| ²é¿´: 347 | »Ø¸´: 2 | ||
chumjunгæ (ÕýʽдÊÖ)
|
[ÇóÖú]
CÆ×ÇóÖú»¯ºÏÎï½á¹¹ ÒÑÓÐ2È˲ÎÓë
|
|
ë®´úÈܼÁ£ºDMSO CÆ×Êý¾Ý£º14.4,20.0,22.6,23.6,26.8,29.0,29.2,29.3,29.4,29.7,30.1,30.3,31.6,31.7,32.5,34.7,34.9,36.8,43.2,118.9,124.6,124.7,138.3,138.4,147.4,147.5,147.6,209 |
» ²ÂÄãϲ»¶
329Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
¸´ÊÔµ÷¼Á
ÒѾÓÐ4È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ10È˻ظ´
292Çóµ÷¼Á
ÒѾÓÐ11È˻ظ´
Ò»Ö¾Ô¸211£¬»¯Ñ§Ñ§Ë¶£¬310·Ö£¬±¾¿ÆÖصãË«·Ç£¬Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
363Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
0703×Ü·Ö331Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
²ÄÁÏר˶(0856) 339·ÖÇóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
»¯ºÏÎïµÄ¾ßÌå½á¹¹
ÒѾÓÐ3È˻ظ´
ºÏ³É»¯ºÏÎïµÄÇâÆ×»ý·Ö±ÈÀý²»¶Ôµ«Êǵ¥¾§½á¹¹ÏÔʾµÃµ½Á˸û¯ºÏÎï£¬ÌØÏò¸÷λ´óÉñÇóÖú¡£
ÒѾÓÐ16È˻ظ´
ʲôÆ×ͼÄÜÈ·ÈÏ»¯ºÏÎïµÄ½á¹¹
ÒѾÓÐ9È˻ظ´
ÔÚÄĸöÍøÕ¾¿ÉÒԲ鵽»¯ºÏÎïµÄͼÆ×
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú1¸ö»¯ºÏÎï
ÒѾÓÐ3È˻ظ´
ÇëÎÊÈçºÎ¸ù¾ÝÇâÆ×̼Æ×Êý¾ÝÍÆ²â»¯ºÏÎï½á¹¹
ÒѾÓÐ6È˻ظ´
»¯ºÏÎï×öH-NMRÆ×º¬µãÔÓÖÊÄܲ»ÄÜ×ö
ÒѾÓÐ6È˻ظ´
Çó΢ÆÕ½âÎö»¯ºÏÎï½á¹¹
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖúÓÃCDÆ×½âÎöÒ»¸öÄ¾Ö¬ËØÀ໯ºÏÎïµÄ¾ø¶Ô¹¹ÐÍ
ÒѾÓÐ7È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
»¯ºÏÎïµÄ½âÆ× Óк˴ÅͼÆ× ÓÐÖÊÆ×ͼ ºÜ¹îÒìµÄ»¯ºÏÎï Á¬Ê²Ã´ÀàÐ͵ͼÅб𲻳ö ÌØ´ËÇóÖú
ÒѾÓÐ25È˻ظ´
ÇóÖú½âÎöÒ»»¯ºÏÎïµÄHÆ×CÆ×£¬¸½ÉÏͼÆ×
ÒѾÓÐ13È˻ظ´
¡¾ÇóÖú¡¿·ÖÀëÌá´¿µÃµ½µÄ»¯ºÏÎï¼òµ¥ÇâÆ×ºÍ̼Æ×½âÎö
ÒѾÓÐ10È˻ظ´
ÇëÎÊÓÐûÓÐÒ»¸ö»¯ºÏÎï±ê×¼Æ×ͼ½âÎöÊý¾Ý¿â£¿
ÒѾÓÐ5È˻ظ´
ÇóÖú HÆ×ºÍCÆ×
ÒѾÓÐ15È˻ظ´
¡¾ÇóÖú¡¿Çë³æÓÑÃǰï°ï½âÒ»ÏÂÕâ¸ö»¯ºÏÎï°¡£¬ÓÐÇâÆ×£¬Ì¼Æ×ºÍÖÊÆ×Êý¾Ý
ÒѾÓÐ9È˻ظ´
¡¾ÇóÖú¡¿ÇóÖú½âÆ×CÆ×ºÍHÆ×
ÒѾÓÐ22È˻ظ´
¡¾ÇóÖú¡¿¸÷λºÃ£¬ÇëÎÒ¿´Ò»¸ö¼òµ¥»¯ºÏÎïµÄHNMRÆ×ͼ¡£
ÒѾÓÐ20È˻ظ´
¡¾ÇóÖú¡¿¸ù¾ÝMSºÍ1H NMRÆ×ͼȷ¶¨»¯ºÏÎï
ÒѾÓÐ11È˻ظ´
¡¾ÇóÖú¡¿ÇóÖú-½âÎöHMBC È·¶¨½á¹¹
ÒѾÓÐ13È˻ظ´
yangyinhe
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1566 (½²Ê¦)
- ½ð±Ò: 15048.4
- ºì»¨: 21
- Ìû×Ó: 2773
- ÔÚÏß: 261.2Сʱ
- ³æºÅ: 942922
- ×¢²á: 2010-01-15
- ÐÔ±ð: MM
- רҵ: ÌìÈ»Óлú»¯Ñ§
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
|
1 . 5,13-Dimethyl-1,5-heptadecadiene ÏàËÆ¶È:65.5% Bioscience, Biotechnology, and Biochemistry 2009 73 1618-1622 Synthesis and Field Evaluation of Methyl-branched Ketones, Sex Pheromone Components Produced by Lithosiinae Female Moths in the Family of Arctiidae Nguyen Duc DO, Masakatsu KINJO, Tomonori TAGURI, Yasushi ADACHI, Rei YAMAKAWA and Tetsu ANDO Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 2¦Â-(diundecylamino)-5¦Á-androstane-3¦Á,17¦Â-diol C41H77NO2 ÏàËÆ¶È:65.5% Bioorganic & Medicinal Chemistry 2008 16 5062-5077 Chemical synthesis of 2¦Â-amino-5¦Á-androstane-3¦Á,17¦Â-diol N-derivatives and their antiproliferative effect on HL-60 human leukemia cells Dominic Thibeault, Jenny Roy, Patrick DeRoy, Donald Poirier Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 3-decyl-5,7-dimethyl-2-undecylquinoline C32H53N ÏàËÆ¶È:64.2% Journal of Heterocyclic Chemistry 2004 41 423-429 Ruthenium-catalyzed formal alkyl group transfer: Synthesis of quinolines from nitroarenes and alkylammonium halides Chan Sik Cho,Na Young Lee,Tae-Jeong Kim and Sang Chul Shim Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 2¦Â-(dinonylamino)-5¦Á-androstane-3¦Á,17¦Â-diol C37H69NO2 ÏàËÆ¶È:60.7% Bioorganic & Medicinal Chemistry 2008 16 5062-5077 Chemical synthesis of 2¦Â-amino-5¦Á-androstane-3¦Á,17¦Â-diol N-derivatives and their antiproliferative effect on HL-60 human leukemia cells Dominic Thibeault, Jenny Roy, Patrick DeRoy, Donald Poirier Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 2-(hexadecylsulfanyl)-3-(pentylsulfanyl)-1,4-naphthoquinone C31H48O2S2 ÏàËÆ¶È:60.7% Russian Journal of Organic Chemistry 2010 46 209-215 Synthesis and spectral properties of 1,4-naphthoquinone sulfanyl derivatives C. Sayil and C. Ibis Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 2-(butylsulfanyl)-3-(hexadecylsulfanyl)-1,4-naphthoquinone C30H46O2S2 ÏàËÆ¶È:60.7% Russian Journal of Organic Chemistry 2010 46 209-215 Synthesis and spectral properties of 1,4-naphthoquinone sulfanyl derivatives C. Sayil and C. Ibis Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . compound 18 C112H164O4N4 ÏàËÆ¶È:60.7% European Journal of Organic Chemistry 2011 3016-3025 C4-Symmetric Alkoxyresorcin[4]arene Triflates: The Use of Palladium-Catalyzed Reactions in the Synthesis of Axially Chiral Derivatives with Amino- and/or Alkoxy-Substituents Philip C. Bulman Page, Terence R. Bygrave, Yohan Chan, Harry Heaney and Vickie McKee Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . compound 20 C100H164O4N4 ÏàËÆ¶È:60.7% European Journal of Organic Chemistry 2011 3016-3025 C4-Symmetric Alkoxyresorcin[4]arene Triflates: The Use of Palladium-Catalyzed Reactions in the Synthesis of Axially Chiral Derivatives with Amino- and/or Alkoxy-Substituents Philip C. Bulman Page, Terence R. Bygrave, Yohan Chan, Harry Heaney and Vickie McKee Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . (2S,3S)-2-(13-Bromotridecyl)-3-((R)-1-methylheptadecyl)oxirane C33H65BrO ÏàËÆ¶È:60.7% Tetrahedron 2014 70 7322-7335 Synthetic epoxy-mycolic acids Dakhil Z. Al Kremawi, Juma'a R. Al Dulayymi, Mark S. Baird Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . Bullatacinone ÏàËÆ¶È:60% Journal of Natural Products 1989 Vol 52 463 Bullatacin and Bullatacinone: Two Highly Potent Bioactive Acetogenins from Annona bullata Y.-H. Hui, J. K. Rupprecht, Y. M. Liu, J. E. Anderson, D. L. Smith, C.-J. Chang, J. L. McLaughlin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2015-01-28 16:08:06
lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48805.6
- É¢½ð: 890
- ºì»¨: 208
- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
chumjun: ½ð±Ò+10, ¡ïÓаïÖú 2015-01-29 09:43:47
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
chumjun: ½ð±Ò+10, ¡ïÓаïÖú 2015-01-29 09:43:47
|
²éѯ½á¹û£º¹²²éµ½601¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 5,13-Dimethyl-1,5-heptadecadiene ÏàËÆ¶È:65.5% Bioscience, Biotechnology, and Biochemistry 2009 73 1618-1622 Synthesis and Field Evaluation of Methyl-branched Ketones, Sex Pheromone Components Produced by Lithosiinae Female Moths in the Family of Arctiidae Nguyen Duc DO, Masakatsu KINJO, Tomonori TAGURI, Yasushi ADACHI, Rei YAMAKAWA and Tetsu ANDO Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 2¦Â-(diundecylamino)-5¦Á-androstane-3¦Á,17¦Â-diol C41H77NO2 ÏàËÆ¶È:65.5% Bioorganic & Medicinal Chemistry 2008 16 5062-5077 Chemical synthesis of 2¦Â-amino-5¦Á-androstane-3¦Á,17¦Â-diol N-derivatives and their antiproliferative effect on HL-60 human leukemia cells Dominic Thibeault, Jenny Roy, Patrick DeRoy, Donald Poirier Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 3-decyl-5,7-dimethyl-2-undecylquinoline C32H53N ÏàËÆ¶È:64.2% Journal of Heterocyclic Chemistry 2004 41 423-429 Ruthenium-catalyzed formal alkyl group transfer: Synthesis of quinolines from nitroarenes and alkylammonium halides Chan Sik Cho,Na Young Lee,Tae-Jeong Kim and Sang Chul Shim Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 2¦Â-(dinonylamino)-5¦Á-androstane-3¦Á,17¦Â-diol C37H69NO2 ÏàËÆ¶È:60.7% Bioorganic & Medicinal Chemistry 2008 16 5062-5077 Chemical synthesis of 2¦Â-amino-5¦Á-androstane-3¦Á,17¦Â-diol N-derivatives and their antiproliferative effect on HL-60 human leukemia cells Dominic Thibeault, Jenny Roy, Patrick DeRoy, Donald Poirier Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 2-(hexadecylsulfanyl)-3-(pentylsulfanyl)-1,4-naphthoquinone C31H48O2S2 ÏàËÆ¶È:60.7% Russian Journal of Organic Chemistry 2010 46 209-215 Synthesis and spectral properties of 1,4-naphthoquinone sulfanyl derivatives C. Sayil and C. Ibis Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 2-(butylsulfanyl)-3-(hexadecylsulfanyl)-1,4-naphthoquinone C30H46O2S2 ÏàËÆ¶È:60.7% Russian Journal of Organic Chemistry 2010 46 209-215 Synthesis and spectral properties of 1,4-naphthoquinone sulfanyl derivatives C. Sayil and C. Ibis Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 18 C112H164O4N4 ÏàËÆ¶È:60.7% European Journal of Organic Chemistry 2011 3016-3025 C4-Symmetric Alkoxyresorcin[4]arene Triflates: The Use of Palladium-Catalyzed Reactions in the Synthesis of Axially Chiral Derivatives with Amino- and/or Alkoxy-Substituents Philip C. Bulman Page, Terence R. Bygrave, Yohan Chan, Harry Heaney and Vickie McKee Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 20 C100H164O4N4 ÏàËÆ¶È:60.7% European Journal of Organic Chemistry 2011 3016-3025 C4-Symmetric Alkoxyresorcin[4]arene Triflates: The Use of Palladium-Catalyzed Reactions in the Synthesis of Axially Chiral Derivatives with Amino- and/or Alkoxy-Substituents Philip C. Bulman Page, Terence R. Bygrave, Yohan Chan, Harry Heaney and Vickie McKee Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . (2S,3S)-2-(13-Bromotridecyl)-3-((R)-1-methylheptadecyl)oxirane C33H65BrO ÏàËÆ¶È:60.7% Tetrahedron 2014 70 7322-7335 Synthetic epoxy-mycolic acids Dakhil Z. Al Kremawi, Juma'a R. Al Dulayymi, Mark S. Baird Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . Bullatacinone ÏàËÆ¶È:60% Journal of Natural Products 1989 Vol 52 463 Bullatacin and Bullatacinone: Two Highly Potent Bioactive Acetogenins from Annona bullata Y.-H. Hui, J. K. Rupprecht, Y. M. Liu, J. E. Anderson, D. L. Smith, C.-J. Chang, J. L. McLaughlin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 9-((1R,2R)-2-((2S,19S,20S)-19-methoxy-20-methyloctatriacontan-2-yl)cyclopropyl)nonanal C52H102O2 ÏàËÆ¶È:60% 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 12 . abiet¦Á-8,11,13-trien-18-yl hexadecanoate C36H60O2 ÏàËÆ¶È:59.3% Phytochemistry 2008 69 498-505 Diterpene constituents of leaves from Juniperus brevifolia Ana M.L. Seca, Artur M.S. Silva, Isabel L. Bazzocchi, Ignacio A. Jimenez Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . 5,13-Dimethyl-5-heptadecen-1-ol ÏàËÆ¶È:58.6% Bioscience, Biotechnology, and Biochemistry 2009 73 1618-1622 Synthesis and Field Evaluation of Methyl-branched Ketones, Sex Pheromone Components Produced by Lithosiinae Female Moths in the Family of Arctiidae Nguyen Duc DO, Masakatsu KINJO, Tomonori TAGURI, Yasushi ADACHI, Rei YAMAKAWA and Tetsu ANDO Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . palmitate C36H70O2 ÏàËÆ¶È:58.6% Natural Product Communications 2011 6 767-772 Lipophilic Components from the Ecuadorian Plant Schistocarpha eupatorioides Gianluca Gilardoni, Solveig Tosi, Giorgio Mellerio, Maria Elena Maldonado, Ximena Chiriboga and Giovanni Vidari Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . 2¦Â-(n-dodecylamino)-5¦Á-androstane-3¦Á,17¦Â-diol C31H57NO2 ÏàËÆ¶È:58.0% Bioorganic & Medicinal Chemistry 2008 16 5062-5077 Chemical synthesis of 2¦Â-amino-5¦Á-androstane-3¦Á,17¦Â-diol N-derivatives and their antiproliferative effect on HL-60 human leukemia cells Dominic Thibeault, Jenny Roy, Patrick DeRoy, Donald Poirier Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . 6-decyl-2-hydroxyazulene C20H28O ÏàËÆ¶È:58.0% Tetrahedron 2013 69 4259-4269 Efficient synthesis and redox behavior of a series of 6-alkyl-2-phenylazulenes Shunji Ito, Mao Ueda, Ryuta Sekiguchi, Jun Kawakami Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . (2¦Â,4a¦Â)-1-{2-(8-amino-2,3,4,4a-tetrahydro-6-nonylpyrimido[3,4-b][1,2]oxazinyl)}-2-undecanone C27H49N3O2 ÏàËÆ¶È:57.1% Journal of Natural Products 1999 62 1707-1711 Revision of the Stereochemistry of Batzelladine F. Approaches to the Tricyclic Hydroxyguanidine Moiety of Batzelladines G, H, and I Barry B. Snider and Marina V. Busuyek Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . Termitomycamide C C28H44N2O3 ÏàËÆ¶È:57.1% Organic Letters 2010 Vol.12,No.21 5012-5015 Termitomycamides A to E, Fatty Acid Amides Isolated from the Mushroom Termitomyces titanicus, Suppress Endoplasmic Reticulum Stress Jae-Hoon Choi,Kohei Maeda,Kaoru Nagai, Etsuko Harada, Mitsuo Kawade,Hirofumi Hirai, and Hirokazu Kawagishi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . brachystine C23H41NO ÏàËÆ¶È:57.1% Phytochemistry 1988 27 3523-3527 Minor amides of Piper species S.K. Koul,S.C. Taneja,V.K. Agarwal,K.L. Dhar Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . 2,3,4,5-Tetra(5-dodecylthiophen-2-yl)thiophene C68H108S5 ÏàËÆ¶È:57.1% Tetrahedron 2012 68 1192-1197 Synthesis and characterization of new planar butterfly-shaped fused oligothiophenes Jing Wang, Huan Xu, Bin Li, Xiao-Ping Cao, Hao-Li Zhang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
3Â¥2015-01-28 16:09:24














»Ø¸´´ËÂ¥