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²éѯ½á¹û£º¹²²éµ½14¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ 7 . fenchanediol ÏàËÆ¶È:50% Phytochemistry 1991 30 3981-3987 Biotransformation of monoterpenoids, (− - and menthols, terpinolene and carvotanacetone by Aspergillus speciesYoshinori Asakawa, Hironobu Takahashi, Masao Toyota, Yoshiaki Noma Structure 13C NMR ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |

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- and menthols, terpinolene and carvotanacetone by Aspergillus species