dehydrozingerone and its Fungitoxic Properties
I. Rahath Kubra, Pushpa S. Murthy, and L. Jagan Mohan Rao
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     4-(3,4-dihydroxy-phenyl)-but-3-en-2-one
    ÏàËÆ¶È:72.7%
Journal of Separation Science          2008          31          1669-1676
Purification and preparation of compounds from an extract of Scutellaria barbata D. Don using preparative parallel high performance liquid chromatography
Yanping Wang, Xingya Xue, Yuansheng Xiao, Feifang Zhang, Qing Xu and Xinmiao Liang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     3,4-dihydroxy-benzalacetone
C10H10O3     ÏàËÆ¶È:72.7%
Chinese Traditional and Herbal Drugs          2011          42          1481-1484
Chemical constituents from rhizome of Matteuccia orientalis
SHAO, Peng, ZHANG, Xue, LI, Chang, SONG, Ying, WANG, Nai-li, YAO, Xin-sheng,
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     (E)-4-(4-hydroxy-3-methoxyphenyl)but-3-en-2-one
    ÏàËÆ¶È:72.7%
Journal of Natural Products          2014          77          2206-2217
Synthesis of Natural and Non-natural Curcuminoids and Their Neuroprotective Activity against Glutamate-Induced Oxidative Stress in HT-22 Cells
Petr Jir¨¢sek, Sabine Amslinger, and Jörg Heilmann
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     dehydrozingerone
    ÏàËÆ¶È:72.7%
International Journal of Molecular Sciences          2014          15          3926−3951
Synthesis of Analogues of Gingerol and Shogaol, the Active Pungent Principles from the Rhizomes of Zingiber officinale and Evaluation of Their Anti-Platelet Aggregation Effects
Hung-Cheng Shih, Ching-Yuh Chern, Ping-Chung Kuo, You-Cheng Wu, Yu-Yi Chan, Yu-Ren Liao, Che-Ming Teng and Tian-Shung Wu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     ¦Ä-(3-methoxy-4-hydroxyphenyl)-¦Ã-valerolactone
    ÏàËÆ¶È:66.6%
Pharmazie          2000          55          364-368
Urinary metabolites of French maritime pine bark extract in humans
K. Grosse D¨¹weler - P. Rohdewald
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     demethoxyencecalin
    ÏàËÆ¶È:66.6%
Bioscience, Biotechnology, and Biochemistry          1996          60          664-665
Antimicrobial Benzopyrans from the Receptacle of Sunflower
Atsushi SATOH, Hisashi UTAMURA, Masato ISHIZUKA, Natsuyo ENDO, Masahisa TSUJI, Hiroyuki NISHIMURA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     compound 10
C12H14O5     ÏàËÆ¶È:66.6%
The Journal of Antibiotics          1990          43          661-667
STROBILURINS F, G AND H, THREE NEW ANTIFUNGAL METABOLITES FROM BOLINEA LUTEA II. STRUCTURE DETERMINATION
ANDREAS FREDENHAGEN, PAUL HUG, HEINRICH H. PETER
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     compound 7
    ÏàËÆ¶È:66.6%
Heterocycles          1997          44          139-142
6-Acetyl-8-hydroxy-2,2-dimethylchromene, an Antioxidant in Sunflower Seeds; Its Isolation and Synthesis and Antioxidant Activity of Its Derivatives
Hideyuki Tsuda, Youichi Ishitani, Yoshiyuki Takemura, Yoshiaki Suzuki, and Tadahiro Kato
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     2,2-dimethyl-6-isopropenyl-2H-pyran
C10H14O     ÏàËÆ¶È:63.6%
Phytochemistry          2002          59          197-203
The monoterpenes of Artemisia tridentata ssp. vaseyana, Artemisia cana ssp. viscidula and Artemisia tridentata ssp. spiciformis
K. Gunawardena, S.B. Rivera, W.W. Epstein
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     (¡À)-methyl 3,4-dihydroxy-5-(2-hydroxy-3-methyl-3-butenyl)benzoate
C13H16O5     ÏàËÆ¶È:63.6%
Journal of Natural Products          2008          71(9)          1538-1543
Benzoic Acid Derivatives from Piper Species and Their Antiparasitic Activity
Ninoska Flores, Ignacio A Jim¨¦nez, Alberto Gim¨¦nez, Grace Ruiz, David Guti¨¦rrez, Genevieve Bourdy, and Isabel L. Bazzocchi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     (¡À)-ethyl 3,4-dihydroxy-5-(2-hydroxy-3-methyl-3-butenyl)benzoate
C14H18O5     ÏàËÆ¶È:63.6%
Journal of Natural Products          2008          71(9)          1538-1543
Benzoic Acid Derivatives from Piper Species and Their Antiparasitic Activity
Ninoska Flores, Ignacio A Jim¨¦nez, Alberto Gim¨¦nez, Grace Ruiz, David Guti¨¦rrez, Genevieve Bourdy, and Isabel L. Bazzocchi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     (¡À)-methyl 3-[2-(acetoxy)-3-methyl-3-butenyl)-4,5-dihydroxybenzoate
C15H18O6     ÏàËÆ¶È:63.6%
Journal of Natural Products          2008          71(9)          1538-1543
Benzoic Acid Derivatives from Piper Species and Their Antiparasitic Activity
Ninoska Flores, Ignacio A Jim¨¦nez, Alberto Gim¨¦nez, Grace Ruiz, David Guti¨¦rrez, Genevieve Bourdy, and Isabel L. Bazzocchi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     methyl 3,4-dihydroxy-5-(3-methyl-2-butenyl)benzoate
C13H16O4     ÏàËÆ¶È:63.6%
Journal of Natural Products          2008          71(9)          1538-1543
Benzoic Acid Derivatives from Piper Species and Their Antiparasitic Activity
Ninoska Flores, Ignacio A Jim¨¦nez, Alberto Gim¨¦nez, Grace Ruiz, David Guti¨¦rrez, Genevieve Bourdy, and Isabel L. Bazzocchi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     4-(3,4-Dihydroxyphenyl)-(E)-3-buten-2-one
    ÏàËÆ¶È:63.6%
Korean Journal of Pharmacognosy          2007          38(2)          164-169
Antioxidative Activities of Phenolic Compounds Isolated from Inonotus obliquus
Kim, Hyoung-Ja; Jin, Chang-Bae; Lee, Yong-Sup
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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