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»¯ºÏÎï3 ²éѯ½á¹û£º¹²²éµ½6681¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . methyl (23¦Á,25R)-3,4-seco-9¦ÂH-lanosta-4(28),7-dien-26,23-olid-3-oate C31H48O4 ÏàËÆ¶È:78.1% Journal of Natural Products 2002 65 1657-1659 Triterpenoid Constituents Isolated from the Bark of Abies sachalinensis Shun-ichi Wada, Akira Iida, and Reiko Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (23¦Á,25R)-3,4-seco-9¦ÂH-lanosta-4(28),7-dien-26,23-olid-3-oic acid C30H46O4 ÏàËÆ¶È:75% Journal of Natural Products 2002 65 1657-1659 Triterpenoid Constituents Isolated from the Bark of Abies sachalinensis Shun-ichi Wada, Akira Iida, and Reiko Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 28-hydroxy-3-epicalenduladiol C30H50O3 ÏàËÆ¶È:68.7% Journal of Natural Products 2009 72 1045-1048 Triterpenoids and a Lignan from the Aerial Parts of Maytenus apurimacensis Nabil E. J. Vazdekis, Haydee Ch¨¢vez, Ana Est¨¦vez-Braun, and ¨¢ngel G. Ravelo Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . dimethyl Ester of 2-cyano-2,3-seco-lup-20(29)-en-3,28-dioic acid C32H48NO4 ÏàËÆ¶È:68.7% Chemistry of Natural Compounds 2008 44 606-611 SYNTHESIS OF LUPANE AND 19¦Â,28-EPOXY-18¦Á-OLEANANE 2,3-seco-DERIVATIVES BASED ON BETULIN I. A. Tolmacheva, A. V. Nazarov, O. A. Maiorova, and V. V. Grishko Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Rhoiptelic acid C30H48O3 ÏàËÆ¶È:68.7% Phytochemistry 1995 40 219-224 A rearranged ursane triterpenoid from Rhoiptelea chiliantha Zhi-Hong Jiang, Rong-Han Zhou, Kazuo Masuda, Hiroyuki Ageta Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Rhoiptelic acid methyl ester ÏàËÆ¶È:68.7% Phytochemistry 1995 40 219-224 A rearranged ursane triterpenoid from Rhoiptelea chiliantha Zhi-Hong Jiang, Rong-Han Zhou, Kazuo Masuda, Hiroyuki Ageta Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (-)-(24R)-tirucalla-8,25-diene-3¦Â,24-diol C30H50O2 ÏàËÆ¶È:65.6% Journal of Natural Products 2009 72 1620-1626 Chemical Constituents of the Roots of Euphorbia micractina Wendong Xu, Chenggen Zhu, Wei Cheng, Xiaona Fan, Xiaoguang Chen, Sen Yang, Ying Guo, Fei Ye, and Jiangong Shi Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 3¦Â-hydroxy-29-norcycloart-24-one C29H48O2 ÏàËÆ¶È:65.6% Chemical & Pharmaceutical Bulletin 2001 49(2) 183-187 Triterpenes and Lignans from Artemisia caruifolia and Their Cytotoxic Effects on Meth-A and LLC Tumor Cell Lines Chao-mei MA, Norio NAKAMURA, Byung Sun MIN, and Masao HATTORI Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . seco-coccinic acid E C30H48O3 ÏàËÆ¶È:65.6% Journal of Natural Products 2008 71(6) 990-994 Lanostane-Type Triterpenoids from the Roots of Kadsura coccinea Nan Wang, Zhanlin Li, Dandan Song, Wei Li, Hongwei Fu,Kazuo Koike, Yuehu Pei, Yongkui Jing, and Huiming Hua Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . queretaroic acid C30H48O4 ÏàËÆ¶È:65.6% Journal of Natural Products 1998 61 456-460 New Triterpenes from Machaerocereus eruca Yang Ye, Kaoru Kinoshita, Kiyotaka Koyama, Kunio Takahashi, Norio Kondo, and Hiroshi Yuasa Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 3¦Á-hydroxy-7-oxolanosta-8,24-dien-26,23R-olide acetylation ÏàËÆ¶È:65.6% Planta Medica 2000 66 163-168 Three New Lanostane-Type Triterpene Lactones from the Stem Bark of Abies mariesii Reiko Tanaka,Hitoshi Aoki,Tomoshi Mizota,Shun-ich Wada,Shunyo Matsunaga ,Harukuni Tokuda,Hoyoku Nishino Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 29-nor-cycloartan-23-ene-3,25-diol C29H48O2 ÏàËÆ¶È:65.6% Planta Medica 1988 54 40-41 New Cycloartenol Derivatives from Aglaia roxburghiana S. P. Vishnoi, A. Shoeb, and R. S. Kapil Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 4b ÏàËÆ¶È:65.6% Chemical & Pharmaceutical Bulletin 1989 37 1673-1675 FERN CONSTITUENTS : THREE FERNENOIC ACIDS AND ONE ADIANENOIC ACID ISOLATED FROM RHIZOMES OF MICROSORIUM BRACHYLEPIS AND M. NORMALE Kazuo MASUDA,Rumiko KAMAYA,Susumu IKEGAMI,Yukio IKESHIMA and Hiroyuki AGETA Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . methyl ester of 2-cyano-2,3-seco-19¦Â,28-epoxy-18¦Á-oleanan-3-oic acid C31H49NO3 ÏàËÆ¶È:65.6% Chemistry of Natural Compounds 2008 44 606-611 SYNTHESIS OF LUPANE AND 19¦Â,28-EPOXY-18¦Á-OLEANANE 2,3-seco-DERIVATIVES BASED ON BETULIN I. A. Tolmacheva, A. V. Nazarov, O. A. Maiorova, and V. V. Grishko Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (24S)-5¦Á-lanost-9(11)-ene-3¦Â,24,25-triol C30H52O3 ÏàËÆ¶È:65.6% Acta Botanica Sinica 2004 46 1002-1008 Terpenoids and Phenols from Taiwania flousiana XIANG Ying, YANG Sheng-Ping, ZHAN Zha-Jun, YUE Jian-Min Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 2¦Á,3¦Á,19¦Á-trihydroxy-olean-12-en-28-oic acid ÏàËÆ¶È:65.6% Phytochemistry 2000 54 751-756 Triterpene saponins and iridoid glucosides from Galium rivale Salvatore de Rosa, Carmine Iodice, Maya Mitova, Nedjalka Handjieva, Simeon Popov, Mincho Anchev Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . acetonide of 2¦Á,3¦Á-dihydroxy-urs-12,19-dien-28-oic acid ÏàËÆ¶È:65.6% Acta Pharmaceutica Sinica 2001 Vol 36 38-41 CHEMICAL CONSTITUENTS FROM THE ROOT OF RUBUS CHROOSEPALUS LIU Rong; DING Li sheng; CHEN Neng yu; WANG Ming kui Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . wilforol ÏàËÆ¶È:65.6% Acta Pharmaceutica Sinica 1999 Vol 34 210-213 THE TRITERPENOIDS OF TRIPTERYGIUM WILFORDII Guo Fujiang (Guo FJ); Fang Peifen (Fang Pf) and Li Yuanchao (Li YC) Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . wilforol E C30H48O3 ÏàËÆ¶È:65.6% Phytochemistry 1995 39 1153-1157 Triterpenes from Tripterigium wilfordii Takashi Morota, Chun-Xin Yang, Hiroshi Sasaki, Wan-Zhang Qin, Kô Sugama, Kang-Li Miao, Takaaki Yoshino, Li-Hong Xu, Masao Maruno, Bing-Hui Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . ilexolic acid B ÏàËÆ¶È:65.6% Phytochemistry 1994 37 1517-1575 13C NMR Spectra of pentacyclic triterpenoids¡ªa compilation and some salient features Shashi B. Mahato, Asish P. Kundu Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . compound 379 ÏàËÆ¶È:65.6% Phytochemistry 1994 37 1517-1575 13C NMR Spectra of pentacyclic triterpenoids¡ªa compilation and some salient features Shashi B. Mahato, Asish P. Kundu Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . ilexolic acid B C30H46O6 ÏàËÆ¶È:65.6% Phytochemistry 1993 33 1475-1480 Triterpenes and triterpene glycosides from the leaves of Ilex rotunda Kayoko Amimoto, Kazuko Yoshikawa, Shigenobu Arihara Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . oleanolic acid ÏàËÆ¶È:65.6% Chinese Traditional and Herbal Drugs 2002 33 679-680 Studies on chemical constituents in root back of Paeonia suffruticosa WU Shao hua; MA Yun bao; LUO Xiao dong; HAO Xiao jiang; WU Da gang Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . Simiarenol C30H50O ÏàËÆ¶È:65.6% Archives of Pharmacal Research 2001 24 312-315 Phytochemical constituents of Artemisia stolonifera Hak Cheol Kwon, Sang Un Choi and Kang Ro Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . simiarenol ÏàËÆ¶È:65.6% Journal of Shenyang Pharmaceutical University 2009 26 353-356 Isolation and identification of liposoluble components from the root of phragmites communis Trin. LUO Fang, LI Na, CAO G ui-dong, YU Lu, SONG Shao-jiang Structure 13C NMR ̼Æ×Ä£Äâͼ |
4Â¥2013-02-27 21:10:56
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»¯ºÏÎï1 ²éѯ½á¹û£º¹²²éµ½843¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . T-Muurolol C15H26O ÏàËÆ¶È:100% Journal of Natural Products 2009 72 99-101 T-Muurolol Sesquiterpenes from the Marine Streptomyces sp. M491 and Revision of the Configuration of Previously Reported Amorphanes Ling Ding, Roland Pfoh, Stephan Ruhl, Song Qin,and Hartmut Laatsch Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . emt-T-muurolol C15H26O ÏàËÆ¶È:100% Phytochemistry 1994 37 1323-1325 Cadinane-type sesquiterpenoids from the liverwort Scapania undulata Fumihiro Nagashima, Keiko Suda, Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (-)-T-muurolol C15H26O ÏàËÆ¶È:100% Phytochemistry 1992 31 1659-1661 Sesquiterpenes from the roots of Homalomena aromatica T.V. Sung, L. Kutschabsky, A. Porzel, W. Steglich, G. Adam Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . T-muurolol ÏàËÆ¶È:100% Journal of the Chinese Chemical Society 2000 47 555-560 The Chemical Constituents from the Heartwood of Eucalyptus citriodora Ching-Kuo Lee* and Ming-Huey Chang Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . T-muurolol C15H26O ÏàËÆ¶È:100% Journal of Agricultural and Food Chemistry 2012 60 124-128 Phytochemicals from Cunninghamia konishii Hayata Act as Antifungal Agents Sen-Sung Cheng, Min-Jay Chung, Chun-Ya Lin, Ya-Nan Wang, and Shang-Tzen Chang Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . T-Muurolol ÏàËÆ¶È:100% Australian Journal of Chemistry 1986 39 1717-1722 Studies of Australian Soft Corals. XXXIX. New Sesquiterpene Metabolites From Several Xenia Species (Xeniidae, Octocorallia, Anthozoa) BF Bowden, JC Coll and RH Willis Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . ent-T-muurolol ÏàËÆ¶È:100% China Journal of Chinese Materia Medica 2012 37 3426-3429 Sesquiterpenes from stem of Schisandra glaucescens ZHANG Pei-pei; GAO Sha-sha; ZHANG Tian-tian; CHEN Jia-chun; DUAN Hong-quan; FANG Jin-bo Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . torreyol ÏàËÆ¶È:86.6% Phytochemistry 1988 27 1121-1123 Sesquiterpenoids from Pilgerodendron uv¨ªfera M.Luisa Oyarz¨²n,Juan A. Garbarino Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . torreyol ÏàËÆ¶È:86.6% China Journal of Chinese Materia Medica 2012 37 3426-3429 Sesquiterpenes from stem of Schisandra glaucescens ZHANG Pei-pei; GAO Sha-sha; ZHANG Tian-tian; CHEN Jia-chun; DUAN Hong-quan; FANG Jin-bo Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . axinisothiocyanate K C16H25NS ÏàËÆ¶È:81.2% Journal of Natural Products 2008 71(4) 608-614 Isothiocyanate Sesquiterpenes from a Sponge of the Genus Axinyssa Eva Zub¨ªa, Mar¨ªa J. Ortega, Claudia J. Hern¨¢ndez-Guerrero, and J. Luis Carballo Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 15-Hydroxy-Tmuurolol C15H26O2 ÏàËÆ¶È:73.3% Journal of Natural Products 2009 72 99-101 T-Muurolol Sesquiterpenes from the Marine Streptomyces sp. M491 and Revision of the Configuration of Previously Reported Amorphanes Ling Ding, Roland Pfoh, Stephan Ruhl, Song Qin,and Hartmut Laatsch Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . [6-(1-bromo-2-methyl-propyl)-4-dimethyl-1-methylene-4,5,6,7-tetrahydro-1H-indene] C15H21Br ÏàËÆ¶È:73.3% Chemistry-A European Journal 2003 9 5770-5777 Calenzanane Sesquiterpenes from the Red Seaweed Laurencia microcladia from the Bay of Calenzana, Elba Island: Acid-Catalyzed Stereospecific Conversion of Calenzanol into Indene- and Guaiazulene-Type Sesquiterpenes Graziano Guella, Danielle Skropeta, Ines Mancini and Francesco Pietra Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . (2R)-¦Ä-cadin-4-ene-2,10-diol C15H26O2 ÏàËÆ¶È:66.6% Helvetica Chimica Acta 2006 Vol. 89 16 Uncommon Sesquiterpenoids and New Triterpenoids from Jatropha neopauciflora (Euphorbiaceae) Abraham Garc¨ªa and Guillermo Delgado Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . (2R)-¦Ä-cadin-4-ene-2,10-diol C15H26O2 ÏàËÆ¶È:66.6% Helvetica Chimica Acta 2006 Vol. 89 16 Uncommon Sesquiterpenoids and New Triterpenoids from Jatropha neopauciflora (Euphorbiaceae) Abraham Garc¨ªa and Guillermo Delgado Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 6-epi-cubenol ÏàËÆ¶È:66.6% Phytochemistry 2002 59 805-810 epi-Cubebanes from Solidago canadensis Adeleke A. Kasali, Olusegun Ekundayo, Claudia Paul, Wilfried A. König Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . (-)-torreyol ÏàËÆ¶È:66.6% China Journal of Chinese Materia Medica 2006 31 125-128 Studies on chemical constituents of the brown alga Dictyopteris divaricata SONG Fuhang, FAN Xiao, XU Xiuli, WANG Sujuan, LI Shuai, YANG Yongchun, SHI Jiangong Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (+)-10¦Â(H)-muurola-3,7(11)-dien-1-ol C15H24O ÏàËÆ¶È:66.6% Phytochemistry 1999 52 695-704 Sesquiterpene constituents of the liverwort Calypogeia fissa Ute Warmers, Wilfried A. König Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . (¡À) axial-cadinol axial ÏàËÆ¶È:66.6% Phytochemistry 1996 42 1097-1103 Three new oxygenated cadinanes from Baccharis species Carmen L. Queiroga, Vera L. Ferracini, A. J. Marsaioli Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . ( 1R*,4R*,5Z,9S*)-5-isopropyl-3,3,9-trimethylbicyclo[4. 3.0]nona-5-en-4-ol C15H26O ÏàËÆ¶È:66.6% Journal of Natural Products 1991 Vol 54 1025 New Sesquiterpenes and C15 Acetogenins from the Marine Red Alga Laurencia implicata Anthony D. Wright, Gabriele M. König, Otto Sticher Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 1,6-cis-lippifolian-1¦Á-ol-5-one C15H24O2 ÏàËÆ¶È:66.6% Journal of Natural Products 1994 Vol 57 206 Minor Constituents of Lippia integrifolia Cesar A. N. Catal¨¢n, Marina E. P. de Lampasona, In¨¦s J. S. de Fenik, Carlos M. Cerda-Garc¨ªa-Rojas, Yolanda Mora-P¨¦rez, Pedro Joseph-Nathan Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . arenaran A C15H26O ÏàËÆ¶È:66.6% Journal of Natural Products 1995 Vol 58 44-50 The Arenarans, Sesquiterpene Ethers from the Marine Sponge Dysidea arenaria Paul A. Horton, Phillip Crews Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . (+)-T-Cadinol ÏàËÆ¶È:66.6% Phytochemistry 1993 34 441-444 Mono and sesquiterpenoids from Satureja gilliesii Cecilia Labbe, Mariano Castillo, Joseph D. Connolly Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . 8,10-Dihydroselricardine A C15H28O2 ÏàËÆ¶È:66.6% Phytochemistry 1991 30 131-136 Seiricardine A, A phytotoxic sesquiterpene from three Seiridium species pathogenic for cypress Alessandro Ballio, Maria A. Castiglione Morelli, Antonio Evidente, Antonio Graniti, Giacomino Randazzo, Lorenzo Sparapano Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . ¦Ä-cadinene ÏàËÆ¶È:66.6% Phytochemistry 1991 30 1551-1554 Oxygenated sesquiterpenes from the wood of Juniperus oxycedrus A.F. Barrero, J.F. S¨¢nchez, J.E. Oltra, J. Altarejos, N. Ferrol, A. Barrag¨¢n Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . gleenol ÏàËÆ¶È:66.6% Phytochemistry 1991 30 1551-1554 Oxygenated sesquiterpenes from the wood of Juniperus oxycedrus A.F. Barrero, J.F. S¨¢nchez, J.E. Oltra, J. Altarejos, N. Ferrol, A. Barrag¨¢n Structure 13C NMR ̼Æ×Ä£Äâͼ |
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jiangchunyong: ½ð±Ò+1, лл 2013-02-28 09:05:27
jiangchunyong: ½ð±Ò+1, лл 2013-02-28 09:05:27
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²éѯ½á¹û£º¹²²éµ½67¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Compound 2 ÏàËÆ¶È:60% Magnetic Resonance in Chemistry 2000 38 891-893 13C NMR chemical shift assignments for substituted 2-azabicyclo[3.3.1]nonan-3-ones Josefina Quirante, Carmen Escolano, Faïza Diaba, Merc¨¨ Torra and Josep Bonjoch Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 5-acetylhexahydro-4,7-methanobenzotrithiole ÏàËÆ¶È:60% Tetrahedron Letters 2005 46 7077-7079 Conversion of norbornene derivatives into vicinal-dithioethers via S8 activation Sophie Poulain, Sandy Julien, Elisabet Duñach Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . compound compound ÏàËÆ¶È:60% Tetrahedron 1987 43 935-945 Sedum alkaloids. X. Structure and synthesis of new 3- and 5-hydroxypiperidine alkaloids W. Ibebeke-Bomangwa, C. Hootel¨¦(rk) Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (¡À)3-endo-hydroxycineole ÏàËÆ¶È:60% Agricultural and Biological Chemistry 1982 46 2601-2604 Eucalyptus as Biomass. Novel Compounds from Microbial Conversion of 1, 8-Cineole Hiroyuki NISHIMURA, Yoshiaki NOMA, Junya MIZUTANI Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 5a C10H19O2P ÏàËÆ¶È:60% European Journal of Organic Chemistry 2010 363-369 Reactions of the Bornyl and Fenchyl Grignard Reagent with Chlorophosphanes ¨C Diastereoselectivity and Mechanistic Implications Jens Beckmann and Alexandra Sch¨¹trumpf Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 9-hydroxycineole ÏàËÆ¶È:60% Australian Journal of Chemistry 1994 47 1509-1521 2,9-Dihydroxy- and 2,10-Dihydroxy-1,8-cineole. Two New Possum Urinary Metabolites RM Carman, AC Garner and KD Klika Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 6 ÏàËÆ¶È:60% Australian Journal of Chemistry 1994 47 1509-1521 2,9-Dihydroxy- and 2,10-Dihydroxy-1,8-cineole. Two New Possum Urinary Metabolites RM Carman, AC Garner and KD Klika Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Compound 4 ÏàËÆ¶È:54.5% Magnetic Resonance in Chemistry 2000 38 891-893 13C NMR chemical shift assignments for substituted 2-azabicyclo[3.3.1]nonan-3-ones Josefina Quirante, Carmen Escolano, Faïza Diaba, Merc¨¨ Torra and Josep Bonjoch Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 3,11-Dihydroxydodecanoic acid C12H24O4 ÏàËÆ¶È:54.5% Journal of Agricultural and Food Chemistry 2005 53 8987-8992 Chemistry and Bioactivity of Royal Jelly from Greece Eleni Melliou and Ioanna Chinou Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . aldingenin B C15H23O4Br ÏàËÆ¶È:53.3% Phytochemistry 2006 67 1331-1335 Aldingenin derivatives from the red alga Laurencia aldingensis Luciana R. de Carvalho, Mutue T. Fujii, Nidia F. Roque, João Henrique G. Lago Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . canusesnol G C15H26O3 ÏàËÆ¶È:53.3% Journal of Natural Products 2004 67 1893-1896 New Sesquiterpenes from Capsicum annuum Yousuke Kawaguchi, Toshimasa Ochi, Yoshihisa Takaishi, Kazuyoshi Kawazoe, and Kuo-Hsiung Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . rostratin A C18H24N2O6S2 ÏàËÆ¶È:50% Journal of Natural Products 2004 67 1374-1382 Isolation and Structure Assignments of Rostratins A−D, Cytotoxic Disulfides Produced by the Marine-Derived Fungus Exserohilum rostratum Ren Xiang Tan, Paul R. Jensen, Philip G. Williams, and William Fenical Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 5a ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1996 44 337-342 Five New Monoterpene Glycosides and Other Compounds form Foeniculi Fructus (Fruit of Foeniculum vulgare MILLER) Masateru ONO,Yasuyuki ITO,Thoru ISHIKAWA,Junichi KITAJIMA,Yasuko TANAKA,Yujiro NIIHO and Toshihiro NOHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 7 C10H20O2 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1981 29 1636-1643 The Constituents of Schizonepeta tenuifolia BRIQ. I. Structures of Two New Monoterpene Glucosides, Schizonepetosides A and B HIROSHI SASAKI,HEIHACHIRO TAGUCHI,TOHRU ENDO,ITIRO YOSIOKA and YOICHI IITAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 4-p-menthane-1,8,9-triol ÏàËÆ¶È:50% Acta Pharmaceutica Sinica 1992 27 752-757 NEW MONOTERPENOIDS FROM CYNANCHUM HANCOCKIANUM HX Lou; X Li; TR Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . (1S,2R,4S,5R)-2,5-dihydroxy-1,8-cineole C10H18O3 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1998 46 1738-1742 Water-Soluble Constituents of Fennel. VI. 1, 8-Cineole Type Glycosides Toru ISHIKAWA,Junichi KITAJIMA,Yasuko TANAKA,Masateru ONO,Yasuyuki ITO and Toshihiro NOHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (1S,2S,4S,5R)-2,5-dihydroxy-1,8-cineole C10H18O3 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1998 46 1738-1742 Water-Soluble Constituents of Fennel. VI. 1, 8-Cineole Type Glycosides Toru ISHIKAWA,Junichi KITAJIMA,Yasuko TANAKA,Masateru ONO,Yasuyuki ITO and Toshihiro NOHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . kirilowin F C15H21N3O15 ÏàËÆ¶È:50% Fitoterapia 2008 79 451-455 Six new glucose esters of 3-nitropropanoic acid from Indigofera kirilowii Yanfang Su , Min L¨¹ a, Fengying Yang , Chunzheng Li , Lizhi Di , Di Wua, Zengjun Guo , Juxian L¨¹ , Dean Guo Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 4,10-diacetate of 4-oxo-cis-myrtanol ÏàËÆ¶È:50% Phytochemistry 1997 45 935-943 Biotransformation of (− -cis-myrtanol and (+)-trans-myrtanol by plant pathogenic fungus, Glomerella cingulataMitsuo Miyazawa, Yasuhiro Suzuki, Hiromu Kameoka Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 1,8dihydroxy-neomenthol ÏàËÆ¶È:50% Phytochemistry 1994 35 1465-1467 Biotransformation of (− - and (+)-neomenthols and isomenthol by Aspergillus nigerHironobu Takahashi, Yoshiaki Noma, Masao Toyota, Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 2-Methyl-2-(2-oxo-1,3,2-dioxaphosphinan-2-yl)-3,4-dihydro-2H-pyrrole 1-oxide [CyDEPMPO] C8H14NO4P ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2011 19 2218-2230 CyDEPMPOs: A class of stable cyclic DEPMPO derivatives with improved properties as mechanistic markers of stereoselective hydroxyl radical adduct formation in biological systems Gaëlle Gosset, Jean-Louis Cl¨¦ment, Marcel Culcasi, Antal Rockenbauer, Sylvia Pietri Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 4¦Á-hydroxy-iso-menthol C10H20O2 ÏàËÆ¶È:50% Phytochemistry 1988 27 3861-3869 Preparation of biologically active substances and animal and microbial metabolites from menthols,cineoles and kauranes Yoshinori Asakawa,Reiko Matsuda,Motoo Tori,Toshihiro Hashimoto Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . 1-hydroxy-neo-menthol ÏàËÆ¶È:50% Phytochemistry 1988 27 3861-3869 Preparation of biologically active substances and animal and microbial metabolites from menthols,cineoles and kauranes Yoshinori Asakawa,Reiko Matsuda,Motoo Tori,Toshihiro Hashimoto Structure 13C NMR ̼Æ×Ä£Äâͼ |
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-cis-myrtanol and (+)-trans-myrtanol by plant pathogenic fungus, Glomerella cingulata