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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½1299¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |

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