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tianming887

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tianming887: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-09-08 10:53:33
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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
2Â¥2013-09-08 09:39:13
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