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Macrographs of C C-SiC-ZrC composites before

Macrographs of fractured tensile samples having tensile axes perpendicular to the local long u y

Macrographs showing stirred zone in friction stir processed A356 using processing parameter combinations of . Source

Macroheterogeneity of catalyst 1 in the precursor state. The two left-hand figures show how two magnetite grains are separated by a crystal of calcium iron oxide . The right-hand figures demonstrate the uneven potassium distribution. The area A contains spherical particles of iron oxide.

Macroion-macroion radial distribution functions for System I using a spherical cutoff at Rcut 16Rm by employing the appropriate volume elements in the normalization. The thin solid line corresponds to a uniform distribution. Nm 80, L 32.224Rm, and

Macroion-macroion radial distribution functions for System IV with Nm 20

Macrol recorded.

Macrolactam synthesis by intramolecular reaction of an co-acyl chloride-amine

Macrolactone libraries.

Macrolactones prepared from the reductive cyclisation of ynals in the presence of NHC-nickel complexes

Macrolactones via allylic C—H oxidation by Pd catalysis .

Macrolactonisation reaction.

Macrolactonization and macrolactamization routes to FK228.

Macrolactonization of intermediate 34.

Macrolactonization protocols .

Macrolactonization reaction using polymeric carbodiimide 5.

Macrolactonization through RCM reaction and different reagents used for macrocyclization.

Macrolactonizations mediated by .

Macrolide antibiotics and other therapeutic amine drugs documented to inactivate certain P450 isoforms via MIcomplexation. Following cointake of these therapeutic amines with other therapeutic drugs, in vivo

Macrolide antibiotics originating from erythromycin A and their hydroxylated derivatives produced by P450

Macrolide binding interactions and

Macrolide conjugates of anti-inflammatoiy compounds. The compound code and its conjugated dmg are indicated below the structure.

Macrolide modifying enzymes. Macrolide antibiotics such as erythromycin .

Macrolide synthesis by free radical cyclization

Macrolidic antibiotics.



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