| ²é¿´: 332 | »Ø¸´: 1 | |||
¿ÓµùÒ©»¯Ìú³æ (³õÈëÎÄ̳)
|
[ÇóÖú]
΢Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë
|
|
CÆ×Êý¾Ý£º11.15,15.84,23.18,23.54,24.11,24.61,24.69,24.88,24.98, 25.03,28.30,45.43,46.34,47.22,56.09,100.31,105.13,105.95,114.38,152.81,159.61,164.15,167.41,198.56,209.28, 211.74 |
» ²ÂÄãϲ»¶
¸´ÊÔµ÷¼Á£¬Ò»Ö¾Ô¸Ö£ÖÝ´óѧ²ÄÁÏÓ뻯¹¤289·Ö
ÒѾÓÐ23È˻ظ´
»¯Ñ§¹¤³ÌÓë¼¼Êõרҵһ־Ը¹þ¹¤³Ì 291·ÖBÇø ¹ú¼Ò¼¶´ó´´¸ºÔðÈË ÓÐÒ»×÷ÂÛÎÄ
ÒѾÓÐ6È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ10È˻ظ´
314Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
µ÷¼Á »¯Ñ§ 307
ÒѾÓÐ8È˻ظ´
Ò»Ö¾Ô¸211 0703»¯Ñ§ 346·ÖÇóµ÷¼Á
ÒѾÓÐ11È˻ظ´
086003µ÷¼ÁÇóÖú
ÒѾÓÐ14È˻ظ´
085400 328·Ö Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
083200 ³õÊÔ305·Ö Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
284Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
yangyinhe
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1566 (½²Ê¦)
- ½ð±Ò: 15048.4
- ºì»¨: 21
- Ìû×Ó: 2773
- ÔÚÏß: 261.2Сʱ
- ³æºÅ: 942922
- ×¢²á: 2010-01-15
- ÐÔ±ð: MM
- רҵ: ÌìÈ»Óлú»¯Ñ§
¡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 2015-04-06 00:17:55
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
¿ÓµùÒ©»¯: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-04-06 00:17:55
|
1 . rhodomyrtosone B C26H34O6 ÏàËÆ¶È:80.7% 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 -------------------------------------------------------------------------------- 2 . Rhodomyrtosone B C26H34O6 ÏàËÆ¶È:76.9% Tetrahedron 2008 64 11193-11197 New acylphloroglucinols from the leaves of Rhodomyrtus tomentosa Asadhawut Hiranrat, Wilawan Mahabusarakam Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . rhodomyrtone C26H34O6 ÏàËÆ¶È:65.3% 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 -------------------------------------------------------------------------------- 4 . 1,3-Dioxo-4,9-dihydro-8-hydroxy-6-mthoxy-2,2,4,4-tetramethyl-5-(3-methyl-1-oxobutyl)-9-(2-mthyl-propyl)-1H-xanthene C27H36O6 ÏàËÆ¶È:62.9% Journal of Natural Products 1992 Vol 55 43 Antiviral Phloroglucinols from New Zealand Kunzea Species Stephen J. Bloor Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . Rhodomyrtosone A C26H32O7 ÏàËÆ¶È:61.5% Tetrahedron 2008 64 11193-11197 New acylphloroglucinols from the leaves of Rhodomyrtus tomentosa Asadhawut Hiranrat, Wilawan Mahabusarakam Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . rhodomyrtone C26H34O6 ÏàËÆ¶È:61.5% 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 |
2Â¥2015-04-03 18:11:13













»Ø¸´´ËÂ¥