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thietane ring, with yields of 44 - 96%. The structures of these compounds were confirmed by IR and NMR

-butyl-3-methylxanthines in 85 – 98% yields. The structures of the compounds were confirmed by IR and PMR

steps by our improved method. The structures of the synthesized compounds were confirmed by IR and NMR

]- acetate salts containing thietanyl and dioxothietanyl rings. The structures of the synthesized compounds

]- acetate salts containing thietanyl and dioxothietanyl rings. The structures of the synthesized compounds

method for hypercoagulability/hypocoagulability, and the thrombosis model, using tissue factor (TF

. The structures of the synthesized compounds were confirmed by IR, PMR, and 13C and 15N NMR spectroscopy

. The structures of the synthesized compounds were confirmed by IR, PMR, and 13C NMR spectroscopy and GC-MS data

. The structures of the synthesized compounds were established by IR, PMR, and 13C NMR spectroscopy. In vitro

. The structures of the synthesized compounds were confirmed by IR, PMR, and 13C and 15N NMR spectroscopy

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