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C-H transformation of a dihydronaphthalene.

C-H transformation of aldehydes

C-H transformation of imines

C-H transformation to 3,3-dihexylcyclopropene

C-H transformation to alkynylstannanes via formation of allenylstannanes.

C-H transformation to allenes

C-H transformation to methylenecyclopropanes

C-H transformation to vinyltins.

C-H transformations not requiring oxidants, with acid or salt formation.

C-H-O phase diagram for a mixture of 75 vol. hydrogen, 15 vol. carbon monoxide, the balance being carbon dioxide the boundary for carbon deposition is indicated by the straight line composition of water-free natural gas reformate ,

C-H-O phase diagram showing points regions of gas compositions suitable for diamond growth as well as non-diamond carbon growth region and no-growth region.

C-H-O phase diagram.

C-HandC-C activation in rhodium-pincer complexes

C-HSQC of PTPIB with ligand ligand. The chemical shift change for the isoleucine residue 219 indicates binding of the ligand to the corresponding amino acid

C-Hydroxymethyl-D-riburonic acid and its lactones. The open aldehyde form of the acid

C-I functionalization of 6-methylellipticine .

C-imidazolylsilver compounds.

C-induced surface stress on Ni-Uke structure, shown in

C-induced surface stress on Ni. The plateau in the stress curve starting at a coverage of 0.3 indicates the formation of the p4g reconstruction. Data from , rescaled to account for the one dimensional bending, coverage 1.0

C-INEPT spectrum

C-Isomaltose and

C-J pressure as a function of cylinder test wall velocity at 6 and 19 mm wall expansion.

C-J3 NMR spectrum at 25.2 MHz of a low-density PE produced from a high-pressure

C-K edge EELS of diamond, graphite and carbon onions with a diamond core , and amorphous carbon

C-l 3 A cycle whereby N2 is converted to useful organic products .



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