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fuxueteng: ½ð±Ò+8, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-01-29 14:17:32
1 .     6-epi-¦Â-cubebene
C15H24     ÏàËÆ¶È:56.2%
Phytochemistry          2002          59          805-810
epi-Cubebanes from Solidago canadensis
Adeleke A. Kasali, Olusegun Ekundayo, Claudia Paul, Wilfried A. König
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     3¦Â-hydroxyartemisinin
C15H22O6     ÏàËÆ¶È:56.2%
Journal of Natural Products          2002          65          1693-1695
Microbial Metabolism of Artemisinin by Mucor polymorphosporus and Aspergillus niger
Ji-Xun Zhan,Yuan-Xing Zhang,Hong-Zhu Guo, Jian Han, Li-Li Ning,and De-An Guo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     9¦Â,13-epoxy-14,15,16,20-tetranorlabdane
    ÏàËÆ¶È:56.2%
Helvetica Chimica Acta          1980          63          1932-1946
Stereochemistry-Odor Relationships in Enantiomeric Ambergris Fragrances
G¨¹nther Ohloff, Christian Vial, Hans Richard Wolf, Kurt Job, Elise J¨¦gou, Judith Polonsky, Edgar Lederer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     ent-9¦Â,13-epoxy-14,15,16,20-tetranorlabdane
    ÏàËÆ¶È:56.2%
Helvetica Chimica Acta          1980          63          1932-1946
Stereochemistry-Odor Relationships in Enantiomeric Ambergris Fragrances
G¨¹nther Ohloff, Christian Vial, Hans Richard Wolf, Kurt Job, Elise J¨¦gou, Judith Polonsky, Edgar Lederer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     compound 3a
    ÏàËÆ¶È:56.2%
Natural Product Research          1995          7          43-46
A Simple and Efficient Approach for the Synthesis of a 1,2,4-Trioxane related to Artemisinin
Silvia N. Huber; Mirta P. Mischne
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     homalomenol C
C15H26O3     ÏàËÆ¶È:56.2%
China Journal of Chinese Materia Medica          2003          28          342-344
Studies on the Constituents in Rhizome of Homalomena occuta
HU Yongmei, YANG Zhonglin, YE Wencai, CHONG Qihou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     kessane
    ÏàËÆ¶È:56.2%
Phytochemistry          1993          33          857-862
Cis-dihydroagarofuran from Prostanthera sp. aff. ovalifolia
Ian A. Southwell, David J. Tucker
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     1¦Â-acetoxy-9¦Á-cinnamoyloxy-¦Â-dihydroagarofuran
C26H34O5     ÏàËÆ¶È:56.2%
Phytochemistry          1991          30          271-273
Sesquiterpenoids from Celastrus gemmatus
Yong Q. Tu, De Z. Wang, Hong J. Zhang, Zhou Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     (2S,4aS,8aR)-1-(2-hydroxyethyl)-octahydro-2,7,7-trimethyl-2H-1,4a-(epoxymethano)naphthalen-2-ol
C16H28O3     ÏàËÆ¶È:56.2%
Chemistry & Biodiversity          2010          7          421-439
Bioactive Compounds with Added Value Prepared from Terpenes Contained in Solid Wastes from the Olive Oil Industry
Andres Parra, Pilar E. Lopez and Andres Garcia-Granados
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     Senecrassidiol
C15H24O2     ÏàËÆ¶È:56.2%
Phytochemistry          1981          20          469-472
Sesquiterpenes from three Senecio species
Ferdinand Bohlmann, J¨¹rgen Ziesche
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     compound 24
    ÏàËÆ¶È:56.2%
Tetrahedron Letters          2002          43          6975-6978
Towards a total synthesis of guanacastepene A: construction of fully functionalized AB and BC ring segments
Goverdhan Mehta, Jayant D Umarye, Vanessa Gagliardini
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     isocaespitol
    ÏàËÆ¶È:56.2%
Tetrahedron letters          1979          20          2719-2722
Carbon-13 NMR application to Laurencia polyhalogenated sesquiterpenes
A.G. Gonz¨¢lez, J.D. Mart¨ªn, V.S. Mart¨ªn, M. Norte
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     9¦Á-Hydroxyclovan-2-one
C15H24O2     ÏàËÆ¶È:56.2%
Bulletin of the Chemical Society of Japan          2011          84          119-121
Rumphellclovane B, a Novel Clovane Analogue from the Gorgonian Coral Rumphella antipathies
Hsu-Ming Chung, Tsong-Long Hwang, Yung-Husan Chen, Jui-Hsin Su, Mei-Chin Lu, Jih-Jung Chen, Jan-Jung Li, Lee-Shing Fang, Wei-Hsien Wang, Ping-Jyun Sung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     compound 4e
C30H54Pd2     ÏàËÆ¶È:56.2%
European Journal of Organic Chemistry          2012                   1945-1952
Development of the First Menthane-Based Chiral Bis(¦Ð-allylpalladium) Catalysis: Asymmetric Allylation of Imines
Rodney A. Fernandes and Dipali A. Chaudhari
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     (1R,5S,7R,8R,10R)-2-hydroxy-1,8-dimethyl-4-oxo-11-oxatricyclo-[6.2.1.0(5,10)]undec-3-yl acetate
C14H20O5     ÏàËÆ¶È:56.2%
Russian Journal of Organic Chemistry          2010          46          226-235
Reactions of stereocontrolled intramolecular carbocyclization of levoglucosenone adduct with isoprene
B. T. Sharipov, O. Yu. Krasnoslobodtseva, L. V. Spirikhin and F. A. Valeev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     compound IIIa
    ÏàËÆ¶È:56.2%
Russian Journal of Organic Chemistry          2001          37          9-14
Peroxyacetylenic Derivatives of Menthol
E. A. Dikusar, N. G. Kozlov, V. M. Zelenkovskii, E. V. Vashkevich and A. P. Yuvchenko, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     compound 7
    ÏàËÆ¶È:56.2%
Magnetic Resonance in Chemistry          1991          29          323-326
13C NMR chemical shift assignments for some n-butylthiomethylene ketones
Angel Guerrero, Alfredo Parrilla and Francisco J. Sanchez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     3,6,7-tris-epi-Helifolene
    ÏàËÆ¶È:56.2%
Flavour and Fragrance Journal          1999          14          121-130
Constituents of the essential oil of Pulicaria gnaphalodes (Vent.) Boiss. from Iran
Peter Weyerstahl, Helga Marschall, Hans-Christian Wahlburg, Christian Christiansen, Abdolhossein Rustaiyan and Fatemeh Mirdjalili
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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