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Transformation of a phenol into a chloroaromatic compound by Ar-SN reaction via a Meisenheimer complex.

Transformation of a polynuclear aromatic hydrocarbon to carbon

Transformation of a racemic compound into a conglomerate.

Transformation of a reactive protein side chain to a lysinoalanine side chain via elimination and crosslink formation. Note that the intermediate carbanion has lost the original asymmetry. The carbanion can combine with a proton to regenerate the original amino acid which is then racemic, or undergo an elimination reaction to form dehydroalanine.

Transformation of a real non-symmetric matrix, X

Transformation of a real symmetric matrix, X CTBC

Transformation of a rectangle into o torus.

Transformation of a rectangular C lattice into a primitive P lattice

Transformation of a seed oil based feedstock, methyl oleate, using catalytic olefin metathesis

Transformation of a slow center into a fast one

Transformation of a tetragonal crystal, with lattice parameters aT bT, into a multiply twinned orthorhombic crystal with lattice parameters a0, bQ. The twinned regions are often called domains and the boundaries may occur on a variety of crystallographic planes.

Transformation of a virtual or monotropic mesophase of the monomeric structural unit .

Transformation of a, -unsaturated carbonyl compounds having an allylsilyl group.

Transformation of a.oo-difunctional pIB into a chloro-terminated macroinitiator followed by the ATRP of St

Transformation of acyl fluorides.

Transformation of adenosylcobyric acid into adenosylcobalamin. The pathway shown in this figure is highlighted with the aerobic pathway enzymes. The corresponding enzymes of the anaerobic pathway are shown in Table 1. It is likely that the a-ribazole is synthesized as a-ribazole phosphate and that the phosphate is removed from the final coenzyme form of cobalamin.

Transformation of aidicarb to aidoxycarb.

Transformation of ajmalicine to alkaloids with Corynanthe-type, Iboga-type, and Aspidosperma-type skeletons

Transformation of ajmaline . Reagents

Transformation of ajmaline ii. riboflavin, hv.

Transformation of alcohols into amines by a redox self-sufficient cascade of ADH-catalyzed alcohol oxidation and co-TA-catalyzed reductive amination. Application of alanine-DH

Transformation of aldehydes and ketones to a-hydroxy acetals.

Transformation of aldehydes to nitriles employing copper powder and ammonium salts.

Transformation of alkynes to nitriles using tert-buiyl nitrite as nitrogen source

Transformation of allenylidene-ruthenium into active indenylidene-ruthenium catalyst.



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