|
|
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1 yutong307(¶¹¸ç´ú·¢): ½ð±Ò+30, лл 2013-12-07 15:42:41
²éѯ½á¹û£º¹²²éµ½15¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
--------------------------------------------------------------------------------
1 . dihydrophaseic acid
ÏàËÆ¶È:66.6%
Chemistry of Natural Compounds 2009 45 545-546
COMPONENTS OF Sophora alopecuroides SEEDS
Guan Ye, Chun-Hui Ma, Xiang-Yuan Huang,Zhi-Xiong Li, and Cheng-Gang Huang
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
2 . dihydrophaseic acid
ÏàËÆ¶È:66.6%
Chinese Traditional and Herbal Drugs 2009 40 847-849
Chemical constituents in green walnut husks of Juglans regia
ZHANG Jian-bin; LIU Jun-xi; ZHA Fei; DI Duo-long
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
3 . compound 11b
C12H20O2 ÏàËÆ¶È:58.3%
Tetrahedron Letters 2001 42 8489-8491
Asymmetric synthesis of tricyclic-cyclobutane by means of enantioselective deprotonation and intramolecular Michael¨Caldol reaction
Kiyosei Takasu, Keiko Misawa, Masataka Ihara
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
4 . p-Tolyl 3-amino-3-N,4-O-carbonyl-2,3,6-trideoxy-1-thio-¦Á-L-lyxo-hexopyranoside
C14H17NO3S ÏàËÆ¶È:58.3%
Acta Crystallographica Section E 2006 62 o2788-o2790
p-Tolyl 3-amino-3-N,4-O-carbonyl-2,3,6-tride­oxy-1-thio-¦Á-l-lyxo-hexopyran­oside
Guizhong Qi, Matthew T. Mendlik, Robert S. Coleman, Todd L. Lowary and Michael J. Ferguson
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
5 . platycodigenin
ÏàËÆ¶È:54.5%
Chemical & Pharmaceutical Bulletin 1978 26 671-673
Structures of Prosapogenins from Roots of Platycodon grandiflorum determined by Carbon-13 and Hydrogen-1 Nuclear Magnetic Resonance Spectroscopy
HIROSHI ISHII,KAZUO TORI,TAKEHIKO TOZYO and YOHKO YOSHIMURA
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
6 . 6-endo-hydroxycamphor
C10H16O2 ÏàËÆ¶È:54.5%
Phytochemistry 1997 45 755-763
Sesquiterpene lactones from Artemisia lucentica
J. Alberto Marco, Juan F. Sanz-Cervera, Vicente Garc¨ªa-Lliso, Natalia Batlle
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
7 . compound 4
C10H12O3 ÏàËÆ¶È:54.5%
Tetrahedron Letters 2005 46 7407-7410
Synthetic studies toward merrilactone A: a short synthesis of AB ring motif
Kenichi Harada, Hiroaki Kato, Yoshiyasu Fukuyama
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
8 . [(2-endo,3-exo)-3-methyl-bicyclo{2.2.1}hept-5-ene-2-carbonyl]-phosphonic acid diethyl ester
ÏàËÆ¶È:54.5%
Tetrahedron 2002 58 6521-6529
Lewis acid promoted cyclocondensations of ¦Á-ketophosphonoenoates with dienes¡ªfrom Diels¨CAlder to hetero Diels¨CAlder reactions
Stephen Hanessian, Philippe Compain
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
9 . 3-exo-methyl-7-iospropylidenenorborn-5-en-2-one
C11H14O ÏàËÆ¶È:54.5%
Canadian Journal of Chemistry 1987 65 789-797
13C magnetic resonance studies. 129. Homoenolization in the camphenilone system. Examination of some 7-substituted derivatives
Sriyawathie Peiris, Arthur J. Ragauskas, J. B. Stothers
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
10 . 3¦Â-Hydroxyapotrichothecene
C15H24O3 ÏàËÆ¶È:54.5%
The Journal of Organic Chemistry 1989 54 4313-4318
New mycotoxins from Fusarium sambucinum
Dale R. Sanson, David G. Corley, Charles L. Barnes, Scott Searles, Elmer O. Schlemper, Michael S. Tempesta, George E. Rottinghaus
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
11 . monoacetate
C12H16O5 ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin 2000 48(9) 1327-1331
Bioactive Constituents of Chinese Natural Medicines. V. Radical Scavenging Effect of Moutan Cortex. (1) : Absolute Stereostructures of Two Monoterpenes, Paeonisuffrone and Paeonisuffral
Masayuki YOSHIKAWA,Toshio OHTA,Atsuhiro KAWAGUCHI and Hisashi MATSUDA
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
12 . paeonisuffrone monoacetate
C12H16O5 ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin 1993 41 630-632
ABSOLUTE STEREOSTRUCTURES OF PAEONISUFFRONE AND PAEONISUFFRAL, TWO NEW LABILE MONOTERPENES, FROM CHINESE MOUTAN CORTEX
Masayuki YOSHIKAWA,Emiko HARADA,Atsuhiro KAWAGUCHI,Johji YAMAHARA,Nobutoshi MURAKAMI and Isao KITAGAWA
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
13 . 6,6-(ethylenedioxy)-4,5,5-trimethyl-8-methylenebicyclo[2.2.2]octan-2-one
C14H20O3 ÏàËÆ¶È:50%
Indian Journal of Chemistry Section B 2005 44B 751-761
Approaches to sesquiterpenes containing three contiguous quaternary carbon atoms. Synthesis of 3-methoxythapsene
Srikrishna,A; Ramachary,D B
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
14 . compound 15
ÏàËÆ¶È:50%
Tetrahedron Letters 2002 43 2765-2768
Stereospecific construction of three contiguous quaternary carbon atoms. Synthesis of (¡À)-3-methoxythaps-8-ene
A. Srikrishna, D.B. Ramachary
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
15 . (1R,2R,3R,6S)-3-methoxy-6-(1-methoxy-1-methylethyl)-3-methylcyclohexane-1,2-diol
ÏàËÆ¶È:50%
Russian Journal of Organic Chemistry 2003 39 985-991
Acid-Catalyzed Reactions of 2,3-Epoxy Derivatives of Citral with Alcohols
O. I. Yarovaya, D. V. Korchagina, O. V. Salomatina, M. P. Polovinka and V. A. Barkhash
Structure 13C NMR ̼Æ×Ä£Äâͼ
-------------------------------------------------------------------------------- |
|