| ²é¿´: 418 | »Ø¸´: 1 | |||
Shen198965гæ (ÖøÃûдÊÖ)
|
[ÇóÖú]
΢Æ×Êý¾ÝÇóÖú»¯ºÏÎï½á¹¹ ÒÑÓÐ1È˲ÎÓë
|
| 13C NMR (75 MHz, CDCl3) ¦Ä12.26,16.56,23.98£¬27.74,28.79,33.50,34.51,38.39,53.73,67.65,69.36,80.83,105.80, 213.20. |
» ²ÂÄãϲ»¶
332Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
²ÄÁϹ¤³Ì085601£¬270Çóµ÷¼Á
ÒѾÓÐ29È˻ظ´
²ÄÁÏÓ뻯¹¤µ÷¼Á
ÒѾÓÐ14È˻ظ´
291 Çóµ÷¼Á
ÒѾÓÐ17È˻ظ´
»úеר˶270Çóµ÷¼Á£¬½ÓÊÜ¿çרҵ
ÒѾÓÐ11È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
±¾¿Æ211 ¹¤¿Æ085400 280·ÖÇóµ÷¼Á ¿É¿çרҵ
ÒѾÓÐ8È˻ظ´
»¯Ñ§¹¤³ÌÓë¼¼Êõ324µ÷¼Á
ÒѾÓÐ23È˻ظ´
²ÄÁÏ085601µ÷¼Á
ÒѾÓÐ15È˻ظ´
269Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×Êý¾ÝÇóÖú¡ª¡ªÈý¸ö»¯ºÏÎï лл£¡
ÒѾÓÐ8È˻ظ´
Õâ¸ö½á¹¹Ê½µÄCASºÅÊǶàÉÙ£¬Ôõô¸ù¾Ý½á¹¹ÕÒCASºÅ
ÒѾÓÐ4È˻ظ´
ÇëÎÊÈçºÎ¸ù¾ÝÇâÆ×̼Æ×Êý¾ÝÍÆ²â»¯ºÏÎï½á¹¹
ÒѾÓÐ6È˻ظ´
¸ù¾Ý½á¹¹¶Ô»¯ºÏÎï½øÐÐÃüÃû
ÒѾÓÐ4È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
Çó¸ßÊÖ£¬ÒÑÖª»¯ºÏÎï½á¹¹Ê½£¬Ôõô²éѯÃû×ÖµÈÏà¹ØÐÅÏ¢
ÒѾÓÐ4È˻ظ´
ÖªµÀ»¯ºÏÎïÃû³ÆÔõô²é»¯ºÏÎïµÄ½á¹¹Ê½£¿
ÒѾÓÐ8È˻ظ´
MestReNovaÎÞ·¨½øÐл¯ºÏÎï½á¹¹ÇâÆ×Ô¤²â
ÒѾÓÐ12È˻ظ´
ÇóÖú£ººìÍâ¹âÆ×·ÖÎö
ÒѾÓÐ7È˻ظ´
ÇóÍÆ¼ö¹ØÓÚ»¯ºÏÎï½á¹¹Óë»îÐÔ¹ØÏµµÄÆÚ¿¯
ÒѾÓÐ4È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú±È½ÏÁ½¸ö½á¹¹ÏàËÆµÄ»¯ºÏÎïµÄ¼«ÐÔ´óС
ÒѾÓÐ4È˻ظ´
ÇóÖúÈçϵÄÁ½¸ö»¯ºÏÎïÈçºÎͨ¹ýÆ×ͼÐÅÏ¢À´È·Ö¤¾ßÌåÊÇÄĸö½á¹¹£¿ лл
ÒѾÓÐ27È˻ظ´
ÔõÑù¸ù¾Ý»¯ºÏÎï½á¹¹Ñ¡ÔñÁ÷¶¯Ïࣿ
ÒѾÓÐ11È˻ظ´
¡¾ÇóÖú¡¿´ÓÒ»¸öÒ©Æ·µÄ´úºÅÔõô²éÕҸû¯ºÏÎïµÄ»¯Ñ§½á¹¹£¿
ÒѾÓÐ13È˻ظ´
¡¾ÇóÖú¡¿Ààú½á¹¹Ä£ÐÍ»¯ºÏÎïµÄÑ¡Ôñ
ÒѾÓÐ8È˻ظ´
¡¾ÇóÖú¡¿ÓÐûÓиßÊÖ¿ÉÒÔ¸ù¾Ý»¯ºÏÎïµÄ½á¹¹ºÍºË´ÅÊý¾Ý×ö³öÏàÓ¦µÄºË´ÅͼÆ×£¿
ÒѾÓÐ9È˻ظ´
¡¾ÇóÖú¡¿ÇóÒ»¸ö»³ö»¯ºÏÎï½á¹¹Ê½À´¼ìË÷ÎÄÏ×µÄÍøÕ¾
ÒѾÓÐ20È˻ظ´
¡¾Çë½Ì¡¿XÉäÏßÑÜÉäÈ·¶¨»¯ºÏÎï½á¹¹
ÒѾÓÐ10È˻ظ´
¡¾ÇóÖú¡¿ÇóÖú-½âÎöHMBC È·¶¨½á¹¹
ÒѾÓÐ13È˻ظ´
seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48426.9
- ºì»¨: 52
- Ìû×Ó: 6748
- ÔÚÏß: 546.4Сʱ
- ³æºÅ: 2400995
- ×¢²á: 2013-04-01
- ÐÔ±ð: MM
- רҵ: ʳƷ¿ÆÑ§»ù´¡
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Shen198965: ½ð±Ò+10 2015-05-15 17:25:47
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Shen198965: ½ð±Ò+10 2015-05-15 17:25:47
|
1 . 4¦Á-hydroxy-homalomenol C C15H26O4 ÏàËÆ¶È:60% Phytochemistry 2009 70 1435-1441 Sesquiterpenoids from Teucrium ramosissimum Hichem Henchiri, Bernard Bodo, Alexandre Deville, Lionel Dubost, Lazhar Zourgui, Aly Raies, Philippe Grellier, Lengo Mambu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . Compound 8 ÏàËÆ¶È:57.1% Bioorganic & Medicinal Chemistry Letters 1993 3 1403-1408 Designing inhibitors of dehydroquinate synthase. Structural simplicity versus inhibitory potency Jean-Luc Montchamp, L. T. Piehler, T. J. Tolbert, J. W. Frost Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . Compound 10ax ÏàËÆ¶È:57.1% Magnetic Resonance in Chemistry 2003 41 554-556 Saturated amine oxides: Part 5. Hydroacridines: Part 24.13C NMR chemical shifts of N-epimeric saturated six-membered azaheterocyclic amine oxides Francisc Potmischil, Valentin Cîmpeanu, Helmut Herzog, Joachim Buddrus and Helmut Duddeck Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . Steperoxide C C14H24O4 ÏàËÆ¶È:57.1% Fitoterapia 2010 81 1205-1207 Two new chamigrane metabolites from fermentation broth of Steccherinum ochraceum Dong-Ze Liu, Ming-He Luo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 2-(1,1-diethyl-1-silapropoxy)-2-(2,2-dimethyl-4-ynyl)cy-clopentan-1-one C18H32O2Si ÏàËÆ¶È:57.1% Tetrahedron 2000 56 9241-9257 The Novel Skeletal Rearrangement of Cyclopentanones into Hydroazulenones via a Radical Process and its Application to the Formal Synthesis of Damsinic Acid Atsushi Nishida, Irie Miyoshi, Yukie Ogasawara, Shinji Nagumo, Norio Kawahara, Mayumi Nishida, Hiroaki Takayanagi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . (2R/S,6R)-(2)-2,6-dimethyl-1-octanol ÏàËÆ¶È:57.1% European Journal of Organic Chemistry 2001 2001 353-363 Syntheses of the Sixteen Stereoisomers of 3,7,11-Trimethyl-2-tridecanol, Including the (2S,3S,7S,11R) and (2S,3S,7S,11S) Stereoisomers Identified as Pheromone Precursors in Females of the Pine Sawfly Microdiprion pallipes (Hymenoptera: Diprionidae) Michael Larsson, Ba-Vu Nguyen, Hans-Erik Högberg and Erik Hedenström Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 5'-hydroxyepijuvabione C16H24O3 ÏàËÆ¶È:56.2% Phytochemistry 1992 31 3773-3780 Occurrence of epijuvabione-type sesquiterpenoids in Abies sachalinensis Atsushi Numata, Kenzo Kawai, Chika Takahashi, Tamie Miyamoto Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 2-isothiocyanato-6-axene C16H25NS ÏàËÆ¶È:56.2% Tetrahedron 2006 62 10393-10399 Stereochemical challenges in characterizing nitrogenous spiro-axane sesquiterpenes from the Indo-Pacific sponges Amorphinopsis and Axinyssa Christopher J. Wegerski, Rachel N. Sonnenschein, Freddy Cabriales, Frederick A. Valeriote, Teatulohi Matainaho, Phillip Crews Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-05-15 11:23:18













»Ø¸´´ËÂ¥