| ²é¿´: 216 | »Ø¸´: 1 | ||
libinoookľ³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
ÇóÖú΢Æ×Êý¾Ý8
|
| 13C NMR (101 MHz, dmso) ¦Ä8.67,31.37,56.50,106.02,127.13,141.20,147.86,199.06, |
» ²ÂÄãϲ»¶
²ÄÁϵ÷¼Á
ÒѾÓÐ4È˻ظ´
304Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ24È˻ظ´
Ò»Ö¾Ô¸»ª¶«Àí¹¤085601²ÄÁϹ¤³Ì303·ÖÇóµ÷¼Á
ÒѾÓÐ7È˻ظ´
288»·¾³×¨Ë¶,Çóµ÷²ÄÁÏ·½Ïò
ÒѾÓÐ25È˻ظ´
0703»¯Ñ§
ÒѾÓÐ25È˻ظ´
Çóµ÷¼Á Ò»Ö¾Ô¸Î÷ÄϽ»Í¨´óѧ085701»·¾³¹¤³Ì 282·Ö
ÒѾÓÐ12È˻ظ´
Ò»Ö¾Ô¸211£¬»¯Ñ§Ñ§Ë¶£¬310·Ö£¬±¾¿ÆÖصãË«·Ç£¬Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Ò»Ö¾Ô¸211£¬0703»¯Ñ§305·ÖÇóµ÷¼Á
ÒѾÓÐ12È˻ظ´
Ò»Ö¾Ô¸211£¬»¯Ñ§Ñ§Ë¶£¬310·Ö£¬±¾¿ÆÖصãË«·Ç£¬Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
»¯ºÏÎï΢Æ×ÇóÖú лл
ÒѾÓÐ9È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý YC-8
ÒѾÓÐ7È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
΢Æ×Êý¾Ý²éѯÇóÖú
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý
ÒѾÓÐ3È˻ظ´
¹òÇóÄÜÓÃ΢Æ×Êý¾Ý¿âµÄ³æ×ÓÃÇ£¬°ïæ²éÒ»ÏÂ̼Æ×Êý¾Ý£¬±¾ÈËËÍ6¸ö½ð±Ò£¡£¡£¡
ÒѾÓÐ7È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
¡¾ÇóÖú¡¿ÇóGaussView5.0.8µÄʹÓÃÊֲᣡ£¡£¡£¡£¡£¡£¡£¡£¡
ÒѾÓÐ5È˻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
libinoook: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-09-29 08:02:21
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
libinoook: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-09-29 08:02:21
|
²éѯ½á¹û£º¹²²éµ½93¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . 3,5-¶þ¼×Ñõ»ù-4-ôÇ»ù-±½±ûͪ ÏàËÆ¶È:100% Lishizhen Medicine and Materia Medica Research 2012 23 3006-3007 Isolation and Identification of Flavonoids and Phenolic Constituents from Selaginella uncinata(Desv.) Spring ZHENG Jun-xia; ZHENG Yang; ZHANG Lei; ZHAO Su-qing; FANG Yan-xiong; ZHANG Kun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 3,5-dimethoxy-4-hydroxypropiophenone ÏàËÆ¶È:87.5% Chinese Pharmaceutical Journal 2005 40 255-258 Study on phenolic constituents of Pholidota yunnanensis BI Zhi ming, WANG Zheng tao *, XU Luo shan, XU Guo jun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 1-(4-hydroxy-3,5-dimethoxyphenyl)propan-1-one ÏàËÆ¶È:87.5% Natural Product Research and Development 2008 20 5-7 Chemical Components of Arundina graminifolia ZHU Hui;SONG Qi-shi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 1-(3',4',5'-Trimethoxyphenyl)propan-1-one C12H16O4 ÏàËÆ¶È:66.6% Canadian Journal of Chemistry 2005 83 1826-1832 Microwave- and ultrasound-assisted semisynthesis of natural methoxylated propiophenones from isomeric mixture of phenylpropenes in minutes1 Bhupendra P. Joshi, Anuj Sharma, and Arun K. Sinha Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 3,4,5-trimethoxypropiophenone ÏàËÆ¶È:62.5% Phytochemistry 1996 43 1089-1092 Lignans, ¦Ã-lactones and propiophenones of Virola surinamensis Norberto Peporine Lopes, Ema Ester de Almeida Blumenthal, Alberto Jos¨¦ Cavalheiro, Massuo Jorge Kato, Massayoshi Yoshida Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . sinapaldehyde ÏàËÆ¶È:62.5% China Journal of Chinese Materia Medica 2010 35 3161-3164 Chemical constituents of Swertia macrosperma WANG Hongling; GENG Chang¡äan; ZHANG Xuemei; MA Yunbao; JIANG Zhiyong; CHEN Jijun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . sinapaldehyde ÏàËÆ¶È:62.5% China Journal of Chinese Materia Medica 2011 36 1454-1457 Chemical constituents of Halenia elliptica WANG, Hongling, CHEN, Hao, GENG, Chang'an, ZHANG, Xuemei Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 3-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-1-propanone ÏàËÆ¶È:62.5% China Journal of Chinese Materia Medica 2011 36 2212-2214 Isoprenoids and Phenylpropanoids from Saussurea deltoidea HUANG, Huoqiang, YAN, Meina, PIAO, Xianglan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . compound 8 ÏàËÆ¶È:55.5% Chemical & Pharmaceutical Bulletin 1984 32 2622-2627 O-Methylation Effect on the Carbon-13 Nuclear Magnetic Resonance Signals of ortho-Disubstituted Phenols and Its Application to Structure Determination of New Phthalides from Aspergillus silvaticus MASAO FUJITA,MIKIKO YAMADA,SHOICHI NAKAJIMA,KENICHI KAWAI and MASAHIRO NAGAI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . methyl sinapate C12H14O5 ÏàËÆ¶È:55.5% Korean Journal of Pharmacognosy 2000 31(4) 434-437 Isolation of Sinapic Acid Esters from Raphani Semen Kang, Eun-Jung; Ko, Byoung-Seob; Kim, Ho-Kyoung Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-09-29 07:52:20














»Ø¸´´ËÂ¥