| ²é¿´: 311 | »Ø¸´: 1 | ||
zhaocaiguiÒø³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖúÒ»¸ö»¯ºÏÎï½á¹¹£¬Ìؼ±
|
|
13C NMR (101 MHz, CDCl3) ¦Ä 164.07,141.66,138.12,127.73,53.40,50.66,43.39,39.52,37.74,36.16,36.05,23.75,20.66,16.28,11.88 |
» ²ÂÄãϲ»¶
307·Ö²ÄÁÏרҵÇóµ÷¼Á
ÒѾÓÐ10È˻ظ´
304Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
336Çóµ÷¼Á£¬Ò»Ö¾Ô¸Öпƴó
ÒѾÓÐ9È˻ظ´
Çóµ÷¼Á Ò»Ö¾Ô¸Î÷ÄϽ»Í¨´óѧ085701»·¾³¹¤³Ì 282·Ö
ÒѾÓÐ15È˻ظ´
»¯Ñ§¹¤³Ìµ÷¼Á289
ÒѾÓÐ24È˻ظ´
284Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
275 Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
²ÄÁϹ¤³Ì322
ÒѾÓÐ16È˻ظ´
»¯¹¤Ñ§Ë¶ 285Çóµ÷¼Á
ÒѾÓÐ24È˻ظ´
293µ÷¼Á
ÒѾÓÐ18È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú 1,3-¶þôÊ»ù»¯ºÏÎïÏ©´¼½á¹¹ÔÚʲôÌõ¼þÏ¿ÉÒÔת»¯Îª¶þͪʽ
ÒѾÓÐ17È˻ظ´
΢Æ×ÇóÖúÒ»»¯ºÏÎ£¡
ÒѾÓÐ5È˻ظ´
ÔõÑùÓúìÍâÆ×ͼ¶¨ÐÔÅжϻ¯ºÏÎï½á¹¹
ÒѾÓÐ7È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎï΢Æ×Êý¾Ý£¨3£©£¬Ð»Ð»£¡
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯһ¸ö»¯ºÏÎï~¼±~£¡Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ½âÆ×
ÒѾÓÐ20È˻ظ´
scifinder ½á¹¹¼ìË÷£¨¼±¼±¼±£¬ÔÚÏߵȸßÊÖÇë½Ì£©
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»»¯ºÏÎï΢Æ×Êý¾Ý½á¹¹
ÒѾÓÐ3È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖúÒ»¸öÓÃ΢Æ×½âÎöµÄ½á¹¹ 85%ÏàËÆÒ²ÐÐ
ÒѾÓÐ3È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
ºË´Å/ÖÊÆ×½âÆ×¸ßÊÖ°ïæ¿´¿´Õâ¸ö»¯ºÏÎï½á¹¹Ôõô½âÎö
ÒѾÓÐ12È˻ظ´
¡¾ÇóÖú¡¿éÎÆ¤ËغÍÏð»ÆËØÊÇͬһ¸ö»¯ºÏÎï°É£¡¿´½á¹¹Ê½ÊÇÒ»ÑùµÄ°¡£¡Êǹ¹ÐͲîÒìÂð£¿
ÒѾÓÐ6È˻ظ´
¡¾ÇóÖú¡¿´ÓÒ»¸öÒ©Æ·µÄ´úºÅÔõô²éÕҸû¯ºÏÎïµÄ»¯Ñ§½á¹¹£¿
ÒѾÓÐ13È˻ظ´
¡¾ÇóÖú¡¿ÇóÒ»¸ö»³ö»¯ºÏÎï½á¹¹Ê½À´¼ìË÷ÎÄÏ×µÄÍøÕ¾
ÒѾÓÐ20È˻ظ´
wm0629
Ìú¸Ëľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 341 (´óѧÉú)
- ½ð±Ò: 6381.8
- ºì»¨: 3
- Ìû×Ó: 1962
- ÔÚÏß: 77.9Сʱ
- ³æºÅ: 2217415
- ×¢²á: 2013-01-01
- ÐÔ±ð: GG
- רҵ: ÖÐÒ©ÅÚÖÆ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
zhaocaigui: ½ð±Ò+10, ¡ïÓаïÖú 2013-04-02 00:45:59
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
zhaocaigui: ½ð±Ò+10, ¡ïÓаïÖú 2013-04-02 00:45:59
|
1 . 3-Oxo-4,6-androstadien-17¦Â-ol ÏàËÆ¶È:61.1% Steroids 2007 72 360-367 Chemoselective reduction of 1,4,6-cholestatrien-3-one and 1,4,6-androstatriene-3,17-dione by various hydride reagents Eunjeong Kim, Eunsook Ma Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (1R*,5S*)-N-benzyl-7-azaspiro[4.5]decan-1-ol C16H23NO ÏàËÆ¶È:60% Heterocycles 2000 53 115-126 GABA-analogous Spirocyclic Amino Acid Esters, 5. N-Benzyl-7-azaspiro[4.5]decane-1-carboxylates Markus Bendl, Michael Eder, Ingo Langhammer, and Ernst Urban* Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 17¦Â-Hydroxyandrost¦Á-4,6-dien-3-one C19H26O2 ÏàËÆ¶È:57.8% Steroids 2011 76 1317-1330 Hydroxylation of steroids by Fusarium oxysporum, Exophiala jeanselmei and Ceratocystis paradoxa Patrice C. Peart, Kayanne P. McCook, Floyd A. Russell, William F. Reynolds, Paul B. Reese Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 17¦Â-acetoxyandrosta-4,6-dien-3-one ÏàËÆ¶È:57.8% Journal of the Chemical Society, Perkin Transactions 1 1975 1956-1958 13 C nuclear magnetic resonance spectra of some steroidal unsaturated ketones James R. Hanson and Michael Siverns Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 12,14-diacetoxy-13,14,15,16-tetranorlabdan-8¦Á-ol C20H34O5 ÏàËÆ¶È:56.2% Journal of Natural Products 2008 71(6) 1070-1073 Cyclooxygenase (COX)-1 and -2 Inhibitory Labdane Diterpenes from Crassocephalum mannii Mohamed-Elamir F. Hegazy, Shinji Ohta, Fathy F. Abdel-latif,Hazem A. Albadry, Emi Ohta, Paul W Pare#, and Toshifumi Hirata Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . compound 9 C16H24O3 ÏàËÆ¶È:56.2% Tetrahedron 2010 66 5235-5243 New eremophilanes from Farfugium japonicum Motoo Tori, Kanako Otose, Hiroko Fukuyama, Junko Murata, Yasuko Shiotani, Shigeru Takaoka, Katsuyuki Nakashima, Masakazu Sono, Masami Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Methyl erythroxa-3,15-dien-18-oate C21H32O2 ÏàËÆ¶È:55% Phytochemistry 1985 24 611-612 A diterpene related to erythroxydiol from Helichrysum refluxum Ferdinand Bohlmann, Lievy Hartono, Jasmin Jakupovic Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . sinodielide A C15H20O2 ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 2003 51(1) 68-70 Four Guaianolides from Sinodielsia yunnanensis Nian-He WANG,Masahiko TANIGUCHI, Daisuke TSUJI, Mitsunobu DOI,Hirohumi OHISHI, Kenji YOZA,c and Kimiye BABA Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 1,3-dihydroxyeremophila-9,7(11)-dien-8-one ÏàËÆ¶È:53.3% Journal of Natural Products 2003 66 225-229 New Oplopane and Eremophilane Derivatives from Robinsonecio gerberifolius Amira Arciniegas, Ana-L. Prez-Castorena, Sibet Reyes, Jos Luis Contreras, and Alfonso Romo de Vivar Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 1¦Â,4¦Â,4¦Á,5¦Â-diepoxy-10¦Á,11¦ÁH-xantha-12,8¦Â-olide C15H22O4 ÏàËÆ¶È:53.3% Journal of Natural Products 2003 66 1554-1557 Xanthanolides, Germacranolides, and Other Constituents from Carpesium longifolium Chao Yang, Chengshan Yuan, and Zhongjian Jia Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 3 C15H23ClO2 ÏàËÆ¶È:53.3% Journal of Natural Products 2001 64 111-113 New Sesquiterpene Carbonimidic Dichlorides and Related Compounds from the Sponge Stylotella aurantium Musri Musman, Junichi Tanaka, and Tatsuo Higa Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 7¦ÂH-4¦Á,14;11¦Î,12-diepoxyeudesman-3¦Á-ol C15H24O3 ÏàËÆ¶È:53.3% Journal of Natural Products 1998 61 22-28 Enantioselective Total Syntheses of (-)-7¦ÂH-Eudesmane-4¦Á, 11-diol and (+)-ent-7¦ÂH-Eudesmane-4¦Á, 11-diol Fumito Shimoma, Hisao Kondo, Saori Yuuya, Toshio Suzuki, Hisahiro Hagiwara, and Masayoshi Ando Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . clovan-2,9-dione C15H22O2 ÏàËÆ¶È:53.3% Journal of Natural Products 1998 61 1348-1351 The Biotransformation of Some Clovanes by Botrytis cinerea Isidro G. Collado, James R. Hanson, Antonio J. Mac¨ªas-S¨¢nchez, and D. Mobbs Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . trans-5-Methyl-bicyclo[5.3.0]decan-2,8-dion C11H16O2 ÏàËÆ¶È:53.3% Helvetica Chimica Acta 1981 64 736-760 3-Hydroxy-4-nitro-cyclohexanone aus Ketonen und 4-Nitrobuttersäurechlorid. Eine ringerweiternde F¨¹nfringanellierung Thomas Weller, Dieter Seebach, Raymond E. Davis, Brian B. Laird Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 3¦Â-hydroxy-4¦Á,5¦Á,11¦Â-H-eudesman-6¦Á,12-olide C15H24O3 ÏàËÆ¶È:53.3% Journal of Natural Products 1995 Vol 58 1498-1507 Microbial Transformations of 6¦Á- and 6¦Â-Eudesmanolides by Rhizopus nigricans Cultures Yolanda Garc¨ªa, Andr¨¦s Garc¨ªa-Granados, Antonio Mart¨ªnez, Andr¨¦s Parra, Francisco Rivas, Jos¨¦ Mar¨ªa Arias Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 1¦Â,3¦Â-dihydroxy-4¦Â,5¦Á,11-H-eudesman-6¦Á,12-olide C15H24O4 ÏàËÆ¶È:53.3% Journal of Natural Products 1995 Vol 58 1498-1507 Microbial Transformations of 6¦Á- and 6 ¦Â-Eudesmanolides by Rhizopus nigricans Cultures Yolanda Garc¨ªa, Andr¨¦s Garc¨ªa-Granados, Antonio Mart¨ªnez, Andr¨¦s Parra, Francisco Rivas, Jos¨¦ Mar¨ªa Arias Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . critonilide ÏàËÆ¶È:53.3% Phytochemistry 1994 37 1317-1321 Rearranged ent-eudesmane- and ent-eremophilane-type sesquiterpenoids from the liverwort Frullania dilatata Fumihiro Nagashima, Shigeru Takaoka, Siegfried Huneck, Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . zerumbone ÏàËÆ¶È:53.3% Phytochemistry 1988 27 3887-3891 Terpenoids from Curcuma heyneana Kurnia Firman,Takeshi Kinoshita,Akiko Itai,Ushio Sankawa Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . (1R,2R,6R,8R,9R)-9-hydroxy-1,8,12,12-tetramethyl-4-oxatricyclo[6.4.0.02,6]dodecan-3-one C15H24O3 ÏàËÆ¶È:53.3% Indian Journal of Chemistry 2010 49B 776-788 Enantiospecific total synthesis of ent-5-senecioyl-oxy-10,11-epoxythapsan-10-ol A Srikrishna* & K Anebouselvy Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . (-)-Valeranone ÏàËÆ¶È:53.3% Magnetic Resonance in Chemistry 2004 42 898-902 DFT and NMR parameterized conformation of valeranone J. Mart¨ªn Torres-Valencia, Myriam Mel¨¦ndez-Rodr¨ªguez, Roc¨ªo ¨¢lvarez-Garc¨ªa, Carlos M. Cerda-Garc¨ªa-Rojas and Pedro Joseph-Nathan Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . Bis[(2R)-2,5,5-trimethylbicyclo[2.2.1]hept-2-ylcyclopentadienyl]dichlorotitanium(IV) C30H34Cl2Ti ÏàËÆ¶È:53.3% Zeitschrift f¨¹r Naturforschung B 2009 64 25-40 Formation of Quaternary Stereogenic Centers by Wagner-Meerwein Rearrangement - Synthesis of Optically Active Cyclopentadienyl Complexes from Borneol and Fenchol C. Färber, G. Wolmershäuser, and H. Sitzmann Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . (1S*,2R*,3R*,4R*)-3-(Benzylthio)-2-carboxybicyclo[2.2.1]heptan-2-aminium chloride C15H20ClNO2S ÏàËÆ¶È:53.3% Tetrahedron 2012 68 1951-1962 Sulfanyl-methylene-5(4H)-oxazolones and ¦Â-sulfanyl-¦Á-nitroacrylates as appealing dienophiles for the synthesis of conformationally constrained cysteine analogues Alessandro Ruffoni, Alessandro Casoni, Sara Pellegrino, Maria Luisa Gelmi, Raffaella Soave, Francesca Clerici Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . (¡À)-valeranone ÏàËÆ¶È:53.3% Bulletin of the Chemical Society of Japan 1993 66 2694-2699 Synthetic Photochemistry. LXI. A Total Synthesis of (¡À)-Valeranone, a cis-Decalone Sesquiterpenoid from Valeriana officinalis, via an Intramolecular Photocycloaddition Hitoshi Takeshita, Ying-She Cui, Nobuo Kato, Akira Mori Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . (-)-5R,6R-microcionin-2 ÏàËÆ¶È:53.3% Tetrahedron 2005 61 11032-11037 Pelseneeriol-1 and -2: new furanosesquiterpene alcohols from porostome nudibranch Doriopsilla pelseneeri Helena Gaspar, Margherita Gavagnin, Gonçalo Calado, Francesco Castelluccio, Ernesto Mollo, Guido Cimino Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . compound 9 C14H22O ÏàËÆ¶È:53.3% Tetrahedron 2000 56 1655-1659 Isolation and Structure of Striatenic Acid from Liverwort Cheilolejeunea serpentina and the Absolute Configuration by Synthesis Motoo Tori, Akihito Aiba, Hiroki Koyama, Toshihiro Hashimoto, Katsuyuki Nakashima, Masakazu Sono, Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . 3,11-cadinadiene C15H24 ÏàËÆ¶È:53.3% Tetrahedron 1999 55 15099-15108 Synthesis of amorphane and cadinane sesquiterpenes from fabiana imbricata Koon-Sin Ngo, Geoffrey D. Brown Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-04-01 07:48:15














»Ø¸´´ËÂ¥