| ²é¿´: 418 | »Ø¸´: 1 | ||
¿ÓµùÒ©»¯Ìú³æ (³õÈëÎÄ̳)
|
[ÇóÖú]
΢Æ×ÇóÖú£¬¼±¼±¼±£¡£¡£¡£¡ ÒÑÓÐ1È˲ÎÓë
|
| CÆ×Êý¾Ý£º12.09, 16.69,23.32,23.70,24.36,24.75,24.89,25.27,25.40, 26.93,45.95,46.53,47.41,56.20,94.99,106.56,107.41,114.44,155.67, 158.59,163.13,167.84, 198.76,211.35,212.33 |
» ²ÂÄãϲ»¶
²ÄÁÏÓ뻯¹¤Ò»Ö¾Ô¸Äϲý´óѧ327Çóµ÷¼ÁÍÆ¼ö
ÒѾÓÐ8È˻ظ´
0703 ÎïÀí»¯Ñ§µ÷¼Á
ÒѾÓÐ5È˻ظ´
»¯Ñ§¹¤³Ì321·ÖÇóµ÷¼Á
ÒѾÓÐ7È˻ظ´
0703»¯Ñ§µ÷¼Á 290·ÖÓпÆÑоÀú£¬ÂÛÎÄÔÚͶ
ÒѾÓÐ7È˻ظ´
308Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
±¾ÈË¿¼085602 »¯Ñ§¹¤³Ì ר˶
ÒѾÓÐ10È˻ظ´
½¹ÂÇ
ÒѾÓÐ9È˻ظ´
0856Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
283Çóµ÷¼Á
ÒѾÓÐ11È˻ظ´
ÉîÛÚ´óѧ˶ʿÕÐÉú£¨2026Ç´«¸ÐÆ÷·½Ïò£¬½ö¼ȡµÚÒ»Ö¾Ô¸£©
ÒѾÓÐ8È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú£¬Ð»Ð»£¡£¡£¡
ÒѾÓÐ3È˻ظ´
°ëÔÂ̸~2014
ÒѾÓÐ49È˻ظ´
¼±¼±¼±~~΢Æ×ÇóÖú£¬Ð»Ð»O(¡É_¡É)Oлл
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¡¸Ð¼¤£¡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл´ó¼Ò
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Íò·Ö¸Ðл~
ÒѾÓÐ5È˻ظ´
podÊý¾Ý´¦ÀíÇóÖú
ÒѾÓÐ12È˻ظ´
΢Æ×ÇóÖú£¬¶àлÁË
ÒѾÓÐ3È˻ظ´
ÇóÖú¦Á-¼×»ù±½ÒÒÏ©Óë¹ýÁ¿±½·ÓÔÚÁòËá¼ÓÈÈÌõ¼þÏ·¢Éúʲô·´Ó¦£¿
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¡¼±¼±¼±£¬Ð»Ð»£¡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬ÔÚÏßµÈ
ÒѾÓÐ4È˻ظ´
¼±Çó΢Æ×¿â²éѯ£¡·Ç³£¸Ðл£¡
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú ¼±¼±¼±£¡£¡£¡
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48805.6
- É¢½ð: 890
- ºì»¨: 208
- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
¿ÓµùÒ©»¯: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-04-14 15:54:53
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
¿ÓµùÒ©»¯: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-04-14 15:54:53
|
²éѯ½á¹û£º¹²²éµ½4¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . rhodomyrtone C26H34O6 ÏàËÆ¶È:80% Australian Journal of Chemistry 2002 55 229-232 Rhodomyrtone, an antibotic from Rhodomyrtus tomentosa Dachriyanus Salni, M. V. Sargent , B. W. Skelton, I. Soediro, M. Sutisna, A. H. White and E. Yulinah Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . rhodomyrtone C26H34O6 ÏàËÆ¶È:76.9% Tetrahedron 2013 69 8559-8563 Synthesis of the acylphloroglucinols rhodomyrtone and rhodomyrtosone B Marius Morkunas, Linda Dube, Friedrich Götz, Martin E. Maier Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 6,8-dihydroxy-9-isobutyl-2,2,4,4-tetramethyl-4,9-dihydro-1H-xanthene-1,3(2H)-dione C21H26O5 ÏàËÆ¶È:66.6% Tetrahedron 2013 69 8559-8563 Synthesis of the acylphloroglucinols rhodomyrtone and rhodomyrtosone B Marius Morkunas, Linda Dube, Friedrich Götz, Martin E. Maier Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . callistenone A C25H32O6 ÏàËÆ¶È:60% Tetrahedron 2013 69 6070-6075 Acylphloroglucinols from Callistemon lanceolatus DC. Suthida Rattanaburi, Wilawan Mahabusarakam, Souwalak Phongpaichit, Anthony R. Carroll Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2015-04-14 14:14:29













»Ø¸´´ËÂ¥