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Mechanism of the Formation of 2, 3, 5, 6-Tetrachlorophenylacetic Acid.
Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry
Organic Chemistry
(Z)-3-(9-Anthryl)-1-(4-Bromophenyl)-2-(4-Nitro-1h-Imidazol-1-Yl)prop-2-En-1-One
Acta Crystallographica Section E Structure Reports Online
Radical-Type Reactivity of the 1, 3-Dibora-2, 4-Diphosphoniocyclobutane-1, 3-Diyl
Interaction of the M4 Segment With Other Transmembrane Segments Is Required for Surface Expression of Mammalian Α-Amino-3-Hydroxy-5-Methyl-4-Isoxazolepropionic Acid (AMPA) Receptors
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Figure 6: Far-Uv CD Spectra of Wild Type (1), W674A (2), W707A (3), W737A (4) and W674a/W707a (5)CaD136.
2-[(E)-1-(4-Methoxyphenyl)pent-1-En-3-Ylidene]malononitrile
Acta Crystallographica Section E Structure Reports Online
Chemistry of 3-Carbonyl-2-Methyl-4-Oxo-4h-1-Benzopyrans
Arkivoc
Organic Chemistry
2-Benzyl-6-Chloro-1-(4-Methylphenyl)-1h-Indole-3-Carbonitrile
Acta Crystallographica Section E Structure Reports Online
1-[3-(2-Benzyloxy-6-Hydroxy-4-Methylphenyl)-5-[3,5-Bis(trifluoromethyl)phenyl]-4,5-Dihydro-1h-Pyrazol-1-Yl]propane-1-One
Acta Crystallographica Section E Structure Reports Online
3-(1,3-Benzodioxol-5-Yl)-1-Phenylprop-2-En-1-One
Acta Crystallographica Section E Structure Reports Online
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