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tianming887: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-09-08 10:53:33
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tianming887: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-09-08 10:53:33
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²éѯ½á¹û£º¹²²éµ½426¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound 11 ÏàËÆ¶È:63.6% Lipids 2005 40 833-838 Isolation and characterization of some hydroxy fatty and phosphoric acid esters of 10-hydroxy-2-decenoic acid from the royal jelly of honeybees (Apis mellifera) Naoki Noda, Kazue Umebayashi, Takafumi Nakatani, Kazumoto Miyahara and Kaori Ishiyama Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 12 ÏàËÆ¶È:63.6% Lipids 2005 40 833-838 Isolation and characterization of some hydroxy fatty and phosphoric acid esters of 10-hydroxy-2-decenoic acid from the royal jelly of honeybees (Apis mellifera) Naoki Noda, Kazue Umebayashi, Takafumi Nakatani, Kazumoto Miyahara and Kaori Ishiyama Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (5R,6R)-6-hydroxymethyl-3,3-dimethyl-5-(4-bromophenyl)tetrahydropyrazolo[1,2-a]pyrazol-1-one C15H18BrN2O2 ÏàËÆ¶È:61.5% Heterocycles 2010 81 1669-1688 Asymmetric 1,3-Dipolar Cycloaddition Reactions of Azomethine Imines with Acrolein Catalyzed by L-Proline and Its Derivatives Hiroyuki Suga, Tadashi Arikawa, Kennosuke Itoh, Yukihisa Okumura, Akikazu Kakehi, and Motoo Shiro Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . lucknolide A C10H12O6 ÏàËÆ¶È:60% Organic Letters 2010 Vol.12,No.17 3800-3803 Lucknolides A and B, Tricyclic Ketal-lactone Metabolites from a Terrestrial Streptomyces sp Prem P. Yadav, Vimal Nair, Birger Dittrich, Anja Sch¨¹ffler, and Hartmut Laatsch Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (E)-Deca-2-en-6,8-diyn-1-ol C10H12O ÏàËÆ¶È:60% The Journal of Organic Chemistry 2011 76 4467-4481 Polyunsaturated Alkyl Amides from Echinacea: Synthesis of Diynes,Enynes, and Dienes Nicholas J. Matovic, Patricia Y. Hayes, Kerry Penman, Reginald P. Lehmann,and James J. De Voss Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 7-(2-acetoxyethoxymethyl)-2-aminopurin-6-thione C10H13N5O3S ÏàËÆ¶È:60% Heterocycles 2005 65 787-796 Synthesis and Comparative Cytostatic Activity of the New N-7 Acyclic Purine Nucleoside Analogues with Natural N-9 Regioisomers Svjetlana Prekupec, Blanka Kalokira, Mira Grdisa, Kresimir Pavelic, Erik De Clercq, Mladen Mintas, and Silvana Raic-Malic* Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 3-O-Allyl-2-O-methyI-L-ascorbic acid ÏàËÆ¶È:60% Archives of Pharmacal Research 2005 28 377-381 Synthesis of polymeric thiazolidinediones and L-ascorbic acid towards the development of insulin-sensitizer Sun Mi Lee and Raok Jeon Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 9b C10H14N2O ÏàËÆ¶È:60% Tetrahedron Letters 2001 42 6451-6454 Synthesis and conformational properties of N-monoalkyl 1,5-diaza-cis-decalins Xu Xie, Dana A Freed, Marisa C Kozlowski Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 3a C11H16NO6P ÏàËÆ¶È:60% Tetrahedron Letters 2002 43 8711-8712 Reactions of diethyl mesyl- or tosyloxyphosphonates with diethyl phosphite and base: a method claimed to yield bisphosphonates Erik Årstad, Lars Skattebøl Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 10 C10H18O4 ÏàËÆ¶È:60% Tetrahedron Letters 2004 45 1763-1767 Unprecedented chemo-enzymatic synthesis of stereochemically pure 3-acetoxy-2-methyl-2-vinylcycloalkanones Ken-ichi Fuhshuku, Mina Tomita, Takeshi Sugai Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 1-methyl-3-(4-phenylpiperazin-1-yl)-pyrolidin-2-one C15H21N3O ÏàËÆ¶È:60% Tetrahedron Letters 2005 46 153-156 A novel and unusual method for C-N bond formation in 1-substituted-pyrrolidin-2-ones Neelima Sinha, Sanjay Jain, Nitya Anand Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 6-Bromo-2-(morpholin-4-yl)benzothiazole C11H11BrN2OS ÏàËÆ¶È:60% Heterocycles 2011 83 2589-2596 One-Pot Synthesis of Benzothiazol-2-amines by Cyclization of the Adducts between 2-Iodophenyl Isothiocyanates and Amines under Metal-Free Conditions Kazuhiro Kobayashi,* Akihiro Kobayashi, Kazuya Murahashi, and Shuhei Fukamachi Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 4-tert-butyl-2,7-hydro-1H-oxepin C10H16O ÏàËÆ¶È:60% Heterocycles 2000 53 897-904 Easy Access to Medium Rings by Entropy/Strain Reduction, Part 4. A Simple and Mild Route to Some Substituted 2,7-Dihydro-1H -oxepins, thiepins and a Phosphepin James G. Walsh and Declan G. Gilheany* Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . (S,Z)-4-ethylidene-2-(hydroxymethyl)pyrrolidine C7H13NO ÏàËÆ¶È:60% The Journal of Organic Chemistry 2010 75 8508-8515 Isolation, Structural Assignment, and Total Synthesis of Barmumycin Adriana Lorente, Daniel Pla, Librada M. Canedo, Fernando Albericio, and Mercedes Alvarez Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 4-[2-(1,2-dihydroxyethyl)-4-hydroxy-5-oxo-2,5-dihydrofuran-3-yloxymethyl]-furoxan-3-carboxylic acid amide C10H11N3O9 ÏàËÆ¶È:60% Bioorganic & Medicinal Chemistry 2008 16 5199-5206 Novel antioxidant agents deriving from molecular combination of Vitamin C and NO-donor moieties Clara Cena, Konstantin Chegaev, Silvia Balbo, Loretta Lazzarato, Barbara Rolando, Marta Giorgis, Elisabetta Marini, Roberta Fruttero, Alberto Gasco Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . compound IIc ÏàËÆ¶È:60% Russian Journal of Organic Chemistry 2009 45 365-373 Pincer ligands based on ¦Á-amino acids: III. New ligands based on 4-substituted phenols and their copper complexes. Enantioselective recognition of tyrosine N. E. Borisova, V. A. Knizhnikov, T. G. Gulevich, M. Yu. Seliverstov and E. A. Borisov, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . N,N'-(2-hydroxy-5-methylbenzene-1,3-diyldimethylidene)bis[(2S)-2-amino-3-hydroxypropanoic acid] C15H18N2O7 ÏàËÆ¶È:60% Russian Journal of Organic Chemistry 2009 45 365-373 Pincer ligands based on ¦Á-amino acids: III. New ligands based on 4-substituted phenols and their copper complexes. Enantioselective recognition of tyrosine N. E. Borisova, V. A. Knizhnikov, T. G. Gulevich, M. Yu. Seliverstov and E. A. Borisov, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . compound 8 ÏàËÆ¶È:60% Lipids 2005 40 833-838 Isolation and characterization of some hydroxy fatty and phosphoric acid esters of 10-hydroxy-2-decenoic acid from the royal jelly of honeybees (Apis mellifera) Naoki Noda, Kazue Umebayashi, Takafumi Nakatani, Kazumoto Miyahara and Kaori Ishiyama Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . N,N-bis(2-hydroxyethyl)-N-methyl-N-(2-nitrobenzyl)ammonium chloride C12H19ClN2O4 ÏàËÆ¶È:60% Journal of Medicinal Chemistry 1996 39 1084-1094 Hypoxia-Selective Antitumor Agents. 12. Nitrobenzyl Quaternary Salts as Bioreductive Prodrugs of the Alkylating Agent Mechlorethamine Moana Tercel, William R. Wilson, Robert F. Anderson, and William A. Denny Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . N,N-bis(2-chloroethyl)-N-methyl-N-(2-nitrobenzyl)ammonium chloride C12H17Cl3N2O2 ÏàËÆ¶È:60% Journal of Medicinal Chemistry 1996 39 1084-1094 Hypoxia-Selective Antitumor Agents. 12. Nitrobenzyl Quaternary Salts as Bioreductive Prodrugs of the Alkylating Agent Mechlorethamine Moana Tercel, William R. Wilson, Robert F. Anderson, and William A. Denny Structure 13C NMR ̼Æ×Ä£Äâͼ |
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