| ²é¿´: 355 | »Ø¸´: 1 | ||
zgzykxyygpͳæ (ÕýʽдÊÖ)
|
[ÇóÖú]
scifinder ½á¹¹¼ìË÷£¨¼±¼±¼±£¬ÔÚÏߵȣ¬Ð»Ð»£©
|
|
ÄÄλ´óÏÀ°ïÎÒÒ»¸ö»¯ºÏÎï²Å²éÐÂÁË£¬£¬¾ÍÊǰïÎÒ²éÒ»ÏÂÕâ¸ö»¯ºÏÎïÊÇ·ñÊÇл¯ºÏÎÈôÊÇÒÑÖª£¬¾Í°ÑÆä»¯ºÏÎï±àºÅºÍÏà¹Ø²Î¿¼ÎÄÏ×·¢¸øÎÒһϣ¬ÈôÊÇл¯ºÏÎ¾Í°Ñǰ10-20¸ö½á¹¹·¢¸øÎÒһϣ¨°´ÏàËÆ¶È¸ßµÍ£© £¬Ð»Ð» 1234.jpg |
» ²ÂÄãϲ»¶
¿¼Ñе÷¼Á-²ÄÁÏÀà-284
ÒѾÓÐ3È˻ظ´
0703»¯Ñ§Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
Ò»Ö¾Ô¸Éî´ó085601²ÄÁϹ¤³Ìרҵ£¨×¨Ë¶£©300·Ö¿ÉÒÔµ÷¼ÁÈ¥ÄÄ
ÒѾÓÐ16È˻ظ´
085801 ×Ü·Ö275 ±¾¿ÆÐÂÄÜÔ´ Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
368»¯Ñ§Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
334Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
085404£¬334·Ö£¬Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
²ÄÁÏר˶µ÷¼Á
ÒѾÓÐ15È˻ظ´
²ÄÁϹ¤³Ìµ÷¼Á
ÒѾÓÐ9È˻ظ´
²ÄÁÏ»¯¹¤×Ü·Ö334Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
Çë½Ì£¬scifinder webÒѾÔËÐÐjavaµ«»¹ÊÇÎÞ·¨»½á¹¹Ê½ºÍ·´Ó¦Ê½£¬ÇóÖú°¡
ÒѾÓÐ13È˻ظ´
ÈçºÎËÑË÷ijһ»¯Ñ§ÎïÖʵÚÒ»´Î±¨µÀ³öÀ´µÄÏà¹ØÎÄÏ×£¿
ÒѾÓÐ4È˻ظ´
scifinder ½á¹¹¼ìË÷£¨¼±¼±¼±£¬ÔÚÏߵȸßÊÖÇë½Ì£©
ÒѾÓÐ3È˻ظ´
ÄÄλºÃÐÄÈ˰ïÎÒÔÚsciFinderÉϼìË÷Ò»ÏÂÎҵϝºÏÎ°ÝлÁË£¡
ÒѾÓÐ4È˻ظ´
ÈçºÎÔÚScifinderÖмìË÷º¬ÓÐÌØ¶¨ÔÓ»·µÄÌìÈ»²úÎï¼°Ò©Îï
ÒѾÓÐ10È˻ظ´
ÌìÈ»²úÎïÌáÈ¡Óë·ÖÀëµÄС²Ë³æÇóÖú----ÈçºÎ²éÎÄÏ×
ÒѾÓÐ7È˻ظ´
¡¾·ÖÏí¡¿ScifinderʹÓÃÊÖ²á¼òÌåÖÐÎİ桾ÒÑËÑË÷ÎÞÖØ¸´¡¿
ÒѾÓÐ182È˻ظ´
»¯Ñ§½á¹¹Ê½¼ìË÷¡¢ÀàËÆËÑË÷
ÒѾÓÐ12È˻ظ´
·¼ÕÁ´¼ ËÄÇâßÁà« ºÏ³ÉÇóÖú
ÒѾÓÐ11È˻ظ´
SciPlanner£º´´½¨×Ô¶¨ÒåµÄºÏ³É·Ïß
ÒѾÓÐ9È˻ظ´
SciFinder Web °æ ½á¹¹¼ìË÷ÔõÓÃÄØ
ÒѾÓÐ10È˻ظ´
¡¾ÌÖÂÛ¡¿¹úÄÚ¹ºÂòscifinderºÍbeilstainµÄѧУ»òÑо¿ËùÓÐÄÄЩ£¿
ÒѾÓÐ4È˻ظ´
¡¾ÇóÖú¡¿Ôõôȷ¶¨Ò»ÖÖÎïÖÊûÈ˺ϳɹý£¿
ÒѾÓÐ13È˻ظ´
³ýÁËSciFinderÒÔÍ⻹ÓбðµÄʲô¿ÉÒÔ»½á¹¹¼ìË÷µÄµØ·½Âð£¿
ÒѾÓÐ3È˻ظ´
scifinderʹÓû¥Öú
ÒѾÓÐ46È˻ظ´
ScifinderʹÓÃÖ¸Äϼ°³£¼ûÎÊÌâ½â¾ö·½·¨¡¾Î³¬Å®Ê¿ÃÀ¹ú»¯Ñ§ÎÄÕªÉç±±¾©´ú±í´¦½²½â¡¿
ÒѾÓÐ36È˻ظ´

fancin
гæ (СÓÐÃûÆø)
- Ó¦Öú: 9 (Ó×¶ùÔ°)
- ½ð±Ò: 32.1
- É¢½ð: 705
- ºì»¨: 6
- Ìû×Ó: 226
- ÔÚÏß: 124.1Сʱ
- ³æºÅ: 1069226
- ×¢²á: 2010-08-04
- רҵ: ÌìȻҩÎﻯѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
zgzykxyygp: ½ð±Ò+14, ¡ï¡ï¡ïºÜÓаïÖú, ÄúºÃ£¬·Ç³£¸ÐлÄúµÄ°ïÖú£¬ÄÜ·ñ°ïÎÒ´øËùËÑË÷µÄ½á¹¹Ò»Æð±£´æÎªPDF¸ñʽ£¬·¢¸øÎÒһϣ¬Ð»Ð» 2012-12-29 12:08:54
zgzykxyygp: ½ð±Ò+1, ¡ï¡ï¡ïºÜÓаïÖú 2013-04-10 13:18:13
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
zgzykxyygp: ½ð±Ò+14, ¡ï¡ï¡ïºÜÓаïÖú, ÄúºÃ£¬·Ç³£¸ÐлÄúµÄ°ïÖú£¬ÄÜ·ñ°ïÎÒ´øËùËÑË÷µÄ½á¹¹Ò»Æð±£´æÎªPDF¸ñʽ£¬·¢¸øÎÒһϣ¬Ð»Ð» 2012-12-29 12:08:54
zgzykxyygp: ½ð±Ò+1, ¡ï¡ï¡ïºÜÓаïÖú 2013-04-10 13:18:13
|
CAS Registry Number: 58728-56-6 C15 H26 O2 1,4-Naphthalenediol, decahydro-1,4a-dimethyl-7-(1-methylethylidene)-, [1R-(1¦Á,4¦Â,4a¦Â,8a¦Á)]- (9CI) 1. Biotransformation of the germacrane epoxides by Cichorium intybusFull Text By Piet, Dennis P.; Schrijvers, Robert; Franssen, Maurice C. R.; de Groot, Aede From Tetrahedron (1995), 51(22), 6303-14. | Language: English, Database: CAPLUS The biotransformation of germacrone-4,5-epoxide, germacrone-1,10-epoxide, isogermacrone-4,5-epoxide, germacrene B-4,5-epoxide and germacrene B-1,10-epoxide by a suspension of fresh chicory root (Cichorium intybus) was investigated. Enzyme-catalyzed cyclizations towards substituted guaianes and eudesmanes were obsd. ~21 2. Medium-ring 1,5-dienes. III. Cyclization of germacra-1(10),4,7(11)-triene oxidesFull Text By Brown, Edward D.; Sutherland, James K.; Sam, Teng W. From Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999) (1975), (22), 2332-6. | Language: English, Database: CAPLUS Epoxidn. of the triene I gave the corresponding 4,5-, 1,10-, and exocyclic epoxides, II-IV, resp. and an explanation was offered for the relative proportions obtained (II > III >> IV). Acid-catalyzed cyclization of II gave guaiane derivs. whereas similar treatment of III gave selinanes. Reductive cyclization of II gave a guaiane and on pyrolysis II was converted into a bicyclo[4.1.0]heptane deriv. having the C skeleton of the carabrone sesquiterpenes. |
2Â¥2012-12-29 11:05:51














»Ø¸´´ËÂ¥