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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

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250350663: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, лл 2014-05-16 17:48:32
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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×Ä£Äâͼ

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4Â¥2014-05-16 14:35:19
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250350663

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ÒýÓûØÌû:
4Â¥: Originally posted by ׿Խ_ÏÈ·æ at 2014-05-16 14:35:19
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 ...

5Â¥2014-05-16 17:48:47
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