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1 .     Methyl 2,6-dideoxy-3-O-methanesulfonyl-6-C-methyl-¦Á-D-arabino-hexopyranoside
    ÏàËÆ¶È:55.5%
Canadian Journal of Chemistry          2005          83          801-811
Design and synthesis of oxazolidinone ketolide antibiotic segment mimetics1
Stephen Hanessian and Kiran Kumar Kothakonda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     compound 13
C35H41ClF6NO2P2Rh     ÏàËÆ¶È:55.5%
Zeitschrift f¨¹r Naturforschung B          2010          65          679-686
Metal Complexes of Biologically Important Ligands, CLXXV. Pentamethylcyclopentadienyl Halfsandwich Complexes of Rhodium(III) and Iridium(III) with Schiff Bases from 2-(Diphenylphosphino)benzaldehyde and a-Amino Acid Esters
B. Schreiner, B. Wagner-Schuh, and W. Beck
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     (4RS,5RS)-4-amino-1,5-di(propan-2-yl)pyrazolidin-3-one
C9H19N3O     ÏàËÆ¶È:55.5%
Helvetica Chimica Acta          2014          97          245-267
A Simple Synthesis of Polyfunctionalized 4-Aminopyrazolidin-3-ones as ¡®Aza-deoxa¡¯ Analogs of D-Cycloserine
Ana Novak, Matej Štefanič, Uroš Grošelj, Martina Hrast, Marta Kasunič, Stanislav Gobec, Branko Stanovnik and Jurij Svete
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     compound 6
C12H16O3     ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          1994          42          736-738
ABSOLUTE STEREOSTRUCTURES OF PAEONISOTHUJONE, A NOVEL SKELETAL MONOTERPENE KETONE, AND DEOXYPAEONISUFFRONE, AND ISOPAEONISUFFRAL, TWO NEW MONOTERPENES, FROM MOUTAN CORTEX
Masayuki YOSHIKAWA,Emiko HARADA,Toshie MINEMATSU,Osamu MURAOKA,Johji YAMAHARA,Nobutoshi MURAKAMI and Isao KITAGAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     compound 4b
C10H20O3     ÏàËÆ¶È:50%
Helvetica Chimica Acta          1981          64          761-768
Notiz ¨¹ber die Bestimmung der absoluten Konfiguration von (+)-2-Hydroxy-2, 3-dimethylbuttersäure
Hansj¨¹rg Wetter
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     (-)-5-exo-hydroxyborneo
C10H18O2     ÏàËÆ¶È:50%
Journal of Natural Products          1988          Vol 51          142
(-)- 5-exo-Hydroxyborneol : Isolation and Nmr Spectral Assignments
Y. A. G. P. Gunawardana, Geoffrey A. Cordell, I. Ralph C. Bick
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     fenchanediol
    ÏàËÆ¶È:50%
Phytochemistry          1991          30          3981-3987
Biotransformation of monoterpenoids, (−- and menthols, terpinolene and carvotanacetone by Aspergillus species
Yoshinori Asakawa, Hironobu Takahashi, Masao Toyota, Yoshiaki Noma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     compound 7f
    ÏàËÆ¶È:50%
Tetrahedron Letters          2003          44          5811-5814
A facile synthesis of 1,2-oxaphospholenes and stereoselective conversion into oxaphospholanes
Jung Hwan Hah, Bum Sung Lee, Shi Yong Lee, Hee-Yoon Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     compound 5c
C10H20N4     ÏàËÆ¶È:50%
Tetrahedron Letters          2004          45          6129-6132
Regiospecific solid-phase synthesis of substituted 1,2,3-triazoles
Makam S Raghavendra, Yulin Lam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     2,3-dihydro-1¦Á,3¦Á-dihydroxy-terpinolene
C10H18O2     ÏàËÆ¶È:50%
Zeitschrift f¨¹r Naturforschung C          2002          57          863-866
Detoxification of Terpinolene by Plant Pathogenic Fungus Botrytis cinerea
A. Farooq, M. I. Choudhary, Atta-ur-Rahman, S. Tahara, K. H. C. Ba\cser, and F. Demirci
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     (-)-isothujol
    ÏàËÆ¶È:50%
Organic Magnetic Resonance          1974          6          184-189
The NMR spectra and conformations of cyclic compounds: IX¡ªconformational studies of bicyclo(3,1,0)hexane derivatives by 13C NMR
Raymond J. Abraham, Collette M. Holden, Philip Loftus and David Whittaker
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     Isothujylalkohol
    ÏàËÆ¶È:50%
Organic Magnetic Resonance          1975          7          426-432
13C-NMR-Spektren von Monoterpenen
F. Bohlmann, R. Zeisberg and E. Klein
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     Methyl 3-O-[(R)-1-(Methoxycarbony1)ethyl]-¦Á-L-rhamnopyranoside
C11H20O7     ÏàËÆ¶È:50%
Journal of the American Chemical Society          1993          115          1114-1120
A novel approach for stereochemical analysis of 1-carboxyethyl sugar ethers by NMR spectroscopy
Wayne B. Severn, James C. Richards
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     (2R,4S,5R)-2,4,6-Trimethylheptane-1,5-diol
C10H22O2     ÏàËÆ¶È:50%
The Journal of Organic Chemistry          1993          58          2923-2926
A sex pheromone isolated from Macrocentrus grandii: absolute stereochemistry determination and implications
Injae Shin, Hui Qiang Zhou, Nanette Loida S. Que, Hung Wen Liu, Paul D. Swedenborg, Richard L. Jones
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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