| ²é¿´: 237 | »Ø¸´: 1 | ||
µØ¹ÏµØ¹Ï½ð³æ (³õÈëÎÄ̳)
|
[ÇóÖú]
΢Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë
|
| DMSO-d6:C13: 11.19,16.91,26.58,28.42,28.61,34.28,34.84,35.16,37.99,46.68,52.08,69.19,129.12,161.31,197.22 |
» ²ÂÄãϲ»¶
0703×Ü·Ö331Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
085600£¬321·ÖÇóµ÷¼Á
ÒѾÓÐ7È˻ظ´
325Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
085600£¬320·ÖÇóµ÷¼Á
ÒѾÓÐ12È˻ظ´
Ò»Ö¾Ô¸0817»¯Ñ§¹¤³ÌÓë¼¼Êõ£¬Çóµ÷¼Á
ÒѾÓÐ27È˻ظ´
Ò»Ö¾Ô¸±±¾©»¯¹¤085600 310·ÖÇóµ÷¼Á
ÒѾÓÐ8È˻ظ´
Ò»Ö¾Ô¸¹þ¶û±õ¹¤Òµ´óѧ085600Ó¢Ò»Êý¶þ337·ÖÇóµ÷¼Á
ÒѾÓÐ10È˻ظ´
22408Çóµ÷¼Á 354·Ö ¿É¿çרҵ
ÒѾÓÐ3È˻ظ´
277¹¤¿ÆÇóµ÷¼Á
ÒѾÓÐ4È˻ظ´
Ò»Ö¾Ô¸»¦9£¬ÇóÉúÎïѧµ÷¼Á£¬326·Ö
ÒѾÓÐ3È˻ظ´
seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48394.9
- ºì»¨: 52
- Ìû×Ó: 6742
- 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
µØ¹ÏµØ¹Ï: ½ð±Ò+10, ¡ïÓаïÖú 2015-03-21 16:20:14
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
µØ¹ÏµØ¹Ï: ½ð±Ò+10, ¡ïÓаïÖú 2015-03-21 16:20:14
|
1 . Isodehydrochamaecynone C14H16O ÏàËÆ¶È:60% Journal of Natural Products 2003 66 588-594 Synthetic Approach to Exo-Endo Cross-Conjugated Cyclohexadienones and Its Application to the Syntheses of Dehydrobrachylaenolide,Isodehydrochamaecynone, and trans-Isodehydrochamaecynone Yohsuke Higuchi, Fumito Shimoma, Rei Koyanagi, Kouji Suda,Tomokazu Mitsui, Takao Kataoka, Kazuo Nagai, and Masayoshi Ando Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 1¦Â-hydroxy-¦Á-cyperone ÏàËÆ¶È:60% China Journal of Chinese Materia Medica 2010 35 315-322 Terpenoids of Heteroplexis micocephala and their bioactivities FAN Xiaona; LIN Sheng; ZHU Chenggen; HU Jinfeng; LIU Yang; CHEN Xiaoguang; CHEN Naihong; WANG Wenjie; SHI Jiangong Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Anhuienosol C15H22O2 ÏàËÆ¶È:60% Fitoterapia 2013 86 100-107 Cytotoxic sesquiterpenes from Hedychium spicatum: Isolation, structure elucidation and structure¨Cactivity relationship studies G. Suresh, B. Poornima, K. Suresh Babu, P. Ashok Yadav, M. Suri Appa Rao, Bandi Siva, K. Rajendra Prasad, V. Lakshma Nayak, Sistla Ramakrishna Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 5-Isothiocyanatopupukeanane ÏàËÆ¶È:60% The Journal of Organic Chemistry 1989 54 5184-5186 5-Isothiocyanatopupukeanane from a sponge of the genus Axinyssa Andrew H. Marcus, Tadeusz F. Molinski, Eoin Fahy, D. John Faulkner, Changfu Xu, Jon Clardy Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (3S,3aS,5R,8S,8aS)-5-(2-Hydroxypropan-2-yl)-3,8-dimethyloctahydroazulen-3a(1H)-ol ÏàËÆ¶È:60% Journal of Natural Products 2014 77 2522-2536 Synthesis of Guaia-4(5)-en-11-ol, Guaia-5(6)-en-11-ol, Aciphyllene, 1-epi-Melicodenones C and E, and Other Guaiane-Type Sesquiterpenoids via the Diastereoselective Epoxidation of Guaiol An-Cheng Huang, Christopher J. Sumby, Edward R. T. Tiekink, and Dennis K. Taylor Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (E)-¦Á-Santalyl formate C16H24O2 ÏàËÆ¶È:56.2% Molecules 2012 17 2259-2270 Structure-Odor Relationships of ¦Á-Santalol Derivatives with Modified Side Chains Toshio Hasegawa , Hiroaki Izumi , Yuji Tajima and Hideo Yamada Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 20 C16H29NO3 ÏàËÆ¶È:56.2% Canadian Journal of Chemistry 1996 74 2434-2443 A revised structure for the piperidine alkaloid andrachamine Sibel Mill, Claude Hootel¨¦ Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 8-(tert-butyldiphenylsilyloxy)-(3S,7R)-3,7-dimethyl-octanal C26H38O2Si ÏàËÆ¶È:56.2% 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 ̼Æ×Ä£Äâͼ 9 . 4-Azapregna-16,20-dien-3-one C20H29ON ÏàËÆ¶È:55% Steroids 1995 60 812-816 Palladium-catalyzed homogeneous coupling reactions of steroids with organostannanes Rita Skoda-Földes, Zita Cs¨¢kai, L¨¢szlo Koll¨¢r, Judit Horv¨¢th, Zolt¨¢n Tuba Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-01-28 10:11:13














»Ø¸´´ËÂ¥