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1 .     antirhine
    ÏàËÆ¶È:73.6%
Journal of Natural Products          1989          Vol 52          1107
Alcaoëdes d'Ochrosia alyxioides
Nadia Boughandjioua, Larbi Bengaouer, Francoise Hotellier, Elisabeth Seguin, François Tillequin, Michel Koch, Thierry Sevenet
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     18,19-dihydro-(20R)-antirhine
    ÏàËÆ¶È:73.6%
Phytochemistry          1992          31          2873-2876
Alkaloids from roots of Strychnos potatorum
Georges Massiot, Philippe Thepenier, Marie-Jos¨¦ Jacquier, Louisette Le Men-Olivier, Cl¨¦ment Delaude
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     antirhine
    ÏàËÆ¶È:73.6%
Phytochemistry          1991          30          1697-1700
Matadine, a cytotoxic alkaloid from Strychnos gossweileri
J. Quetin-Leclercq, P. Coucke, C. Delaude, R. Warin, R. Bassleer, L. Angenot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     anthirine
    ÏàËÆ¶È:73.6%
Phytochemistry          1987          26          2839-2846
Alkaloids of Strychnos johnsonii
Georges Massiot,Philippe Th¨¦penier,Marie-Jos¨¦ Jacquier,Louisette Le Men-Olivier,Robert Verpoorte,Cl¨¦ment Delaude
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     compound 6
    ÏàËÆ¶È:68.7%
Planta Medica          1987          53          386-388
Elaboration of the Ethylidene Side Chain in the Synthesis of Indole Alkaloids: Preparation of (¡À)-Deplancheine and its Analogues
Reij a Jokela, Anne Juntunen, and Mauri Lounasmaa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     antirhine
C19H24N2O     ÏàËÆ¶È:68.7%
Journal of Natural Products          1986          Vol 49          1130
Epi-3 Antirhine, Alcaloïde nouveau Extrait de Guettarda heterosepala
C. Kan-Fan, M. H. Brillanceau, H. P. Husson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     compound 3a
C16H19NO2     ÏàËÆ¶È:68.7%
Journal of Heterocyclic Chemistry          2001          38          371-377
Inverse electron-demand 1,3-dipolar cycloaddition reactions of cyclooctyne with pyridinium bis(methoxycarbonyl)methylides
Kiyoshi Matsumoto, Naoto Hayashi, Yukio Ikemi, Mitsuo Toda, Takane Uchida, Kinuyo Aoyama and Yoshihiro Miyakoshi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     6,7,12,12b-tetrahydro-1H-indolo[2,3-a]quinolizin-4-one
C15H14N2O     ÏàËÆ¶È:68.7%
Heterocycles          2004          63          655-661
Syntheses of 1,2,3,4,6,7,12,12b-Octahydroindolo[2,3-a]quinolizine and Harmicine Using a Chiral 1-Allyl-1,2,3,4-tetrahydro-¦Â-carboline as the Starting Material
Takashi Itoh, Michiko Miyazaki, Kazuhiro Nagata, Shigeru Nakamura, and Akio Ohsawa*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     (6S,12bS)-6-(hydroxymethyl)-4-oxo-1,2,3,6,7,12b-hexahydro-12H-indolo[2,3-a]quinolizine
C16H18N2O2     ÏàËÆ¶È:68.7%
European Journal of Organic Chemistry          2011                   3858-3863
Stereocontrolled Generation of Benzo[a]- and Indolo[2,3-a]quinolizidines from (S)-Tryptophanol and (S)-(3,4-Dimethoxyphenyl)alaninol-Derived Lactams
Maria P¨¦rez, Federica Arioli, Gianna Rigacci, Maria M. M. Santos, Arantxa G¨®mez-Esqu¨¦, Carmen Escolano, Pedro Florindo, Carlos Ramos, Joan Bosch and Mercedes Amat
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     20-epi-antirhine
C19H24N2O     ÏàËÆ¶È:68.4%
Journal of Natural Products          1994          Vol 57          287
Indole Alkaloids from Antirhea portoricensis
Bernard Weniger, Robert Anton, Teresa Varea, Jean-Charles Quirion, Jaume Bastida, Ricardo Garcia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
NMR̼Æ×Êý¾Ý¿â--΢Æ×Êý¾Ý--www.nmrdata.com----½âÆ×ºÃ°ïÊÖ
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