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×öÓÀÔ¶µÄ×Ô¼º: ½ð±Ò+8, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл£¡ 2015-04-08 00:11:06
1 .     Methyl (1R,2R,2'Z)-2-(5'-hydroxy-pent-2'-enyl)-3-oxocyclopentaneacetate
C13H18O4     ÏàËÆ¶È:92.3%
Bioscience, Biotechnology, and Biochemistry          2008          72          2867-2876
Synthesis and Bioactivity of Potassium ¦Â-D-Glucopyranosyl 12-Hydroxy Jasmonate and Related Compounds
Yoko NAKAMURA, Ryoji MIYATAKE, Sho INOMATA and Minoru UEDA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



2 .     Methyl (1R,2R,2'Z)-2-(5'-hydroxy-pent-2'-enyl)-3-oxocyclopentaneacetate
C13H18O4     ÏàËÆ¶È:92.3%
Bioscience, Biotechnology, and Biochemistry          2008          72          2867-2876
Synthesis and Bioactivity of Potassium ¦Â-D-Glucopyranosyl 12-Hydroxy Jasmonate and Related Compounds
Yoko NAKAMURA, Ryoji MIYATAKE, Sho INOMATA and Minoru UEDA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



3 .     (1S,2S,2'Z)-2-(5'-Hydroxy-pent-2'-enyl)-3-oxo-cyclopentaneacetic acid
C12H18O4     ÏàËÆ¶È:92.3%
Bioscience, Biotechnology, and Biochemistry          2008          72          2867-2876
Synthesis and Bioactivity of Potassium ¦Â-D-Glucopyranosyl 12-Hydroxy Jasmonate and Related Compounds
Yoko NAKAMURA, Ryoji MIYATAKE, Sho INOMATA and Minoru UEDA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



4 .     compound 4
     ÏàËÆ¶È:92.3%
Bioscience, Biotechnology, and Biochemistry          1996          60          732-735
Two Jasmonoid Glucosides and a Phenylvaleric Acid Glucoside from Perilla frutescens
Tomoyuki FUJITA, Kenji TERATO, Mitsuru NAKAYAMA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



5 .     (-)-Hydroxyjasmonic Acid
     ÏàËÆ¶È:84.6%
Journal of Agricultural and Food Chemistry          2000          48          235-238
Isolation and Structural Elucidation of Two New Glycosides from Sage (Salvia officinalis L.)
Mingfu Wang, Hiroe Kikuzaki, Nanqun Zhu, Sengming Sang, Nobuji Nakatani, and Chi-Tang Ho
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



6 .     12-ôÇ»ùÜÔÀòͪËá
C12H18O4     ÏàËÆ¶È:84.6%
Chinese Journal of Medicinal Chemistry          2012          22          38-43
Chemical constituents from the endophyte Bacillus pumilus derived from Breynia fruticosa
HUO Pei-yuan; CHEN Hua-hong; JIANG Yi; HAN Li; XU Li-hua; HUANG Xue-shi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



7 .     (1'R,5'R)-5-(5'-carboxymethyl-2'-oxocyclopentyl)-3Z-pentenyl acetate
C14H20O5     ÏàËÆ¶È:71.4%
Chemistry of Natural Compounds          2012          48          577-579
A new cyclopentanone derivative from Euphorbia hirta
Shao-Ming Chi, Yi Wang, Yan Zhao, Jian-Xin Pu and Xue Du, et al.
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



8 .     (1'S,4'R,6'R)-3'-Azabicyclo[4.4.0]decan-4'-essigsaure. a) Hydrochlorid
C11H20ClNO2     ÏàËÆ¶È:69.2%
Helvetica Chimica Acta          1980          63          1158-1175
Struktur eines O, N-Ketenacetals: (1 RS, 8 SR, 10 SR, 4(15)Z)-4-äthyliden-5-oxa-3-azatricyclo [8.4.0.03,8]tetradecan
Albin K¨¹min, Emily Maverick, Paul Seiler, Noel Vanier, Lorenz Damm, Reinhard Hobi, Jack D. Dunitz, Albert Eschenmoser
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



9 .     phenylalanine
     ÏàËÆ¶È:69.2%
Phytochemistry          1988          27          3417-3422
(l)-2,5-dihydrophenylalanine from the fireblight pathogen Erwinia amylovora
Gottfried J. Feistner
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



10 .     (+)-methyl dihydrojasmonate
C13H22O3     ÏàËÆ¶È:69.2%
Organic letters          2000          2          2959-2962
Enantioselective Synthesis of Both Enantiomers of Methyl Dihydrojasmonate Using Solid−Liquid Asymmetric Phase-Transfer Catalysis
Thierry Perrard, Jean-Christophe Plaquevent, Jean-Roger Desmurs, and Dominique H¨¦brault
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



11 .     compound 3b
     ÏàËÆ¶È:69.2%
Archiv der Pharmazie          1996          329          291-300
Asymmetric Synthesis and Structure-Activity Relationship of the Four Stereoisomers of the Antibiotic Amidinomycin Part 1: The Synthesis
Sun-Young Sung and August Wilhelm Frahm
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



12 .     3,3'-[(1R,2R)-cyclohexane-1,2-diamino]bis-{(1R,2R,5R)-2,6,6-trimethylbicyclo[3.1.1]heptan-2-ol}
C26H46N2O2     ÏàËÆ¶È:69.2%
Russian Journal of Organic Chemistry          2011          47          1130-1138
Synthesis of 1,2-diamine ligands based on natural monoterpenoids
I. A. Dvornikova, E. V. Buravlev, L. L. Frolova, Yu. V. Nelyubina and I. Yu. Chukicheva, et al.
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



13 .     methyl 5-(methylamino)-5-oxo-2-(2-oxo-2-phenylethyl)pentanoate
C15H19NO4     ÏàËÆ¶È:69.2%
European Journal of Organic Chemistry          2011                   4231-4240
Synthesis of Benzo[c]azocanones and Indeno[1,2-b]pyrroles from Oxoindanecarboxylates
Florian Behler, Florian Habecker, Wolfgang Saak, Thorsten Kl¨¹ner and Jens Christoffers
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



14 .     (3aS*,4R*,7S*,7aR*)-3-(4-chlorophenyl)-3a,4,5,6,7,7a-hexahydro-1H-4,7-methanoinden-1-one
C16H15ClO     ÏàËÆ¶È:69.2%
Molecules          2014          19          1763-1774
Pauson-Khand Reaction of Internal Dissymmetric Trifluoromethyl Alkynes. Influence of the Alkene on the Regioselectivity
Nuria Aiguabella, Elsa M. Arce, Carlos del Pozo, Xavier Verdaguer and Antoni Riera
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



15 .     Methyl (S)-1-[(1R)- or (1S)-cyclohex-2-en-1-yl]pyrrolidine-2-carboxylate
C12H19NO2     ÏàËÆ¶È:69.2%
Chirality          2014          26          793−800
Bromolactamization: Key Step in the Stereoselective Synthesis of Enantiomerically Pure, cis-Configured Perhydropyrroloquinoxalines
ADRIAN SCHULTE, XINGCI SITU, SUSUMU SAITO, AND BERNHARD WÜNSCH
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



16 .     Methyl (S)-1-[(1S)- or (1R)-cyclohex-2-en-1-yl]pyrrolidine-2-carboxylate
C12H19NO2     ÏàËÆ¶È:69.2%
Chirality          2014          26          793−800
Bromolactamization: Key Step in the Stereoselective Synthesis of Enantiomerically Pure, cis-Configured Perhydropyrroloquinoxalines
ADRIAN SCHULTE, XINGCI SITU, SUSUMU SAITO, AND BERNHARD WÜNSCH
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



17 .     Diethyl-3,3'-disulfanediylbis(2-(5-(1,2-dithiolane-3-yl)pentanamido))propanoate
C26H44N2O6S6     ÏàËÆ¶È:69.2%
Chemical Biology & Drug Design          2014          83          688−696
Synthesis of New Lipoic Acid Conjugates and Evaluation of Their Free Radical Scavenging and Neuroprotective Activities (pages 688¨C696)
Maria Laura Bolognesi, Christian Bergamini, Romana Fato, Joël Oiry, Jean-Jacques Vasseur and Michael Smietana
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



18 .     tert-butyl (S)-1-((S)-1-hydroxy-3-phenylpropan-2-ylamino)-4-methyl-1-oxopentan-2-ylcarbamate
C20H32N2O4     ÏàËÆ¶È:66.6%
Tetrahedron          2012          68          10114-10121
An efficient entry to highly substituted chiral 2-oxopiperazines from ¦Á-amino acids via iodocyclization
Amit Kumar Jana, Sanjit Kumar Das, Gautam Panda
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



19 .     12-OH-JA-Val
     ÏàËÆ¶È:66.6%
Phytochemistry          2014          99          6-13
CYP94B3 activity against jasmonic acid amino acid conjugates and the elucidation of 12-O-¦Â-glucopyranosyl-jasmonoyl-l-isoleucine as an additional metabolite
Naoki Kitaoka, Hiroshi Kawaide, Naruki Amano, Takuya Matsubara, Kensuke Nabeta, Kosaku Takahashi, Hideyuki Matsuura
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



20 .     (3aS*,4R*,7S*,7aR*)-3-(4-tolyl)-3a,4,5,6,7,7a-hexahydro-1H-4,7-methanoinden-1-one
C17H18O     ÏàËÆ¶È:66.6%
Molecules          2014          19          1763-1774
Pauson-Khand Reaction of Internal Dissymmetric Trifluoromethyl Alkynes. Influence of the Alkene on the Regioselectivity
Nuria Aiguabella, Elsa M. Arce, Carlos del Pozo, Xavier Verdaguer and Antoni Riera
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2015-04-07 05:38:21
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