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13C NMR (100 MHz, CDCl3) ¦Ä14.1,19.7,22.7,24.5,27.1,28.0,29.4,29.7,30.0,30.2,31.4,31.9,32.8,34.5,34.9,37.1,37.4,37.5,39.4,119.1,124.0,124.5,138.6,147.1 [ Last edited by À±±ÊvСРon 2014-5-16 at 06:29 ] |
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²éѯ½á¹û£º¹²²éµ½2118¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 9-acetyl-2,6,12,16-tetramethylheptadecanal C23H44O2 ÏàËÆ¶È:66.6% Australian Journal of Chemistry 1993 46 907-915 The Structure of a New C25 Isoprenoid Alkene Biomarker From Diatomaceous Microbial Communities RE Summons, RA Barrow, RJ Capon, JM Hope and C Stranger Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 12b ÏàËÆ¶È:66.6% Canadian Journal of Chemistry 1991 69 1100-1106 Stereoselective syntheses of isomers of 3,7-dimethylnonadecane, a sex pheromone of the alfalfa blotch leafminer (Agromyza frontella (Rondani)) David Miller, François Bilodeau, Robert H. Burnell Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 1-benzoxy-(4S,8S,12S,16S,20S)-4,8,12,16,20-pentamethyl-heptacosane C39H72O ÏàËÆ¶È:66.6% The Journal of Organic Chemistry 2013 78 5970-5986 Highly Stereocontrolled Total Synthesis of ¦Â-d-Mannosyl Phosphomycoketide: A Natural Product from Mycobacterium tuberculosis Nan-Sheng Li, Louise Scharf, Erin J. Adams, and Joseph A. Piccirilli Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 24¦Î,25-dimethyl-3¦Á-hydroxyl-cholest-5-ene-2¦Â-ol sodium sulfate C29H49O5SNa ÏàËÆ¶È:65.5% Natural Product Research 2007 21 953-958 A new cytotoxic cholesterol sulfate from marine sponge Halichondria rugosa Hong-Jun Zhang; Jing-Bo Sun; Hou-Wen Lin; Zeng-Lei Wang; Hua Tang; Ping Cheng; Wan-Sheng Chen; Yang-Hua Yi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 29,30-nordimethyl lanost-2-en ÏàËÆ¶È:64.2% Indian Journal of Chemistry Section B 2007 46B 173-176 Two new terpenes from the lichen Parmelia perlata Abdullah,S Tarique; Hamid,Hinna; Ali,Mohammad; Ansari,S H; Alam,M Sarwar Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . (2R/S,3S,7S,15S)-3,7,15-trimethyl-2-heptacosanol C30H62O ÏàËÆ¶È:64% European Journal of Organic Chemistry 2000 2000 1307-1312 Synthesis of (3S,7S)- and (3S,7S,15S)- Stereoisomers of 3,7-Dimethyl-2-heptacosanone and 3,7,15-Trimethyl-2-heptacosanone, the Ketones Identified from the Locust Schistocerca gregaria Yoshihide Nakamura and Kenji Mori Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . (3S,7S,15S)-3,7,15-trimethyl-2-heptacosanone C30H60O ÏàËÆ¶È:64% European Journal of Organic Chemistry 2000 2000 1307-1312 Synthesis of (3S,7S)- and (3S,7S,15S)- Stereoisomers of 3,7-Dimethyl-2-heptacosanone and 3,7,15-Trimethyl-2-heptacosanone, the Ketones Identified from the Locust Schistocerca gregaria Yoshihide Nakamura and Kenji Mori Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . strongylodiol G C24H42O2 ÏàËÆ¶È:62.5% Journal of Natural Products 2005 68 1001-1005 Acetylenic Strongylodiols from a Petrosia (Strongylophora) Okinawan Marine Sponge Kinzo Watanabe, Yuichiro Tsuda, Maki Hamada, Miki Omori, Go Mori,Kazuo Iguchi, Hideo Naoki, Tsuyoshi Fujita, and Rob W. M. Van Soest Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . (5S)-hydroxy-16-methyleicos-(3Z)-en-1-yne C21H38O ÏàËÆ¶È:62.5% Journal of Natural Products 1995 Vol 58 1801-1807 Antitumor Activity and Stereochemistry of Acetylenic Alcohols from the Sponge Cribrochalina vasculum Yali F. Hallock, John H. Cardellina, Michael S. Balaschak, Mark R. Alexander, Tanya R. Prather, Robert H. Shoemaker, Micheal R. Boyd Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 2-oxo-18-acetoxy-10¦Á,17¦Á,19¦Á,20¦Â-(-)-cleroda-3,13(16),14-triene C22H32O3 ÏàËÆ¶È:62.5% Phytochemistry 1989 28 2489-2492 Terpenoid and alkaloid compounds from the seeds of Monodora brevipes Joseph T. Etse,Alexander I. Gray,Duncan W. Thomas,Peter G. Waterman Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 2¦Â-acetoxy-isozuelanin-6¦Â-cinnamate ÏàËÆ¶È:62.5% Phytochemistry 1990 29 3591-3595 Clerodane diterpenes from Casearia corymbosa stem bark Mamunur R. Khan,Alexander I. Gray,Ian H. Sadler,Peter G. Waterman Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 3¦Á-Bromomethyl-17-(1',2'-dioxyethyl)androst-5-ene C20H29Br ÏàËÆ¶È:62.5% Steroids 1995 60 699-708 The synthesis and reactivity of 3¦Â-(2-alkynylsulfonyl)- and 3¦Â-(2-alkynylsulfonylmethyl) androst-5-en-17-ones as inhibitors of glucose-6-phosphate dehydrogenase John R. Williams, Jeffrey C. Boehm Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . 3 ¦Á,12¦Á-Dihydroxycholanic acid ÏàËÆ¶È:62.5% Archives of Pharmacal Research 2009 32 857-862 Bile acid derivatives from a sponge-associated bacterium Psychrobacter sp. Huayue Li, Pramod B. Shinde, Hye Ja Lee, Eun Sook Yoo and Chong-O. Lee, et al. Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . 1-Deoxy-3-(1,1-dimethylheptyl)-D9(11)-THC C25H38O ÏàËÆ¶È:62.5% Bioorganic & Medicinal Chemistry 1999 7 2905-2914 3-(1',1'-Dimethylbutyl)-1-deoxy-¦¤8-THC and related compounds: synthesis of selective ligands for the CB2 receptor John W. Huffman, John Liddle, Shu Yu, Mie Mie Aung, Mary E. Abood, Jenny L. Wiley, Billy R. Martin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . (6S,7S,9Z)-nonadeca-9,18-diene-6,7-diol C19H36O2 ÏàËÆ¶È:62.5% Australian Journal of Chemistry 1990 43 895-911 Epoxy Lipids From the Australian Epiphytic Brown Alga Notheia anomala RA Barrow and RJ Capon Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . 9-((1S,2R)-2-((2S,19S,20S)-19-methoxy-20-methyloctatriacontan-2-yl)cyclopropyl)nonan-1-ol C52H104O2 ÏàËÆ¶È:62.5% Tetrahedron 2013 69 6285-6296 The synthesis of methoxy and keto mycolic acids containing methyl-trans-cyclopropanes Gani Koza, Maged Muzael, Richard R. Schubert-Rowles, Cornelia Theunissen, Juma'a R. Al Dulayymi, Mark S. Baird Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . 3,7-dimethylnonadec-9-ene C21H42 ÏàËÆ¶È:62.5% Canadian Journal of Chemistry 1991 69 1100-1106 Stereoselective syntheses of isomers of 3,7-dimethylnonadecane, a sex pheromone of the alfalfa blotch leafminer (Agromyza frontella (Rondani)) David Miller, François Bilodeau, Robert H. Burnell Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . 3,7-dimethylnonadecane ÏàËÆ¶È:62.5% Canadian Journal of Chemistry 1991 69 1100-1106 Stereoselective syntheses of isomers of 3,7-dimethylnonadecane, a sex pheromone of the alfalfa blotch leafminer (Agromyza frontella (Rondani)) David Miller, François Bilodeau, Robert H. Burnell Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . 5-[(3S,7S)-3,7-dimethyltetradecanesulfonyl]-1-phenyl-1H-tetrazole C23H38N4O2S ÏàËÆ¶È:62.5% The Journal of Organic Chemistry 2013 78 5970-5986 Highly Stereocontrolled Total Synthesis of ¦Â-d-Mannosyl Phosphomycoketide: A Natural Product from Mycobacterium tuberculosis Nan-Sheng Li, Louise Scharf, Erin J. Adams, and Joseph A. Piccirilli Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . (3S,7S,11S,15S)-3,7,11,15-tetramethyl-1-decosanol C26H54O ÏàËÆ¶È:62.5% The Journal of Organic Chemistry 2013 78 5970-5986 Highly Stereocontrolled Total Synthesis of ¦Â-d-Mannosyl Phosphomycoketide: A Natural Product from Mycobacterium tuberculosis Nan-Sheng Li, Louise Scharf, Erin J. Adams, and Joseph A. Piccirilli Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 21 . (2R/S,3S,7S)-3,7-dimethyl-2-heptacosanol C29H60O ÏàËÆ¶È:62.5% European Journal of Organic Chemistry 2000 2000 1307-1312 Synthesis of (3S,7S)- and (3S,7S,15S)- Stereoisomers of 3,7-Dimethyl-2-heptacosanone and 3,7,15-Trimethyl-2-heptacosanone, the Ketones Identified from the Locust Schistocerca gregaria Yoshihide Nakamura and Kenji Mori Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 22 . 6-(tert-Butyl)-1,2,3,4-tetrabutylnaphthalene C30H48 ÏàËÆ¶È:62.5% Tetrahedron 2012 68 5167-5171 Iron-catalyzed annulation reaction of arylindium reagents and alkynes to produce substituted naphthalenes Laksmikanta Adak, Naohiko Yoshikai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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