| ²é¿´: 319 | »Ø¸´: 1 | ||
ÍðÈçÇåÌÀ½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
άÆÕÇóÖú£¬Ð»Ð»~~ ÒÑÓÐ1È˲ÎÓë
|
|
ÈܼÁΪ뮴ú¼×´¼ 21.3,23.1,33.1,34.1,43.6,45.2,45.9,48.1,99.9,113.0,115.3,132.7,144.2,160.5,163.2 |
» ²ÂÄãϲ»¶
Ò»Ö¾Ô¸»ªÄÏʦ·¶´óѧ0702ÎïÀíѧ305µ÷¼Á
ÒѾÓÐ5È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ30È˻ظ´
266Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
297Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
326·Ö£¬Ò»Ö¾Ô¸»¦9£¬ÇóÉúÎïѧµ÷¼Á
ÒѾÓÐ4È˻ظ´
288Çóµ÷¼Á£¬Ò»Ö¾Ô¸»ªÄÏÀí¹¤´óѧ071005
ÒѾÓÐ3È˻ظ´
304Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
µ÷¼Á
ÒѾÓÐ18È˻ظ´
293µ÷¼Á
ÒѾÓÐ4È˻ظ´
338Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
άÆÕÇóÖú£¬Ð»Ð»~~
ÒѾÓÐ3È˻ظ´
άÆÕÇóÖú£¬Ð»Ð»à¸£¡
ÒѾÓÐ3È˻ظ´
HETEROCYCLESͶ¸åÇóÖú
ÒѾÓÐ9È˻ظ´
άÆÕÇóÖú£¡Ð»Ð»~
ÒѾÓÐ3È˻ظ´
ÄÄÓпÉÒÔÓõÄÇÅÁºÍâÎÄÎÄÏ×°¡¡£ÇóÖú£¡£¡ÖªÍøµÄ²»ÄÜÏÂÔØ°¡£¬ÓÐûÆäËûÇþµÀ£¡
ÒѾÓÐ14È˻ظ´
άÆÕÊý¾ÝÇóÖúX
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»df12
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú£¬ÔÚÏßµÈ
ÒѾÓÐ4È˻ظ´
¼±ÐèάÆÕ̼Æ×¼ìË÷£¬¼±Óã¡Ð»Ð»´ó¼Ò°ïæ
ÒѾÓÐ5È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú3¸ö΢ÆÕÊý¾Ý
ÒѾÓÐ5È˻ظ´
Çó×ö·ÂÒ©Ñõ»¯½µ½âÔÓÖʵķ½·¨¡£
ÒѾÓÐ20È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄάÆÕCÆ×Êý¾Ý~~~~ллÁË~~~~~
ÒѾÓÐ3È˻ظ´
ÇóÖú£º¹ØÓÚÔËË㸴ÔӶȵļÆË㣬лл´ó¼ÒÁË£¡
ÒѾÓÐ3È˻ظ´
ÇëÎÊũѧÀàºËÐÄÆÚ¿¯Éó¸åʱ¼ä£¿Â¼ÓÃ֪ͨҪ¶à¾Ã£¿
ÒѾÓÐ6È˻ظ´
RUSSIAN CHEMICAL BULLETIN
ÒѾÓÐ5È˻ظ´
½Ì½ÌÎÒÈçºÎʹÓÃάÆÕ
ÒѾÓÐ8È˻ظ´
¡¾ÇóÖú¡¿WO3±¡Ä¤µÄÖÆ±¸
ÒѾÓÐ5È˻ظ´

·çÐÐÕß007
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1309 (½²Ê¦)
- ½ð±Ò: 12672.8
- ºì»¨: 15
- Ìû×Ó: 1490
- ÔÚÏß: 299.5Сʱ
- ³æºÅ: 2542465
- ×¢²á: 2013-07-12
- ÐÔ±ð: GG
- רҵ: ÓлúºÏ³É
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ÍðÈçÇåÌÀ: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-05-25 15:29:19
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ÍðÈçÇåÌÀ: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-05-25 15:29:19
|
²éѯ½á¹û£º¹²²éµ½5¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . pyridoxatin (minor) C15H21NO3 ÏàËÆ¶È:93.3% The Journal of Antibiotics 1991 44 685-687 ISOLATION AND STRUCTURAL ELUCIDATION OF PYRIDOXATIN, A FREE RADICAL SCAVENGER OF MICROBIAL ORIGIN YOSHIHIRO TESHIMA, KAZUO SHIN-YA, AKIRA SHIMAZU, KEIKO FURIHATA, HA SANG CHUL, KAZUO FURIHATA, YOICHI HAYAKAWA, KAZUO NAGAI, HARUO SETO Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . pyridoxatin ÏàËÆ¶È:93.3% Marine Drugs 2014 12 1208-1219 Two New Antibiotic Pyridones Produced by a Marine Fungus, Trichoderma sp. Strain MF106 Bin Wu, Vanessa Oesker, Jutta Wiese, Rolf Schmaljohann and Johannes F. Imhoff Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . pyridoxatin (major) C15H21NO3 ÏàËÆ¶È:86.6% The Journal of Antibiotics 1991 44 685-687 ISOLATION AND STRUCTURAL ELUCIDATION OF PYRIDOXATIN, A FREE RADICAL SCAVENGER OF MICROBIAL ORIGIN YOSHIHIRO TESHIMA, KAZUO SHIN-YA, AKIRA SHIMAZU, KEIKO FURIHATA, HA SANG CHUL, KAZUO FURIHATA, YOICHI HAYAKAWA, KAZUO NAGAI, HARUO SETO Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . conocenol A C15H26O3 ÏàËÆ¶È:53.3% Journal of Natural Products 2007 70 1503-1506 Sesquiterpenes from Cultures of the Basidiomycete Conocybe siliginea Dong-Ze Liu,Fei Wang, and Ji-Kai Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 38 ÏàËÆ¶È:53.3% Magnetic Resonance in Chemistry 1987 25 1012-1018 13C NMR spectral data of some N-vanillyl-, N-piperonyl- and N-veratryl-alkylaminoalkylamides Alicia Baldessari and Eduardo G. Gros Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-05-25 14:25:06














»Ø¸´´ËÂ¥