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linjingx: ½ð±Ò+50 2013-02-28 20:10:14
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1 .     ent-stemara-13(14)-en-19-ol
    ÏàËÆ¶È:65%
Phytochemistry          1990          29          3037-3039
Diterpenes from Calceolaria latifolia
Juan A. Garbarino,Aurora Molinari
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     ent-stemar-13(14)-en-19-acetoxy
C22H34O2     ÏàËÆ¶È:65%
Phytochemistry          1990          29          2943-2946
Diterpenes from Calceolaria lepida
Mar¨ªa C. Chamy,Marisa Piovano,Juan A. Garbarino,Cecilia Miranda,Vicente Gambaro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     (+)-2-deoxyoryzalexin S
    ÏàËÆ¶È:65%
Journal of Natural Products          2012          75          1944-1950
Regio- and Diastereoselective Synthesis and X-ray Structure Determination of (+)-2-Deoxyoryzalexin S from (+)-Podocarpic Acid. Structural Nonidentity with Its Nominal Natural Isolated Enantiomer
Francesca Leonelli, Valentina Latini, Andrea Trombetta, Gabriele Bartoli, Francesca Ceccacci, Angela La Bella, Alessio Sferrazza, Doriano Lamba, Luisa M. Migneco, and Rinaldo Marini Bettolo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     4-thia-5¦Â-androstanone
C18H26OS     ÏàËÆ¶È:63.1%
Tetrahedron          2005          61          3691-3696
Shielding effect of thioether C¨CS bond from proton chemical shifts of 4-thia-5¦Á- and 4-thia-5¦Â-androstane-17-ones
Hajime Iwamoto, Takefumi Kawatani, Yoshimasa Fukazawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     compound 4
    ÏàËÆ¶È:63.1%
Tetrahedron          1996          52          2325-2336
Shielding effect of ether C¤RO bond obtained from proton chemical shifts of 4-oxa-5¦Á- and 4-oxa-5¦Â-androstan-17-ones
Yanyan Yang, Takeharu Haino, Shuji Usui, Yoshimasa Fukazawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     ¦Ã-Methoxybutenolide
C21H32O3     ÏàËÆ¶È:61.9%
Journal of Natural Products          1992          Vol 55          256
A New Clerodane-Type Butenolide Diterpene from the Bark of Polyalthia longifolia
Manas Chakrabarty, Amar C. Nath
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     euphadienol
C30H50O     ÏàËÆ¶È:60.8%
Phytochemistry          1995          38          233-236
Three prenylated phenolic benzophenones from Garcinia myrtifolia
Claude Spino, Jitendra Lal, Subramaniam Sotheeswaran, William Aalbersberg
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     (16R)-Ent-3¦Á-hydroxykauran-15-one
C20H32O2     ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          2002          50(6)          808-813
Cytotoxic and Apoptosis-Inducing ent-Kaurane-Type Diterpenoids from the Japanese Liverwort Jungermannia truncata NEES
Fumihiro NAGASHIMA, Masuo KONDOH, Toshinari UEMATSU,Akiko NISHIYAMA£¬Sayaka SAITO,Masao SATO, and Yoshinori ASAKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     (6¦Â)-5(R)-[2-(3-Furanyl)ethyl]-1,1,5,6-tetramethyl-1,2,3,4,5,6,7,8-octahydronaphthalene
C20H30O     ÏàËÆ¶È:60%
Journal of Natural Products          2000          63          1623-1625
Synthesis of 16,18-Dihydroxycleroda-3,13Z-dien-16,15-olide,(+)-16-Hydroxycleroda-3,13Z-dien-16,15-olide, and (-)-Hydroxyhalima-5(10),13-dien-16,15-olide from (+)-Hardwickiic Acid
Paulo M. Imamura, and Marta Costa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     ent-stemar-13(14)-en-17,19-diol
C20H32O2     ÏàËÆ¶È:60%
Phytochemistry          1991          30          3365-3368
Diterpenes from Calceolaria polifolia
Maria C. Chamy, Marisa Piovano, Juan A. Garbarino, Vicente Gambaro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     toonacilidin A
C20H32O2     ÏàËÆ¶È:60%
Planta Medica          2011          77          1617-1622
Limonoids and Diterpenoids from Toona ciliata Roem. var. yunnanensis
Feng Zhang, Shang-Gao Liao, Chuan-Rui Zhang, Xiu-Feng He, Wan-Sheng Chen, Jian-Min Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     kalavelool
    ÏàËÆ¶È:60%
Phytochemistry          1988          27          2265-2268
Lignans and diterpenes of three Aristolochia species
Lucia M.X. Lopes,Vanderlan da S. Bolzani
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     18-hydroxy isopimar-15-ene
C20H32O     ÏàËÆ¶È:60%
Molecules          2011          16          10653-10667
Resin Diterpenes from Austrocedrus chilensis
Ver¨®nica Rachel Olate, Olatz Goikoetxeaundia Usandizaga and Guillermo Schmeda-Hirschmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     14,16-Dinorplakortide Q methyl ester
C20H38O4     ÏàËÆ¶È:60%
Tetrahedron          2005          61          11843-11849
New bioactive cyclic peroxides from the Caribbean marine sponge Plakortis zyggompha
Fabrice Berru¨¦, Olivier P. Thomas, Corinne Funel-Le Bon, Fernando Reyes, Philippe Amade
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     ent-stemar-13(14)-en-19-ol
    ÏàËÆ¶È:59.0%
Phytochemistry          1991          30          3365-3368
Diterpenes from Calceolaria polifolia
Maria C. Chamy, Marisa Piovano, Juan A. Garbarino, Vicente Gambaro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     ent-stemara-13(14)-en-19-acetoxy
C22H34O2     ÏàËÆ¶È:59.0%
Phytochemistry          1990          29          3037-3039
Diterpenes from Calceolaria latifolia
Juan A. Garbarino,Aurora Molinari
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     compound (-)-2
    ÏàËÆ¶È:59.0%
Journal of Natural Products          2012          75          1944-1950
Regio- and Diastereoselective Synthesis and X-ray Structure Determination of (+)-2-Deoxyoryzalexin S from (+)-Podocarpic Acid. Structural Nonidentity with Its Nominal Natural Isolated Enantiomer
Francesca Leonelli, Valentina Latini, Andrea Trombetta, Gabriele Bartoli, Francesca Ceccacci, Angela La Bella, Alessio Sferrazza, Doriano Lamba, Luisa M. Migneco, and Rinaldo Marini Bettolo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     Diacetate
    ÏàËÆ¶È:58.3%
Phytochemistry          1984          23          333-336
Phenolic diterpenoids of podocarpus ferrugineus and other podocarps
Richard C. Cambie, Robert E. Cox, David Sidwell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     laingolide A
C20H35NO3     ÏàËÆ¶È:57.8%
Journal of Natural Products          1999          62          934-936
Madangolide and Laingolide A, Two Novel Macrolides from Lyngbya bouillonii (Cyanobacteria)
D. Klein, J. C. Braekman, D. Daloze, L. Hoffmann, G. Castillo, and V. Demoulin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     5-methyl-19-nor-5¦Â,9¦Â,10¦Â-androstane-3¦Â,17¦Â-diol
C19H32O2     ÏàËÆ¶È:57.8%
Steroids          2002          67          57-70
Analogues of androgen hormones with inverted configuration at carbons 5, 9, and 10
Alexander Kasal, Miloš Budĕš¨ªnsky, Pavel Drašar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     1-methyl-3-(2-thienyl)-l-menthopyrazole
C16H22N2S     ÏàËÆ¶È:57.8%
Journal of Heterocyclic Chemistry          2003          40          773-782
Preparation of 2,6-bis(l-menthopyrzol-3-yl)pyridines and their catalytic activity for asymmetric diels alder reaction
Choji Kashima,Saori Shibata,Hiroyo Yokoyama and Takehiko Nishio
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     (1R,2S,2'S,5¦Á,6S,9R)-5¦Á,9-dimethyl-2¦Â-(1'-methoxyprop-2'-yl)-10,11-dioxatricyclo[7.2.2.01,6]tridecane
C17H30O3     ÏàËÆ¶È:57.8%
Journal of Medicinal Chemistry          1996          39          1885-1897
Structure−Activity Relationships of the Antimalarial Agent Artemisinin. 3. Total Synthesis of (+)-13-Carbaartemisinin and Related Tetra- and Tricyclic Structures
Mitchell A. Avery, Pingchen Fan, Jean M. Karle, Jason D. Bonk, Robert Miller, and D. Keith Goins
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     compound 14
C21H40O     ÏàËÆ¶È:57.8%
Canadian Journal of Chemistry          2004          82          177-184
An iterative approach to three fragments of ionomycin
Claude Spino, Martin Allan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     compound 21
C20H30     ÏàËÆ¶È:57.8%
Australian Journal of Chemistry          1982          35          129-144
A series of new diterpenes from the brown alga Dilophus marginatus (Dictyotaceae)
BN Ravi and RJ Wells
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     14-methoxy-13,14-dihydroanisotom-12E-ene-1-ol
    ÏàËÆ¶È:57.1%
Phytochemistry          2002          59          293-304
Chemosystematic investigations of irregular diterpenes in Anisotome and related New Zealand Apiaceae
Christian Zidorn, Sonja Sturm, John W. Dawson, John W. van Klink,Hermann Stuppner, Nigel B. Perry
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     methyl (-)-(5S,8S,9S,10R)-cleroda-3,13E-dien-15 oate
C21H34O2     ÏàËÆ¶È:57.1%
Phytochemistry          2001          58          1153-1157
Clerodane-type diterpenes from the seed pods of Hymenaea courbaril var. stilbocarpa
Raquel T. Nogueira, George J. Shepherd, Antonio Laverde Jr.,Anita J. Marsaioli, Paulo M. Imamura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     compound 15
    ÏàËÆ¶È:57.1%
Phytochemistry          1999          52          487-493
Nine new clerodane diterpenoids from rhizomes of Solidago altissima
Motoo Tori, Akiko Katto, Masakazu Sono
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     methyl-2¦Â-hydroxy-3,4¦Â-epoxy-neo-clerodan-15-oate
C21H36O4     ÏàËÆ¶È:57.1%
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
29 .     populifolic acid methyl ester
    ÏàËÆ¶È:57.1%
Tetrahedron          1994          50          10791-10802
Ring a functionalized Neo-clerodane diterpenoids from Cistus populifolius
Julio G. Urones, Pilar Basabe, Isidro S. Marcos, Alicia Jim¨¦nez, Anna M. Lithgow, Margarita L¨®pez, Rosalina F. Moro, Antonio G¨®mez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     methyl 2¦Á-hydroxy-3¦Â,4¦Â-epoxy-neo-clerodan-15-oate
    ÏàËÆ¶È:57.1%
Tetrahedron          1994          50          10791-10802
Ring a functionalized Neo-clerodane diterpenoids from Cistus populifolius
Julio G. Urones, Pilar Basabe, Isidro S. Marcos, Alicia Jim¨¦nez, Anna M. Lithgow, Margarita L¨®pez, Rosalina F. Moro, Antonio G¨®mez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     methyl (5R*,8S*,9S*,10R*)-cleroda-3,13-dien-15-oate
    ÏàËÆ¶È:57.1%
Journal of the Brazilian Chemical Society          2002          13          389-391
A New ent-Clerodane Diterpene from Hymenaea courbaril var. altissima
Raquel T. Nogueira, Rosana A. Giacomini, George J. Shepherd and Paulo M. Imamura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     compound 25a
    ÏàËÆ¶È:56.5%
Phytochemistry          1990          29          3173-3187
Diterpenes and other constituents from Relhania species
F. Tsichritzis,J. Jakupovic
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     (+)-9-deoxybuxandonine
C24H41N     ÏàËÆ¶È:56.5%
Tetrahedron          1992          48          3577-3584
Novel triterpenoids from the roots of Buxus papillosa
Atta-ur-Rahman, Nasir Habib, S. Erfan Asif, Ali Safdar, Iqbal Zahida, M.Iqbal Choudhary, Jon Clardy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     leoheteronin C
C20H28O4     ÏàËÆ¶È:55%
Chemical & Pharmaceutical Bulletin          2005          53(8)          938-941
New Labdane-Type Diterpenoids from Leonurus heterophyllus SW.
Phan Minh GIANG,Phan Tong SON,Katsuyoshi MATSUNAMI,and Hideaki OTSUKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     (-)-(5R,8S,9S,10R)-cleroda-3,13E-dien-15 oic acid
C20H32O2     ÏàËÆ¶È:55%
Phytochemistry          2001          58          1153-1157
Clerodane-type diterpenes from the seed pods of Hymenaea courbaril var. stilbocarpa
Raquel T. Nogueira, George J. Shepherd, Antonio Laverde Jr.,Anita J. Marsaioli, Paulo M. Imamura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     dunniana acid B
C20H32O4     ÏàËÆ¶È:55%
Journal of Natural Products          2002          65          392-394
Two New Ring A-Rearranged Clerodane Diterpenes, Dunniana Acids A and B,from Clausena dunniana
Hong-Ping He, Yue-Mao Shen, Xin Hong, Yi-Bin Zhao, Jun Zhou, and Xiao-Jiang Hao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     (4a¦Á,6¦Â,8a¦Â)-1-hydroxymethyl-5(R)-[2-(2,5-dihydro-5-hydroxy-2-oxo-4-furanyl)ethyl]-5,6,8a-trimethyl-3,4,-4a,5,6,7,8,8a-octahydronaphthalene
C20H30O4     ÏàËÆ¶È:55%
Journal of Natural Products          2000          63          1623-1625
Synthesis of 16,18-Dihydroxycleroda-3,13Z-dien-16,15-olide,(+)-16-Hydroxycleroda-3,13Z-dien-16,15-olide, and (-)-Hydroxyhalima-5(10),13-dien-16,15-olide from (+)-Hardwickiic Acid
Paulo M. Imamura, and Marta Costa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     (4a¦Á,6¦Â,8a¦Â)-5(R)-[2-(2,5-Dihydro-5-hydroxy-2-oxo-4-furanyl)ethyl]-1,5,6,8a-tetramethyl-3,4,4a,5,6,7,8,8a-octahydronaphthalene
C20H30O3     ÏàËÆ¶È:55%
Journal of Natural Products          2000          63          1623-1625
Synthesis of 16,18-Dihydroxycleroda-3,13Z-dien-16,15-olide,(+)-16-Hydroxycleroda-3,13Z-dien-16,15-olide, and (-)-Hydroxyhalima-5(10),13-dien-16,15-olide from (+)-Hardwickiic Acid
Paulo M. Imamura, and Marta Costa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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