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111 1 . umbelliferone C9H6O3 ÏàËÆ¶È:100% Acta Botanica Yunnanica 2000 22(2) 166-168 The Chemical Constituents from Roots of Ipomoea digitata DAI Hao-Fu,XIONGJiang,ZHOU Jun,DING Zhong-Tao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 1 C9H6O3 ÏàËÆ¶È:100% Natural Product Research 2008 22 365-370 Separation and identification of botanical insecticide 7-hydroxycoumarin and its biological activity against Aphis craccivora and Culex pipiens pallens Tang Xiaorong; Hou Taiping Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . Umbelliferone ÏàËÆ¶È:100% Korean Journal of Pharmacognosy 2007 38(4) 387-393 Isolation of Melanin Biosynthesis Inhibitory Compounds from the Phellodendri Cortex Lee, Jong-Gu; Choi, Ji-Young; Oh, Joon-Seok; Jung, Hee-Wook; Choi, Eun-Hyang; Lee, Hee-Sang; Kim, Jeong-Ah; Chang, Tae-Soo; Son, Jong-Keun; Lee, Seung-Ho Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . umbelliferone ÏàËÆ¶È:100% Food Chemistry 2010 120 825-830 Umbelliferone ¨C An antioxidant isolated from Acacia nilotica (L.) Willd. Ex. Del. Rajbir Singh, Bikram Singh, Sukhpreet Singh, Neeraj Kumar, Subodh Kumar, Saroj Arora Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . umbelliferone ÏàËÆ¶È:100% European Journal of Medicinal Chemistry 2009 44 2252-2259 Antiamoebic coumarins from the root bark of Adina cordifolia and their new thiosemicarbazone derivatives Prince Firdoos Iqbal, Abdul Roouf Bhat, Amir Azam Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . umbelliferone ÏàËÆ¶È:100% Chinese Traditional and Herbal Drugs 2014 45 333-336 Chemical constituents from stems of Ficus tsiangii WANG Yan-liang, DUAN Song-leng, ZHANG Qing-ying, CHENG Wei, LIANG Hong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 7-Hydroxycoumarin C9H6O3 ÏàËÆ¶È:100% Chemistry of Natural Compounds 2011 46 959-960 Chemical constituents of the aerial part of Atractylodes macrocephala Wei Peng, Ting Han, Yang Wang, Wen-Bo Xin and Cheng-Jian Zheng, et al. Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . Umbelliferone ÏàËÆ¶È:100% Journal of Chinese Pharmaceutical Sciences 2012 21 428-434 Chemical constituents of Pseudolarix kaempferi Gord Tianzhi Cai; Wen Qi; Lianmei Yang; Guangzhong Tu; Rong Yang; Kehui Xie; Hongzheng Fu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 7-hydroxycoumarin C9H6O3 ÏàËÆ¶È:100% Central South Pharmacy 2011 9 92-95 Chemical constituents from Morus alba L. YANG Yong-yu, ZENG Guang-yao, TAN Jian-bing, LI Xin, FENG Xu-qiang, WANG Ya-jing, ZHOU Ying-jun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . umbelliferone C9H6O3 ÏàËÆ¶È:100% Chemistry of Natural Compounds 1998 34 517-548 Coumarins: Plants, structures, properties Chapter II. Physical Constants and Spectral Characteristics of Coumarins (continued) CNC Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 222 1 . 3¦Â-hydroxysandaracopimaric acid C20H30O3 ÏàËÆ¶È:75% Journal of Asian Natural Products Research 2002 4 147-154 NON-TAXANE COMPOUNDS FROM THE BARK OF TAXUS YUNNANENSIS SHENG-HONG LI, HONG-JIE ZHANG, PING YAO, XUE-MEI NIU,WEI XIANG and HAN-DONG SUN Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . (1R,2R,6S)-3-Benzyloxycarbonyl-2-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]-7-oxa-3-azabicyclo[4.1.0]heptane C18H23NO5 ÏàËÆ¶È:62.5% Organic & Biomolecular Chemistry 2012 10 9278-9286 Stereoselective synthesis and biological evaluation of D-fagomine, D-3-epi-fagomine and D-3,4-epi-fagomine analogs from D-glyceraldehyde acetonide as a common building block J. Alberto D¨ªez, Jos¨¦ A. G¨¢lvez, Mar¨ªa D. D¨ªaz-de-Villegas, Ram¨®n Badorrey, Barbara Bartholomew and Robert J. Nash Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . compound 33 ÏàËÆ¶È:60% Natural Product Communications 2008 3 399-412 Structural Elucidation of Pimarane and IsopimaraneDiterpenoids: The 13C NMR Contribution Ana M. L. Seca, Diana C. G. A. Pinto and Artur M. S. Silva Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . (S)-(E)-{5-(2,2-dimethyl-6-methylenecyclohexyl)-3-methylpent-2-enyl}-phenylsulfide ÏàËÆ¶È:57.8% Natural Product Communications 2014 9 329-335 Use of (S)-trans-¦Ã-Monocyclofarnesol as a Useful Chiral Building Block for the Stereoselective Synthesis of Diterpenic Natural Products Stefano Serra, Alessandra A. Cominetti and Veronica Lissoni Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . compound 1c ÏàËÆ¶È:57.1% Journal of Natural Products 1983 Vol 46 262-273 Plantes De Nouvelle-Caledonie. LXXVII. Diterp¨¨nes D'Agathis lanceolata Duc Do Khac Manh, Josette Bastard, Marcel F¨¦tizon, Thierry S¨¦venet Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . dehydro-¦Â-monocyclonerolidol C15H24 ÏàËÆ¶È:56.2% Phytochemistry 1996 43 1285-1291 Africane- and monocyclofarnesane-type sesquiterpenoids from the liverwort Porella subobtusa Fumihiro Nagashima, Hiromi Izumo, Atsushi Ishimaru, Shiori Momasaki, Masao Toyota, Toshihiro Hashimoto, Yoshinori Asakawa Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . N-cyclohexyl-a-methyl-2-(2-fluoro-5-nitrophenyl)ethanamine C15H21FN2O2 ÏàËÆ¶È:56.2% Journal of Heterocyclic Chemistry 2009 46 629-634 (¡À)-1,2-Dialkyl-5-nitro-2,3-dihydro-1H-indoles by a tandem reductive amination-SNAr reaction Richard A. Bunce,Takahiro Nago and Brian White Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 9 C14H22O ÏàËÆ¶È:56.2% Tetrahedron Letters 2003 44 6463-6464 First enantioselective synthesis and determination of the absolute configuration of natural (+)-dehydro-¦Â-monocyclonerolidol Elie Palombo, G¨¦rard Audran, Honor¨¦ Monti Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . dehydro-¦Â-monocyclonerolidol C15H24 ÏàËÆ¶È:56.2% Tetrahedron Letters 2003 44 6463-6464 First enantioselective synthesis and determination of the absolute configuration of natural (+)-dehydro-¦Â-monocyclonerolidol Elie Palombo, G¨¦rard Audran, Honor¨¦ Monti Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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