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zchangll

гæ (ÕýʽдÊÖ)


[ÇóÖú] ΢Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë

26-28-4
DMSO 13C NMR
7.3,11.7,21.5.37.8,42.5,48.6,60.1,61.9,162.1,162.4
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zchangll: ½ð±Ò+8, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-04-24 16:06:44
1 .     6-endo-hydroxycamphor
C10H16O2     ÏàËÆ¶È:50%
Phytochemistry          1997          45          755-763
Sesquiterpene lactones from Artemisia lucentica
J. Alberto Marco, Juan F. Sanz-Cervera, Vicente Garc¨ªa-Lliso, Natalia Batlle
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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2 .     ethyl 2-N-propylamino-1,3-thiazole-5-carboxylate
C9H14N2O2S     ÏàËÆ¶È:50%
Journal of Heterocyclic Chemistry          2003          40          353-356
Synthesis of novel 2-amino-1,3-thiazole-5-carboxylates utilising ultrasonic and thermally mediated aminolysis
Luke A. Baker and Craig M. Williams
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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3 .     Compound 6
    ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry Letters          2001          11          1679-1681
Ethambutol analogues as potential antimycobacterial agents
Herwig Häusler, R. Pamela Kawakami, Eva Mlaker, Wayne B. Severn, Arnold E. St¨¹tz
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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4 .     compound 3b
    ÏàËÆ¶È:50%
Tetrahedron Letters          2003          44          587-589
A novel approach to bicyclic fused cyclopentenone derivatives
Guisheng Deng, Xue Tian, Jianbo Wang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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5 .     des-A,B-8¦Â-[(triethylsilyl)oxy]-testosterone
C16H32O2Si     ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry          2009          17          7658-7669
Removal of the 20-methyl group from 2-methylene-19-nor-(20S)-1¦Á,25-dihydroxyvitamin D3 (2MD) selectively eliminates bone calcium mobilization activity
Rafal Barycki, Rafal R. Sicinski, Lori A. Plum, Pawel Grzywacz, Margaret Clagett-Dame, Hector F. DeLuca
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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6 .     endo-6'-bicyclo[3.1.1]heptylsyn-7-bromo-endo-6-bicyclo-[3.1.1]heptyl sulfone
C14H21BrO2S     ÏàËÆ¶È:50%
Russian Journal of Organic Chemistry          2002          38          1582-1587
Products of Reaction of Tricyclo[4.1.0.02,7]heptane and 1-Bromotricyclo[4.1.0.02,7]heptane with Hydrogen Sulfide, and Syntheses Based Thereon
V. A. Vasin, S. G. Kostryukov and V. V. Razin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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7 .     (1-chloro-2-p-tolylthioethyl)oxirane
C11H13ClOS     ÏàËÆ¶È:50%
Russian Journal of Organic Chemistry          2001          37          339-344
Reactions of Dichlorocarbene and Arenesulfenyl Chlorides with 3,4-Epoxy-1-butene and Vinylethylene Carbonate
T. G. Mannafov, E. A. Berdnikov and Ya. D. Samuilov
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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8 .     (R)-[2-(4-methylbenzyl)oxiran-2-yl]methanol
C11H14O2     ÏàËÆ¶È:50%
European Journal of Organic Chemistry          2010                   6840-6849
Chiral Primary Amine Catalyzed Asymmetric Epoxidation of ¦Á-Substituted Acroleins
Jiuyuan Li, Niankai Fu, Long Zhang, Pengxin Zhou, Sanzhong Luo and Jin-Pei Cheng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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9 .     compound 51
C17H36O3Si     ÏàËÆ¶È:50%
Tetrahedron          2013          69          7746-7758
Stereoselectivity of electrophile-promoted oxacyclizations of 1,4-dihydroxy-5-alkenes to 3-hydroxytetrahydropyrans
Frank E. McDonald, Kento Ishida, Jessica A. Hurtak
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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10 .     (7S,8R,9S,10R)-rel-1H,4H-8,9-bis[(acetyloxy)methyl]-3a,6a-butano-7,10-methano imidazo[4,5-d]imidazole-2,5(3H,6H)dione
C15H20N4O6     ÏàËÆ¶È:50%
Tetrahedron          2013          69          9957-9965
Bi(OTf)3¡ªa mild catalyst for the synthesis of difficult to obtain C-alkyl substituted glycolurils
Feng Wu, Vijaybabu Mandadapu, Anthony I. Day
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2015-02-05 11:09:53
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