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C NMR chemical shift ranges R H. alkyl Y A11 substituents

C NMR chemical shift variation as a function of paramagnetic ion concentration.

C NMR chemical shift variations as a function of paramagnetic ion concentration versus

C NMR chemical shifts

C NMR chemical shifts for cations from cyclopentaphenanthrene derivatives .

C NMR chemical shifts for dications from cyclopentaphenanthrene derivatives .

C NMR chemical shifts for dications from cyclopentaphenanthrene derivatives in parentheses , f and t denote inter-

C NMR chemical shifts of substituted carbocations.

C NMR data for abyssinin.

C NMR data for artabotrine .

C NMR data for methyl- and 6-halo-chrysenium ions .

C NMR data for persistent carbocations from the benzanthracene derivatives and for related a-substituted carbocations and a-carboxonium ions .

C NMR data for podocarpane

C NMR data for pyrenium-carboxonium dications

C NMR data for pyrenyl-a-CF -substituted carbocations .

C NMR DEPT spectra of tinzaparin top and dalteparin bottom , 75 MHz, solvent D2O.

C NMR line position

C NMR nutation spectra of poly Sample prepared

C NMR obtained by lipase Novozym-435-catalyzed ring-opening polymerization in bulk at 60 C.

C NMR of biosynthetically C-enriched factor III octamethyl ester. The doub-let centre line intensities for C-20 and the C-20 methyl reflect a higher degree of enrichment from ALA than from methionine. Additional fine structure of the C-20 signal is due to long-range coupling with C-4

C NMR of ethyl glucoside acrylate

C NMR of MAGME monomer.

C NMR of the crude reaction mixture from the oxidation coupiing of methane to acetic acid-cataiyzed reaction

C NMR shifts for some 1,2,4-oxadiazoles. Source

C NMR solid state CP MAS spectra of compounds 1 at spinning speed lOkHz.



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