- Stereoelectronic effects on 1H nuclear magnetic resonance chemical shifts in methoxybenzenes
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(Graph Presented) Investigation of all O-methyl ethers of 1,2,3-benzenetriol and 4-methyl-1,2,3-benzenetriol (3-16) by 1H NMR spectroscopy and density-functional calculations disclosed practically useful conformational effects on 1H
- Lambert, Maja,Olsen, Lars,Jaroszewski, Jerzy W.
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p. 9449 - 9457
(2007/10/03)
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- Isolation and structural elucidation of biotransformation products from acarbose
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Following oral administration the α-glucosidase inhibitor acarbose (O-4,6-dideoxy-4-[[1S,4R,5S,6S)-4,5,6-trihydroxy-3-(hydroxymethyl)-2- cyclohexen-1-yl]amino]-α-D-glucopyranosyl-(1→4)-O-α-D-glucopyranosyl- (1→4)-D-glucopyranose, Bay g 5421) is degraded b
- Boberg,Kurz,Ploschke,Schmitt,Scholl,Schuller,Wunsche
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p. 555 - 563
(2007/10/02)
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