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wushuai2255: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú, ´ó¸Å¿ò¼ÜÖªµÀÁË£¬Ð»Ð» 2012-07-31 22:43:26
1 .     5-(1,2-dihydroxyethyl)-3-hydroxy-4-(3-nitrooxypropoxy)-5H-furan-2-one
C9H13NO9     ÏàËÆ¶È:55.5%
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
2 .     5-(1,2-dihydroxyethyl)-4-hydroxy-3-(3-nitrooxypropoxy)-5H-furan-2-one
C9H13NO9     ÏàËÆ¶È:55.5%
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
3 .     dioscoran B
    ÏàËÆ¶È:50%
Planta Medica          1986          52          168-171
Isolation and Hypoglycemic Activity of Dioscorans A, B, C, D, E, and F; Glycans of Dioscorea japonica Rhizophors
Hiroshi Hikino , Chohaehi Konno, Michiko Takahashi, Miki Murakami, Yoshiaki Kato, Masami Karikura and Teruaki Hayashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     2,6-Dimethyl-4H-pyran-4-one-3,5-dicarboxylic acid,bis(2-methoxyethyl)ester
C15H20O8     ÏàËÆ¶È:50%
Molecules          2000          5          200-207
Chemistry of Pyrones, Part 3: New Podands of 4H-Pyran-4-ones
Aziz Shahrisa and Alireza Banaei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     direkt aus L-Ascorbinsaure
    ÏàËÆ¶È:50%
Helvetica Chimica Acta          1980          63          1728-1739
Synthese und Eigenschaften von 6-Desoxy-6-halogen-Derivaten der L-Ascorbins?ure
Joseph Kiss, Klaus Peter Berg, Adolf Dirscherl, Willi E. Oberh?nsli, Wolf Arnold
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     aquilegiolide
    ÏàËÆ¶È:50%
Fitoterapia          2001          72          706-708
7,8-Dihydrobenzofuranones from Ouratea reticulata
Salvador S. Elo Manga, Bernard B. Messanga ,Beibam L. Sondengam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     (3S,4R,5R)-tert-Butyl 3,4,5-trihydroxy-2-oxopiperidine-1-carboxylate
C10H17NO6     ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry          2011          19          41-51
Synthesis and in vitro anti-hepatitis B virus activity of six-membered azanucleoside analogues
Dan Wang, Yu-Huan Li, Yu-Ping Wang, Rong-Mei Gao, Li-He Zhang, Xin-Shan Ye
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     7-Ethoxy-N2-(2-methoxyethyl)thiazolo[4,5-d]pyrimidine-2,5-diamine
C10H15N5O2S     ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry          2011          19          702-714
Synthesis of novel 5-amino-thiazolo[4,5-d]pyrimidines as E. coli and S. aureus SecA inhibitors
Mi-Yeon Jang, Steven De Jonghe, Kenneth Segers, Jozef Ann¨¦, Piet Herdewijn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     2-amino-8-bromo-9-[(2-hydroxyethoxy)methyl]-1,9-dihydro-6H-purin-6-one
C8H10N5O3Br     ÏàËÆ¶È:50%
Heterocycles          2005          65          1967-1973
A Practical Synthesis of 8-Hydroxyacyclovir and 9-(Carboxymethoxymethyl)guanine, Metabolites of Acyclovir
Teruo Kutsuma, Yasuo Sakai, Hiroyuki Ouchi, Noriaki Shiina, Takehiro Yamagishi, Shiroshi Shibuya, and Tsutomu Yokomatsu*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     Compound (-)-7
    ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry Letters          2007          17          5974-5977
Arene cis-dihydrodiols: Useful precursors for the preparation of analogues of the anti-tumour agent, 2-crotonyloxymethyl-(4R,5R,6R)-4,5,6-trihydroxycyclohex-2-enone (COTC)
Claire L. Arthurs, James Raftery, Helen L. Whitby, Roger C. Whitehead, Natasha S. Wind, Ian J. Stratford
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     Compound 5-epi-4
    ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry Letters          1999          9          615-618
Homoisofagomines: Chemical-enzymatic synthesis and evaluation as ¦Á- and ¦Â-glucosidase inhibitors
Matthias Schuster
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     6¦Â-Hydroxy-2(6,7-dihydro-7¦Á¦ÂH)-benzofuranone
C8H8O3     ÏàËÆ¶È:50%
Phytochemistry          1984          23          2394-2396
A butenolide atypical of the Ranunculaceae: aquilegiolide from Aquilegia atrata (var. Atroviolacea)
Antonio Guerriero, Francesco Pietra
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     (+)-aquilegiolide
C8H8O2     ÏàËÆ¶È:50%
Chinese Journal of Natural Medicines          2006          4          260-263
Chemical Constituents of Securinega suffruticosa
WANG Ying; LI Qian; YE Wen-Cai; IP Fanny; IP Nancy; ZHAO Shou-Xun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     (3S,5S)-N-Acetyl-3-(N-methylcarbamoyl)-5-(hydroxymethyl)-isoxazolidine
C8H14N2O4     ÏàËÆ¶È:50%
Tetrahedron          2012          68          1762-1768
Cycloaddition of a chiral nitrone to allylic motifs: an access to enantiopure sugar-based amino acids displaying a stable glycosidic bond and to 4(S)-4-hydroxy-l-ornithine
Ka?ss Aouadi, Moncef Msaddek, Jean-Pierre Praly
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     (¡À)-(8R,8aR)-8-hydroxy-1,2,8,8a-tetrahydroindolizin-3(5H)-one
C8H11NO2     ÏàËÆ¶È:50%
Tetrahedron          2012          68          3692-3700
Application of the intramolecular PIFA-mediated amidation of alkynes to the synthesis of substituted indolizidinones Original Research Article
Leticia M. Pardo, Imanol Tellitu, Esther Dom¨ªnguez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     (¡À)-(8S,8aR)-8-hydroxy-1,2,8,8a-tetrahydroindolizin-3(5H)-one
C8H11NO2     ÏàËÆ¶È:50%
Tetrahedron          2012          68          3692-3700
Application of the intramolecular PIFA-mediated amidation of alkynes to the synthesis of substituted indolizidinones Original Research Article
Leticia M. Pardo, Imanol Tellitu, Esther Dom¨ªnguez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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