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ÈܼÁ¾ùΪ뮴úÂÈ·Â 1. 17.275,17.791,26.018,27.429,29.767,31.337,33.971,41.279,44.967,112.159,138.599,146.181,170.670,208.736,209.176 2. 15.598,20.341,21.950,23.028,25.297,28.628,29.531,42.068,46.728,49.445,55.743,57.026,73.054,211.430 3. 16.304,17.564,32.840,35.451,59.348,75.520,111.188,123.573,139.449,147.334 4. 18.247,22.625,31.269,33.090,63.196,80.825,84.657,110.634,144.883 |
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²éѯ½á¹û£º¹²²éµ½85¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . 4,5-seco-Guaia-1(10),11-diene-4,5-dioxo C15H22O2 ÏàËÆ¶È:100% Tetrahedron 2011 67 9193-9198 Sesquiterpenoids, alantolactone analogues, and seco-guaiene from the roots of Inula helenium Hai-Long Jiang, Jia Chen, Xiao-Jie Jin, Jun-Li Yang, Ya Li, Xiao-Jun Yao , Quan-Xiang Wu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . mandassidione C15H22O2 ÏàËÆ¶È:100% Phytochemistry 1988 27 3319-3321 Mandassidione and other sesquiterpenic ketones from Cyperus articulatus B. Nyasse,R. Ghogomu,Tih B.L. Sondengam,M. T. Martin,B. Bodo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . cyperusol B1 C15H24O2 ÏàËÆ¶È:80% Journal of Natural Products 2004 67 569-576 Structures of New Sesquiterpenes and Hepatoprotective Constituents from the Egyptian Herbal Medicine Cyperus longus Fengming Xu, Toshio Morikawa, Hisashi Matsuda, Kiyofumi Ninomiya, and Masayuki Yoshikawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . mandassidione ÏàËÆ¶È:80% China Journal of Chinese Materia Medica 2010 35 315-322 Terpenoids of Heteroplexis micocephala and their bioactivities FAN Xiaona; LIN Sheng; ZHU Chenggen; HU Jinfeng; LIU Yang; CHEN Xiaoguang; CHEN Naihong; WANG Wenjie; SHI Jiangong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . cyperusol B2 C15H24O2 ÏàËÆ¶È:73.3% Journal of Natural Products 2004 67 569-576 Structures of New Sesquiterpenes and Hepatoprotective Constituents from the Egyptian Herbal Medicine Cyperus longus Fengming Xu, Toshio Morikawa, Hisashi Matsuda, Kiyofumi Ninomiya, and Masayuki Yoshikawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 10-epi-Acora-3,11-dien-15-ol ÏàËÆ¶È:66.6% Flavour and Fragrance Journal 2000 15 61-83 1,7-Cyclogermacra-1(10),4-dien-15-al, a sesquiterpene with a novel skeleton, and other sesquiterpenes from Haitian vetiver oil Peter Weyerstahl, Helga Marschall, Ute Splittgerber and Dietmar Wolf Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . Huperzine W C14H21NO2 ÏàËÆ¶È:60% Chinese Chemical Letters 2002 13 331-332 Huperzine W, a Novel 14 Carbons Lycopodium Alkaloid from Huperzia serrata Chang Heng TAN, Xiao Qiang MA, Guo Fu CHEN, Shan Hao JIANG,Da Yuan ZHU Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 4 (15)-cadinene-6,10-diol C23H24O11 ÏàËÆ¶È:60% Journal of Asian Natural Products Research 2004 6 199-204 CHEMICAL CONSTITUENTS FROM ALPINIA TONKINENSIS JIAN ZHANG and LING-YI KONG Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . (-)-huperzine W C14H21NO2 ÏàËÆ¶È:60% Natural Products and Bioprospecting 2012 2 255-257 One-step synthesis of Lycopodium alkaloid (-)-huperzine W via Suzuki-Miyaura coupling Tao Xu, Shi-Zhi Jiang, Huai-Rong Luo, Yu-Rong Yang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . (1S,6R,7S,10S)-7-isopropyl-10-methyl-4-methylenedecahydronaphthalene-6,10-diol C15H26O2 ÏàËÆ¶È:60% Acta Crystallographica Section E 2007 63 o3579 6¦Â,10¦Â-Cadinene-6,10-diol: a sesquiterpenoid from the rhizome of Acorus calamus L. Wei-Wei Dong, Kai-Bei Yu, Jian-Min Yue and Run-Hua Lu Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-10-14 09:58:54
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²éѯ½á¹û£º¹²²éµ½453¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . compound E ÏàËÆ¶È:100% Phytochemistry 1989 28 1425-1426 Sesquiterpenes from Eremophila species Kim A. Dastlik,Peter G. Forster,Emilio L. Ghisalberti,Phillip R. Jefferies Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . oplopanone ÏàËÆ¶È:100% Archives of Pharmacal Research 1997 20 363-367 Sesquiterpene components from the flower buds of Magnolia fargesii Keun Young Jung, Dong Seon Kim, Sei Ryang Oh, Im Seon Lee and Jung Joon Lee, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . ent-oplopanone C15H26O2 ÏàËÆ¶È:93.3% Chemical & Pharmaceutical Bulletin 1987 35 124-135 Marine Natural Products. XVII. Nephtheoxydiol, a New Cytotoxic Hydroperoxy-Germacrane Sesquiterpene, and Related Sesquiterpenoids from an Okinawan Soft Coral of Nephthea sp. (Nephtheidae) ISAO KITAGAWA,ZHENG CUI,BYENG WHA SON,MOTOMASA KOBAYASHI and YOSHIMASA KYOGOKU Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . oplopanone C15H26O4 ÏàËÆ¶È:93.3% Natural Product Research 2003 17 445-449 A new xanthone from Hedychium gardnerianum Maria João Carvalho; Lu¨ªs M. Carvalho; Ana Margarida Ferreira; Artur M. S. Silva Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . (-)-oplopanone ÏàËÆ¶È:93.3% China Journal of Chinese Materia Medica 2009 34 990-993 Studies on chemical constituents in fruit of Alpinia oxyphylla XU Junju, TAN Ninghua, ZENG Guangzhi, HAN Hongjin, HUANG Huoqiang, JI Changjiu, ZHU Meiju, ZHANG Yumei Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . oplopanone C15H26O2 ÏàËÆ¶È:93.3% China Journal of Chinese Materia Medica 2003 28 342-344 Studies on the Constituents in Rhizome of Homalomena occuta HU Yongmei, YANG Zhonglin, YE Wencai, CHONG Qihou Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . Oplopanone ÏàËÆ¶È:93.3% Phytochemistry 1995 39 603-607 Sesquiterpenes from leaves of Cryptomeria japonica Wen-Chiung Su, Jim-Min Fang, Yu-Shia Cheng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . Oplopanone ÏàËÆ¶È:93.3% Natural Product Research 2012 26 850-858 A new sesquiterpenoid from the rhizomes of Homalomena sagittifolia K.C. Wong, Abdul Hamid, I.M.S. Eldeen, M. Zaini Asmawi,S. Baharuddin, H.S. Abdillahi and J. Van Staden Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . oplopanone ÏàËÆ¶È:93.3% Phytochemistry 1983 22 1457-1459 Sesquiterpene alcohols and triterpenoids from Liatris microcephala Werner Herz, Kinzo Watanabe Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . oplopanone ÏàËÆ¶È:93.3% Chinese Traditional and Herbal Drugs 2009 40 29-32 ÒæÖÇÈÊ»¯Ñ§³É·ÖÑо¿ Áõéª;ÓÚÐÂÓî;ÕÔºì;ÕÔÓàÇì Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . Oplopanone ÏàËÆ¶È:93.3% Chinese Journal of Natural Medicines 2008 6 339-341 Sesquiterpenes from the Stems of Croton caudatus Geisel. var. tomentosus Hook. WANG Yuan; ZOU Zhong-Mei Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . Oplopanone ÏàËÆ¶È:93.3% Archives of Pharmacal Research 2010 33 1317-1323 Scopoletin from the flower buds of Magnolia fargesii inhibits protein glycation, aldose reductase, and cataractogenesis Ex Vivo Jun Lee, Nan Hee Kim, Joo Won Nam, Yun Mi Lee and Dae Sik Jang, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . oplopanone ÏàËÆ¶È:93.3% Journal of the Chinese Chemical Society 2002 49 427-431 Cytotoxic Components from the Leaves of Schefflera taiwaniana Yueh-Hsiung Kuo*, Jir-Mehng Lo and Yih-Fwu Chan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . oplopanone ÏàËÆ¶È:93.3% Journal of the Chinese Chemical Society 2005 52 369-374 Terpenoids from the Flower of Cacalia tangutica Xia Liu, Quan-Xiang Wu and Yan-Ping Shi* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . subdigitatone C15H26O2 ÏàËÆ¶È:93.3% Indian Journal of Chemistry 1995 34B 664-665 New sesquiterpene from Artemisia subdigitata Yu Li, Yanping Shi & Yang Li Structure 13C NMR ̼Æ×Ä£Äâͼ |
3Â¥2013-10-14 09:59:49
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²éѯ½á¹û£º¹²²éµ½49¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . (6RS)-(E)-3,7-Dimethyl-2,7-octadiene-1,6-diol ÏàËÆ¶È:100% Journal of Agricultural and Food Chemistry 1998 46 1966-1970 (S)-3,7-Dimethyl-5-octene-1,7-diol and Related Oxygenated Monoterpenoids from Petals of Rosa damascena Mill. Holger Knapp, Markus Straubinger, Selenia Fornari, Noriaki Oka, Naoharu Watanabe, and Peter Winterhalter Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . compound 25 ÏàËÆ¶È:90% Organic Magnetic Resonance 1975 7 426-432 13C-NMR-Spektren von Monoterpenen F. Bohlmann, R. Zeisberg and E. Klein Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . (3S)-(E)-2,6-dimethyl-10-methylene-1,6,11-dodecatrien-3-ol ÏàËÆ¶È:60% Journal of Natural Products 1992 Vol 55 428 New Farnesane Sesquiterpenes from Hebeloma senescens Maurizio Bocchi, Luigi Garlaschelli, Giovanni Vidari, Giorgio Mellerio Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . compound 2 C10H14O3 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 2009 57 294-297 Structure of New Monoterpene Glycoside from Sibiraea angustata RCHD. and Its Anti-obestic Effect Yoshiaki Ito, Satoshi Kamo, Samir Kumar Sadhu, Takashi Ohtsuki, Masami Ishibashi and Yoshihiro Kano Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . compound 10f C10H10N4O2 ÏàËÆ¶È:60% Journal of Heterocyclic Chemistry 2000 37 1041-1048 Reactivity studies of ethyl(Z)-N-(2-amino-1,2-dicyanovinyl) formimidate with carbonyl compounds in the presence of base M. Jos¨¦alves, M. Alice Carvalho, M. Fernanda, J. R. P. Proença and Brian L. Booth Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . (2Z)-2,6-dimethylhepta-2,6-diene-1,5-diol ÏàËÆ¶È:60% Russian Journal of Organic Chemistry 2011 47 1287-1292 Synthesis of 6-hydroxycarvone derivatives and their oxidative decyclization with lead tetraacetate R. F. Valeev, R. F. Bikzhanov, N. K. Selezneva, F. A. Gimalova and M. S. Miftakhov Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . (7RS)-(2E)-3,7-Dimethyl-2-octene-1,8-diol ÏàËÆ¶È:60% Journal of Agricultural and Food Chemistry 1998 46 1966-1970 (S)-3,7-Dimethyl-5-octene-1,7-diol and Related Oxygenated Monoterpenoids from Petals of Rosa damascena Mill. Holger Knapp, Markus Straubinger, Selenia Fornari, Noriaki Oka, Naoharu Watanabe, and Peter Winterhalter Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . (7RS)-(2Z)-3,7-Dimethyl-2-octene-1,8-diol ÏàËÆ¶È:60% Journal of Agricultural and Food Chemistry 1998 46 1966-1970 (S)-3,7-Dimethyl-5-octene-1,7-diol and Related Oxygenated Monoterpenoids from Petals of Rosa damascena Mill. Holger Knapp, Markus Straubinger, Selenia Fornari, Noriaki Oka, Naoharu Watanabe, and Peter Winterhalter Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 5-(3-Furyl)-2-methyl-1-pentene-3-ol ÏàËÆ¶È:60% European Journal of Organic Chemistry 1992 1992 279-281 Terpenes and Terpene Derivatives, XXVIII. New Monoterpene Derivatives from the Essential Oil of Artemisia salsoloides Peter Weyerstahl, Hans-Christian Wahlburg, Vijay K. Kaul and Stanislaw Lochynski Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . Tolbutamide ÏàËÆ¶È:60% Applied Microbiology and Biotechnology 2006 72 486-491 Biotransformation of tolbutamide to 4¡ä-hydroxytolbutamide by the fungus Cunninghamella blakesleeana Haihua Huang, Xiuwei Yang, Qiang Li, Lu Sun, Dafang Zhong Structure 13C NMR ̼Æ×Ä£Äâͼ |
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²éѯ½á¹û£º¹²²éµ½25¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . 5,6-epoxy-5-isopropyl-6-methyl-hepy-3-in-2-on C11H16O2 ÏàËÆ¶È:60% Helvetica Chimica Acta 1977 60 743-767 Photochemische Reaktionen. 93. Mitteilung. Zur Photochemie konjugierter Epoxy-inone: Die UV.-Bestrahlung von 5,6-Epoxy-5-isopropyl-6-methyl-hept-3-in-2-on Herbert Eichenberger, Hans Richard Wolf and Oskar Jeger Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . (Z)-6-hydroxymethyl-2-methylocta-1,6-diene-3,8-diol C10H18O3 ÏàËÆ¶È:60% Australian Journal of Chemistry 1989 42 1983-1993 Tropical Marine-Algae. VI. New Monoterpenes From Several Collections of Chondrococcus hornemannii (Rhodophyta, Gigartinales, Rizophyllidaceae) JC Coll and AD Wright Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . compound 8a ÏàËÆ¶È:55.5% Zeitschrift f¨¹r Naturforschung B 2007 62 1174-1182 Triethylborane: An "Old" Reagent with New Functions. 1,2-Hydroboration B. Wrackmeyer, E. Khan, S. Bayer, and K. Shahid Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . compound C8H14O ÏàËÆ¶È:55.5% Journal of the American Chemical Society 2004 126 14720-14721 Total Synthesis of Kendomycin: A Macro−C−Glycosidation Approach Yu Yuan, Hongbin Men, and Chulbom Lee Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . compound 21' C9H18O3 ÏàËÆ¶È:55.5% Tetrahedron 2012 68 8994-9003 Enantiodivergent synthesis of (+)- and (− -isolaurepanGonzalo Pazos, Manuel P¨¦rez, Zoila G¨¢ndara, Generosa G¨®mez, Yagamare Fall Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 4-nonyn-1-ol ÏàËÆ¶È:55.5% Journal of Chemical Ecology 2010 36 923-932 Identification of the Sex Pheromone of a Protected Species, the Spanish Moon Moth Graellsia isabellae Jocelyn G. Millar, J. Steven McElfresh, Carmen Romero, Marta Vila, Neus Mar¨ª-Mena, Carlos Lopez-Vaamonde Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 4-Isopropyl-2,7-dimethyl-3-oxa-1.4.7-octatrien C12H20O ÏàËÆ¶È:54.5% Helvetica Chimica Acta 1981 64 198-214 Photochemische Reaktionen. 117. Mitteilung [1] Zur Photochemie von 5,6-Epoxydienen und konjugierten 5,6-Epoxytrienen Alex Peter Alder, Hans Richard Wolf, Oskar Jeger Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 7-dodecyn-1-ol ÏàËÆ¶È:54.5% Journal of Chemical Ecology 2006 32 1085-1099 Isolation, Identification, Synthesis, and Field Evaluation of the Sex Pheromone of the Brazilian Population of Spodoptera frugiperda Luciane G. Batista-Pereira, Kathrin Stein, Andr¨¦ F. de Paula, Jardel A. Moreira, Ivan Cruz, Maria de Lourdes C. Figueiredo, Jos¨¦ Perri Jr., Arlene G. Corr¨ºa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . masutakic acid A C10H16O4 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 2001 49(3) 327-329 A Benzofuran Glycoside and an Acetylenic Acid from the Fungus Laetiporus sulphureus var. miniatus Kazuko YOSHIKAWA, Shinya BANDO,Shigenobu ARIHARA,Eiko MATSUMURA,and Satoshi KATAYAMA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . (2R,3R,4R)-5-Chrysanthemen-1,4-diol C10H18O2 ÏàËÆ¶È:50% Journal of Natural Products 2004 67 37-41 Polyoxygenated Eudesmanes and trans-Chrysanthemanes from the Aerial Parts of Santolina insularis Ernesto Fattorusso, Federico U. Santelia, Giovanni Appendino, Mauro Ballero, and Orazio Taglialatela-Scafati Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . jatamanin F C10H16O4 ÏàËÆ¶È:50% Journal of Natural Products 2010 73 632-638 Iridoids and Lignans from Valeriana jatamansi Sheng Lin, Tao Chen, Xiao-Hua Liu, Yun-Heng Shen, Hui-Liang Li, Lei Shan, Run-Hui Liu, Xi-Ke Xu, Wei-Dong Zhang and Hui Wang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 2-butyl-5-ethynyltetrahydrofuran(Minor isomer) C10H16O ÏàËÆ¶È:50% Organic Letters 2007 Vol. 9, No. 10 1975-1978 Ene-yne Tetrahydrofurans from the Sponge Xestospongia muta. Exploiting a Weak CD Effect for Assignment of Configuration Brandon I. Morinaka, Colin K. Skepper, and Tadeusz F. Molinski Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 2Z,4E-decadienoic methyl ester ÏàËÆ¶È:50% Phytochemistry 1988 27 207-212 Diterpenes from the latex of Euphorbia broteri Julio Gonz¨¤lez Urones,Pilar Basabe Barcala,Ma Jos¨¨ Sexmero Cuadrado,Isidro S¨¤nchez Marcos Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 2,2,8,8-tetrahexyl-3,6,9-trioxaundecane-1,11-diol ÏàËÆ¶È:50% Journal of Heterocyclic Chemistry 2001 38 1259-1264 Synthesis of new proton-ionizable crown ether compounds containing substituted lh-pyridin-4-one subcyclic units Peter Huszthy, Julia Kertesz, Jerald S. Bradshaw, Reed M. Izatt and J. Ty Redd Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . (S)-1-((3R,5R,S)-5-Methyl-5-(2-((triisopropylsilyl) oxy)ethyl)-1,2-dioxolan-3-yl)ethane-1,2-diol C17H36O5Si ÏàËÆ¶È:50% Tetrahedron 2012 68 3717-3724 Exploratory studies toward the synthesis of the peroxylactone unit of plakortolides Bogdan Barnych, Jean-Michel Vat¨¨le Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . 1-(2'-(1''-hydroxy-1''-methylethyl)thien-3'-ylmethyl)-3,3,4,4-tetramethylsuccinimide C16H23NO3S ÏàËÆ¶È:50% Heterocycles 2001 54 275-282 Azepine and [1,3]Oxazepine Fused Ring Construction through a Cationic Cyclization: an N-acyliminium Ion Trapping of an Oxygen Atom or Olefin Aïcha Mamouni, Adam Daïch, Stefan Marchalin, and Bernard Decroix Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . 2-(2-methoxyethoxy)-5-methyl-5-hexen-2-yl hydroperoxide ÏàËÆ¶È:50% Heterocycles 2000 53 1293-1304 Synthesis of 3-Hydroperoxy (or Hydroxy)-substituted 1,2-Dioxanes and 1,2-Dioxepanes by the Ozonolysis of Unsaturated Hydroperoxy Acetals Takahiro Tokuyasu, Toyonari Ito, Araki Masuyama, and Masatomo Nojima* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . 5-isopropenyl-2-methyltetrahydrofuran-2-acetaldehyde C10H16O2 ÏàËÆ¶È:50% Russian Journal of Organic Chemistry 2002 38 1594-1605 Transformations of 6,7-Epoxy Derivatives of Citral and Citronellal in Various Acidic Media O. I. Yarovaya, O. V. Salomatina, D. V. Korchagina, M. P. Polovinka and V. A. Barkhash Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . N,5-bis(tert-butyldimethylsilyloxy)pentanamide C17H39NO3Si2 ÏàËÆ¶È:50% European Journal of Organic Chemistry 2011 2293-2300 Glucosinolate Synthesis: a Hydroxamic Acid Approach Deimante Cerniauskaite, Jolanta Rousseau, Algirdas Sackus, Patrick Rollin and Arnaud Tatibouët Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . 9-tetradecyn-1-ol ÏàËÆ¶È:50% Journal of Chemical Ecology 2006 32 1085-1099 Isolation, Identification, Synthesis, and Field Evaluation of the Sex Pheromone of the Brazilian Population of Spodoptera frugiperda Luciane G. Batista-Pereira, Kathrin Stein, Andr¨¦ F. de Paula, Jardel A. Moreira, Ivan Cruz, Maria de Lourdes C. Figueiredo, Jos¨¦ Perri Jr., Arlene G. Corr¨ºa Structure 13C NMR ̼Æ×Ä£Äâͼ |
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