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Yields of cracking products from cycle I to infinity

Yields of cracking products of the round cracking process in the steady state

Yields of ct-Arylated Ketones Formed in Photostimulated Reaction of Ketone Enolates with Aryl

Yields of cumene transformation products over oxides with evaporated metals reaction temperature 823

Yields of cyclized products vs ring size

Yields of cycloaddition of azides R-N3 to substituted methyl acrylates .

Yields of cycloalkyne adducts. I

Yields of cyclopropanation of various olefins by diazoacetic esters in the presence of Rh2 b

Yields of cyclopropanation of various olefins by diazoacetic esters in the presence of Rhj

Yields of Cyclopropane Formed Directly During Formation of Cyclopropylmagnesium Bromide in the Reaction of Cyclopropane with Magnesium

Yields of Cyclopropanes 12.

Yields of damaged bases unit

Yields of Degradation Products after Oxidizing 6,6 Bicreosol a

Yields of Diaiyl Sulfides Formed in Photostimulated Reaction of Aienethiolates with Aryl and Heteroaryl

Yields of Dialkyl Arylphosphonates Formed in the Photostimulated Reaction of Dialkyl Phosphite Ions with Aryl Halides

Yields of different tertiary homoallylic alcohols from Barbier reactions of crotyl chloride, magnesium and diethyl carbonate in various solvents and solvent mixtures

Yields of different tertiary homoallylic alcohols from Barbier reactions of crotyl halides, magnesium and ethyl ethanoate in several different solvents and solvent mixtures

Yields of dijfevent stars with masses between 13 and 70 Mq

Yields of Dimers and Trimers from Styrene and 2-Vlnyl thiophene

Yields of each enzyme-catalyzed glycosylation step

Yields of enzyme synthesis in vitro

Yields of esters from the decomposition of the nitroso-amides .

Yields of Ethyl Acetate Extracts After Acidic Treatment of Glucose, Xylose, and Glucuronic Acid at 300 C

Yields of Ethylene and C6 Cyclic Compounds from Butadiene

Yields of example radiopharmaceuticals labeled with fluoride ion using nucleophilic substitution reactions performed in protic solvent systems compared with literature methods utilizing aprotic organic solvents



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