²é¿´: 1053  |  »Ø¸´: 3

zhiwu1983

ľ³æ (ÕýʽдÊÖ)

[ÇóÖú] ÇóÖú΢Æ×Êý¾Ý²éѯ

̼Æ×Êý¾ÝÈçÏ£º
1:
144.1,121.7,82.0,71.7,56.6,55.7,54.9,48.6,46.0,43.0,42.1,39.8,37.3,37.1,36.6,36.2,31.8,29.8,29.3,28.6,26.2,25.8,23.2,22.8,21.4,19.9,19.1,12.0
2:
213.2,173.6,143.3,141.7,128.7,119.7,110.1,85.5,79.7,77.4,52.3,52.0,41.4,39.4,39.0,33.7,29.8,26.6,26.4,22.2,20.6,18.3,17.0,11.9,11.6
»Ø¸´´ËÂ¥

» ²ÂÄãϲ»¶

» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:

¼á³Öµ½×îºó
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

ivyasspring

½ð³æ (СÓÐÃûÆø)

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
zhiwu1983: ½ð±Ò+30, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-04-27 16:21:09
µÚÒ»¸ö
1 .     7¦Â-hydroxycholesterol
C27H46O2     ÏàËÆ¶È:76%
Steroids          2005          70          907-912
Synthesis and antifungal activity of oxygenated cholesterol derivatives
Jean Michel Brunel, C¨¦line Loncle, Nicolas Vidal, Michel Dherbomez, Yves Letourneux
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

2 .     compound II
    ÏàËÆ¶È:75%
Russian Journal of Organic Chemistry          2009          45          78-86
Synthesis of nitrogen- and oxygen-containing macrocycles by palladium-catalyzed amination of 3,24-bis(6-chloropyridin-2-yloxy)cholane
A. D. Averin, E. R. Ranyuk, N. V. Lukashev, A. K. Buryak and I. P. Beletskaya
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

3 .     compound 1a
    ÏàËÆ¶È:74.0%
Journal of Asian Natural Products Research          2008          10          521-529
Two new steroidal compounds from starfish Asterias amurensis Lutken
Hong-Wei Liu , Jian-Kuan Li, Da-Wei Zhang, Jing-Chao Zhang, Nai-Li Wang e, Guo-Ping Cai and Xin-Sheng Yao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

4 .     µ¨çÞ-5,22(E)-¶þÏ©-3¦Â,7¦Á-¶þ´¼
C27H44O2     ÏàËÆ¶È:74.0%
Chinese Journal of Marine Drugs          2004          23(1)          1-5
Polyhydroxy sterols from soft coral Dendronephthya gigantea from the South China Sea
LI Guo-qiang, DENG Zhi-wei, GUAN Hua-shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

5 .     3¦Â,7¦Â-Cholest-5-ene-3,7-diol
C27H46O2     ÏàËÆ¶È:74.0%
Steroids          1995          60          290-294
A convenient synthesis of 7¦Á-hydroxycholest-4-en-3-one by the hydroxypropyl-¦Â-cyclodextrin-facilitated cholesterol oxidase oxidation of 3¦Â,7¦Á-cholest-5-ene-3,7-diol
David L. Alexander, Jed F. Fisher
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

6 .     cholesta-5-en-3¦Â,7¦Â-diol
    ÏàËÆ¶È:74.0%
Natural Product Research          2010          24          1518-1522
Isolation and identification of two steroid compounds from Oviductus Ranae
Yongsheng Wang; Lili Wang; Yan Hu; Lantong Zhang; Zhihan Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

7 .     cholest-5-en-3¦Â,7¦Â-diol
    ÏàËÆ¶È:74.0%
Chinese Traditional and Herbal Drugs          1994          25          229-231+265+278
Studies on the Chemical Constituents of the Pilose Antler of Red Deer (Cervus elaphus)
Yang Xiuwei and Bai Yunpeng(Jilin Provincial College of Traditional Chinese Medicine and Materia Medica; Changchun);
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

8 .     7¦Â-hydroxycholesterol
    ÏàËÆ¶È:74.0%
Archives of Pharmacal Research          2010          33          1347-1353
Structural implication in cytotoxic effects of sterols from Sellaginella tamariscina
Eun Mi Roh, Qinglong Jin, Hong-Guang Jin, Ji Eun Shin and Eun Jin Choi, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

9 .     ¦Â-sitosterol
    ÏàËÆ¶È:73.0%
Korean Journal of Pharmacognosy          2004          35(1)          80-87
The Chemical Structures and Their Antioxidant Activity of the Components Isolated from the Heartwood of Hemiptelea davidii
Chang, Bok-Sim; Kwon, Yong-Soo; Kim, Chang-Min
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

10 .     Cholesterol
    ÏàËÆ¶È:72%
Steroids          1993          58          69-73
Synthesis of novel 6-aza-B- and 11-aza-C-homoestranes as antifertility agents
Indra Dwivedy, Ashvani K. Singh, Man Mohan Singh, Suprabhat Ray
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

11 .     6¦Â-Methoxy-3¦Á,5-cyclo-5¦Á-23,24-bisnorcholan-22-carbaldehyde
    ÏàËÆ¶È:70.8%
Steroids          2005          70          551-562
Preparation of (25R)- and (25S)-26-functionalized steroids as tools for biosynthetic studies of cholic acids
Vladimir A. Khripach, Vladimir N. Zhabinskii, Olga V. Konstantinova, Natalya B. Khripach, Alexey V. Antonchick, Andrey P. Antonchick, Bernd Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

12 .     23-Iodo-6¦Â-methoxy-3¦Á,5-cyclo-5¦Á-24-norcholane
C24H39OI     ÏàËÆ¶È:70.8%
Steroids          2005          70          551-562
Preparation of (25R)- and (25S)-26-functionalized steroids as tools for biosynthetic studies of cholic acids
Vladimir A. Khripach, Vladimir N. Zhabinskii, Olga V. Konstantinova, Natalya B. Khripach, Alexey V. Antonchick, Andrey P. Antonchick, Bernd Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

13 .     comopund 1c
    ÏàËÆ¶È:70.8%
Phytochemistry          1990          29          656-659
2¦Á,3¦Á-Dihydroxycativic acid,a diterpenoid from Baccharis petiolata
Jose C. Gianello,Mauricio J. Pestchanker,Carlos E. Tonn,Ming Guo,Oscar S. Giordano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

14 .     (3S,20S)-3-tert-butyldimethylsilyloxy-20-hydroxypregn-5-ene
C27H48O2Si     ÏàËÆ¶È:70.8%
Heterocycles          2005          65          2107-2118
Synthesis of 1-Deoxymaxacalcitol
Tsuyoshi Yamauchi,* Masahiro Kato, Tetsuhiro Mikami, and Yasuo Fujimura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

15 .     24-hydroxy-5¦Â-cholan-3-one
    ÏàËÆ¶È:70.8%
Russian Journal of Organic Chemistry          2011          47          62-65
Copper(i) complexes with polymeric 2,2¡ä-biquinoline-containing ligands as electrocatalysts for selective oxidation of the secondary hydroxy group in 3,24-dihydroxy-5¦Â-cholane with oxygen
T. V. Magdesieva, A. V. Dolganov, G. V. Latyshev, A. V. Yakimanskii and M. Ya. Goikhman, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

16 .     (20R)-24-bromochol-5-en-3¦Â-ol
C24H39BrO     ÏàËÆ¶È:70.8%
Bioorganic & Medicinal Chemistry          2012          20          4064-4081
Substrate analog studies of the ¦Ø-regiospecificity of Mycobacterium tuberculosis cholesterol metabolizing cytochrome P450 enzymes CYP124A1, CYP125A1 and CYP142A1
Jonathan B. Johnston, Arti A. Singh, Anaelle A. Clary, Chiung-Kuan Chen, Patricia Y. Hayes, Sharon Chow, James J. De Voss, Paul R. Ortiz de Montellano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

17 .     3¦Â-hydroxy-cholesta-5-ene
    ÏàËÆ¶È:70.8%
Journal of Shenyang Pharmaceutical University          2012          29          93-97
Studies on the secondary metabolites from the marine-derived fungus Hypocrea virens
LIU Tao; LI Zhan-lin; WANG Yu; TIAN Li; PEI Yue-hu; HUA Hui-ming
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

18 .     cholesterol
    ÏàËÆ¶È:70.3%
Helvetica Chimica Acta          1980          63          1609-1614
Natural Abundance 13C-NMR. of Vitamin D3 Metabolites
Thomas H. Williams, David N. Greeley, Enrico G. Baggiolini, John J. Partridge, Shian-Jan Shiuey, Milan R. Uskokovi¨¦
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

19 .     (24S)-3¦Â-hydroxy-5¦Á-stigmastan-6-one
C29H50O2     ÏàËÆ¶È:70.3%
Steroids          2012          77          91-99
Brassinosteroids and analogs as neuroprotectors: Synthesis and structure¨Cactivity relationships
Jihane Ismaili, Martin Boisvert, Fanny Longpr¨¦, Julie Carange, C¨¦line Le Gall, Maria-Grazia Martinoli, Benoit Daoust
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

20 .     cholest-5-en-1¦Â,4¦Â-diol
C27H46O2     ÏàËÆ¶È:70.3%
Steroids          2013          78          38-43
Cytotoxic cholestane-type and ergostane-type steroids from the aerial parts of Euphorbia altotibetic
Bei-Bei Zhang, Xue-Lian Han, Qian Jiang, Zhi-Xin Liao, Heng-Shan Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-04-27 16:13:58
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

ivyasspring

½ð³æ (СÓÐÃûÆø)

µÚ¶þ¸ö
1 .     ruageanin C
    ÏàËÆ¶È:66.6%
Natural Product Research          2008          22          763-800
13C NMR spectroscopy of D and B, D-ring seco-limonoids of Meliaceae family
T. Narender; T. Khaliq; Shweta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

2 .     ¦¤8¨C143¦Â-acetoxy-2-hydroxy-1-oxo-methylmeliacate
    ÏàËÆ¶È:65.5%
Natural Product Research          2008          22          763-800
13C NMR spectroscopy of D and B, D-ring seco-limonoids of Meliaceae family
T. Narender; T. Khaliq; Shweta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

3 .     3¦Â-acetoxy-1-oxo-¡÷8(30),14(15) methyl meliacate
    ÏàËÆ¶È:65.5%
Journal of the Chemical Society, Perkin Transactions 1          1974                   437-441
13 C nuclear magnetic resonance spectra of some limonoids. Part I. The structure of procerin, an extractive from Carapa procera
David A. H. Taylor
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

4 .     ruageanin B
    ÏàËÆ¶È:62.9%
Natural Product Research          2008          22          763-800
13C NMR spectroscopy of D and B, D-ring seco-limonoids of Meliaceae family
T. Narender; T. Khaliq; Shweta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

5 .     ruageanin C
C29H36O10     ÏàËÆ¶È:62.0%
Journal of Natural Products          1996          59          544-547
Tetranortriterpenoids from Ruagea glabra
Baldwin S. Mootoo and Russel Ramsewak
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

6 .     ¦¤8¨C143¦Â-acetoxy-1-oxo-methylmeliacate (fissinolide)
    ÏàËÆ¶È:62.0%
Natural Product Research          2008          22          763-800
13C NMR spectroscopy of D and B, D-ring seco-limonoids of Meliaceae family
T. Narender; T. Khaliq; Shweta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

7 .     Fissinolide
C29H36O8     ÏàËÆ¶È:62.0%
Phytochemistry          1998          49          1769-1772
limonoids from Khaya senegalensis
Sami A. Khalid, Gerda M. Friedrichsen, Arsalan Kharazmi, Thor G. Theander, Carl E. Olsen, S. Br[oslash]gger Christensen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

8 .     3¦Â-acetoxy-1-oxo-¡÷8(14) methyl meliacate
    ÏàËÆ¶È:62.0%
Journal of the Chemical Society, Perkin Transactions 1          1974                   437-441
13 C nuclear magnetic resonance spectra of some limonoids. Part I. The structure of procerin, an extractive from Carapa procera
David A. H. Taylor
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

9 .     methyl-3¦Â-isobutyroyloxy-2,6-dihydroxy-8¦Á,30¦Á-epoxy-1-oxo-meliacate
    ÏàËÆ¶È:61.5%
Natural Product Research          2008          22          763-800
13C NMR spectroscopy of D and B, D-ring seco-limonoids of Meliaceae family
T. Narender; T. Khaliq; Shweta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

10 .     methyl 2¦Á,3¦Á,4¦Â-trihydroxy-neo-clerodan-15-oate
C21H38O5     ÏàËÆ¶È:60%
Tetrahedron          1995          51          2117-2128
New antifeedant neo-clerodane triol. Semisynthesis and antifeedant activity of neo-clerodane diterpenoids
Julio G. Urones, Pilar Basabe, Anna M. Lithgow, Isidro S. Marcos, Alicia Jim¨¦nez, David D¨ªez, Antonio G¨®mez, A.J.P. White, David J. Williams, Monique S.J. Simmonds, Wally M. Blaney
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

11 .     proceranolide
    ÏàËÆ¶È:59.2%
Natural Product Research          2008          22          763-800
13C NMR spectroscopy of D and B, D-ring seco-limonoids of Meliaceae family
T. Narender; T. Khaliq; Shweta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

12 .     khayasin T
    ÏàËÆ¶È:59.2%
Natural Product Research          2008          22          763-800
13C NMR spectroscopy of D and B, D-ring seco-limonoids of Meliaceae family
T. Narender; T. Khaliq; Shweta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

13 .     methyl angolensate
C27H34O7     ÏàËÆ¶È:59.2%
Heterocycles          2000          53          2233-2240
Novel Rings B,D-Secolimonoids from the Stem Bark of Khaya senegalensis
Samir A. M. Abdelgaleil, Hiroaki Okamura, Tetsuo Iwagawa, Matsumi Doe, and Munehiro Nakatani*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

14 .     5-O-(¦Á-mycarosyl)-platenolide I
C27H44O9     ÏàËÆ¶È:59.2%
The Journal of Antibiotics          1980          33          574-578
ISOLATION AND STRUCTURES OF NITROGEN-FREE PLATENOLIDE GLYCOSIDES II. THE 5-O-(¦Á-MYCAROSYL)- AND 5-O-(3'-DEMETHYL-¦Â-MYCAROSYL)- PLATENOLIDES I AND II
U. GRÄFE, W. SCHADE, W. IHN, G. REINHARDT, K. DORNBERGER, H. THRUM, L. RADICS
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

15 .     swietmanin F
C29H36O10     ÏàËÆ¶È:58.6%
Journal of Natural Products          2009          72          2084-2090
Structurally Diverse Limonoids from the Fruits of Swietenia mahagoni
Bing-Dong Lin, Tao Yuan, Chuan-Rui Zhang, Lei Dong, Bo Zhang, Yan Wu, and Jian-Min Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

16 .     xylocarpin
    ÏàËÆ¶È:58.6%
Natural Product Research          2008          22          763-800
13C NMR spectroscopy of D and B, D-ring seco-limonoids of Meliaceae family
T. Narender; T. Khaliq; Shweta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

17 .     utilin
    ÏàËÆ¶È:56%
Natural Product Research          2008          22          763-800
13C NMR spectroscopy of D and B, D-ring seco-limonoids of Meliaceae family
T. Narender; T. Khaliq; Shweta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

18 .     Methyl 3¦Â-acetoxy-6-hydroxy-1-oxomeliac-14-enoate
C29H36O8     ÏàËÆ¶È:56%
Phytochemistry          1998          49          1769-1772
limonoids from Khaya senegalensis
Sami A. Khalid, Gerda M. Friedrichsen, Arsalan Kharazmi, Thor G. Theander, Carl E. Olsen, S. Br[oslash]gger Christensen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

19 .     N-((1S,4S,4aS,5R,6R,8aS)-5-azido-6-hydroxy-1,6-dimethyl-4-((2S,3R,5S)-3-methyl-5-(prop-1-en-2-yl)-tetrahydrofuran-2-yl)-decahydronaphthalen-1-yl)-4-methylbenzenesulfonamide
C27H40N4O4S     ÏàËÆ¶È:56%
Organic Letters          2004          Vol. 6, No. 7          1123-1126
Total Synthesis of (¡À)-Kalihinol C
Ryan D. White, Gregg F. Keaney, Corin D. Slown, and John L. Wood
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

20 .     Crassarine B
C22H36O5     ÏàËÆ¶È:56%
Marine drugs          2011          9          1955-1968
Bioactive Cembranoids from the Soft Coral Sinularia crassa
Chih-Hua Chao,Kuei-Ju Chou,Chiung-Yao Huang,Zhi-Hong Wen,Chi-Hsin Hsu,Yang-Chang Wu,Chang-Feng Dai and Jyh-Horng Sheu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

21 .     (+)-(1S*,4S*,7R*,10R*)-7-acetoxy-1,4-dihydroxycembra-2E,8(19),11Z-trien-20,10-olide
    ÏàËÆ¶È:56%
Journal of Natural Products          2011          74          2349-2355
Cembranolides from the Leaves of Croton gratissimus
Moses K. Langat, Neil R. Crouch, Peter J. Smith, and Dulcie A. Mulholland
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

22 .     (20R)-cholesta-5,24-diene-2¦Á,3¦Á,4¦Â,21-tetrol 3,21-disulfate
    ÏàËÆ¶È:55.5%
Journal of Natural Products          1998          61          370-374
New Sulfated Polyhydroxysteroids from the Antarctic Ophiuroid Astrotoma agassizii
Alejandro J. Roccatagliata, Marta S. Maier, and Alicia M. Seldes
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

23 .     proceranolide
C27H34O7     ÏàËÆ¶È:55.5%
Chemical & Pharmaceutical Bulletin          1990          38          639-651
Constituents of the Seeds of Swietenia mahagoni JACQ. I. : Isolation, Structures, and 1H- and 13C-Nuclear Magnetic Resonance Signal Assignments of New Tetranortriterpenoids Related to Swietenine and Swietenolide
Shigetoshi KADOTA,Lamek MARPAUNG,Tohru KIKUCHI and Hisao EKIMOTO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

24 .     methyl angolensate
C27H34O7     ÏàËÆ¶È:55.5%
Chemical & Pharmaceutical Bulletin          1990          38          639-651
Constituents of the Seeds of Swietenia mahagoni JACQ. I. : Isolation, Structures, and 1H- and 13C-Nuclear Magnetic Resonance Signal Assignments of New Tetranortriterpenoids Related to Swietenine and Swietenolide
Shigetoshi KADOTA,Lamek MARPAUNG,Tohru KIKUCHI and Hisao EKIMOTO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

25 .     humilinolide C
    ÏàËÆ¶È:55.5%
Natural Product Research          2008          22          763-800
13C NMR spectroscopy of D and B, D-ring seco-limonoids of Meliaceae family
T. Narender; T. Khaliq; Shweta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

26 .     ruageanin D
    ÏàËÆ¶È:55.5%
Natural Product Research          2008          22          763-800
13C NMR spectroscopy of D and B, D-ring seco-limonoids of Meliaceae family
T. Narender; T. Khaliq; Shweta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

27 .     ¦¤14¨C151,3-dioxomethylmeliacate (carapin)
    ÏàËÆ¶È:55.5%
Natural Product Research          2008          22          763-800
13C NMR spectroscopy of D and B, D-ring seco-limonoids of Meliaceae family
T. Narender; T. Khaliq; Shweta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

28 .     2,6-dihydroxy fissinolide
    ÏàËÆ¶È:55.5%
Natural Product Research          2008          22          763-800
13C NMR spectroscopy of D and B, D-ring seco-limonoids of Meliaceae family
T. Narender; T. Khaliq; Shweta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

29 .     seneganolide A
    ÏàËÆ¶È:55.5%
Natural Product Research          2008          22          763-800
13C NMR spectroscopy of D and B, D-ring seco-limonoids of Meliaceae family
T. Narender; T. Khaliq; Shweta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

30 .     methyl-3¦Â-tigloyloxy-2-hydroxy-1-oxo-meliac-8(30)-enate
    ÏàËÆ¶È:55.5%
Natural Product Research          2008          22          763-800
13C NMR spectroscopy of D and B, D-ring seco-limonoids of Meliaceae family
T. Narender; T. Khaliq; Shweta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3Â¥2013-04-27 16:17:55
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
4Â¥2013-04-27 16:24:14
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
Ïà¹Ø°æ¿éÌø×ª ÎÒÒª¶©ÔÄÂ¥Ö÷ zhiwu1983 µÄÖ÷Ìâ¸üÐÂ
×î¾ßÈËÆøÈÈÌûÍÆ¼ö [²é¿´È«²¿] ×÷Õß »Ø/¿´ ×îºó·¢±í
[¿¼ÑÐ] 08¹¤¿Æ 320×Ü·Ö Çóµ÷¼Á +6 À滨çóÍí·ç 2026-03-17 6/300 2026-03-21 03:40 by JourneyLucky
[¿¼ÑÐ] 299Çóµ÷¼Á +6 ¡÷С͸Ã÷* 2026-03-17 6/300 2026-03-21 02:42 by JourneyLucky
[¿¼ÑÐ] 328Çóµ÷¼Á£¬Ó¢ÓïÁù¼¶551£¬ÓпÆÑо­Àú +4 ÉúÎ﹤³Ìµ÷¼Á 2026-03-17 8/400 2026-03-21 02:12 by JourneyLucky
[¿¼ÑÐ] 354Çóµ÷¼Á +5 Tyoumou 2026-03-18 8/400 2026-03-21 00:35 by JourneyLucky
[¿¼ÑÐ] Äϲý´óѧ²ÄÁÏר˶311·ÖÇóµ÷¼Á +5 77chaselx 2026-03-20 5/250 2026-03-20 23:42 by lovewei0727
[¿¼ÑÐ] ¿¼Ñе÷¼ÁÇóÑ§Ð£ÍÆ¼ö +3 ²®ÀÖ29 2026-03-18 5/250 2026-03-20 22:59 by JourneyLucky
[¿¼ÑÐ] 329Çóµ÷¼Á +9 ÏëÉÏѧ߹߹ 2026-03-19 9/450 2026-03-20 22:01 by luoyongfeng
[¿¼ÑÐ] Ò»Ö¾Ô¸ÖÐÄÏ»¯Ñ§£¨0703£©×Ü·Ö337Çóµ÷¼Á +8 niko- 2026-03-19 9/450 2026-03-20 21:57 by luoyongfeng
[¿¼ÑÐ] 260Çóµ÷¼Á +3 ÖìÜÆÁÕ 2026-03-20 3/150 2026-03-20 20:35 by ѧԱ8dgXkO
[¿¼ÑÐ] Ò»Ö¾Ô¸Î÷°²½»Í¨´óѧ ѧ˶ 354Çóµ÷¼Á +3 ÎÒÏëÒª¶ÁÑо¿Éú 2026-03-20 3/150 2026-03-20 20:13 by JourneyLucky
[¿¼ÑÐ] 320Çóµ÷¼Á0856 +3 ²»ÏëÆðÃû×Ö112 2026-03-19 3/150 2026-03-19 22:53 by ѧԱ8dgXkO
[¿¼ÑÐ] ²ÄÁÏ¿¼Ñе÷¼Á +3 xwt¡£ 2026-03-19 3/150 2026-03-19 11:22 by wãåÑôw
[¿¼ÑÐ] Ò»Ö¾Ô¸985£¬±¾¿Æ211£¬0817»¯Ñ§¹¤³ÌÓë¼¼Êõ319Çóµ÷¼Á +10 Liwangman 2026-03-15 10/500 2026-03-19 10:25 by Î޼ʵIJÝÔ­
[¿¼ÑÐ] 0854¿É¿çµ÷¼Á£¬Ò»×÷Ò»ÏîºËÐÄÂÛÎÄÎåÏîרÀû£¬Ê¡¡¢¹ú¼¶Ö¤Êé40+ÊýÒ»Ó¢Ò»287 +8 СÀî0854 2026-03-16 8/400 2026-03-18 14:35 by ²«»÷518
[¿¼ÑÐ] ²ÄÁÏר˶306Ó¢Ò»Êý¶þ +10 z1z2z3879 2026-03-16 13/650 2026-03-18 14:20 by 007_lilei
[¿¼ÑÐ] ÉúÎïѧ071000 329·ÖÇóµ÷¼Á +3 ÎÒ°®ÉúÎïÉúÎﰮΠ2026-03-17 3/150 2026-03-18 10:12 by macy2011
[¿¼ÑÐ] ¿¼ÑÐÇóµ÷¼Á +3 éÙËÌ. 2026-03-17 4/200 2026-03-17 21:43 by ÓÐÖ»ÀêÅ«
[¿¼ÑÐ] ²ÄÁÏר˶326Çóµ÷¼Á +6 Ä«ìÏæ¦Ý· 2026-03-15 7/350 2026-03-17 17:10 by ruiyingmiao
[¿¼ÑÐ] 085601Çóµ÷¼Á +4 Du.11 2026-03-16 4/200 2026-03-17 17:08 by ruiyingmiao
[¿¼ÑÐ] 070300»¯Ñ§Ñ§Ë¶Çóµ÷¼Á +6 Ì«Ïë½ø²½ÁË0608 2026-03-16 6/300 2026-03-16 16:13 by kykm678
ÐÅÏ¢Ìáʾ
ÇëÌî´¦ÀíÒâ¼û