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Addition derivatives

A monograph (1) covers the pioneering period of sulfa dmg development and describes over 5000 sulfanilamide derivatives, their preparation, properties, trade names, and biological testing. This review is remarkably complete through 1944. Several thousand additional derivatives have been made since, but no comparable coverage is available. A definitive account of medical appHcations up to 1960 has been pubHshed (2), and a review of experimental antibacterial aspects has been made (3). Chapters on general aspects of sulfonamides and sulfones have appeared (4,5). A review of the clinical efficacy of trimethoprim—sulfamethoxazole has been pubHshed (6). [Pg.463]

Note added in proof The compounds described as derivatives of 2,4-dichlorothiophene are derivatives of 2,3-dichlorothiophene/ Additional derivatives of 2,3-dichIorothiophene have been pre-pared. "" ... [Pg.60]

Some additional derivatives containing extended 7t-systems in place of the benzene nucleus are naphthalene, anthracene (2,3-Ac) and phenanthrene (9,10-Phc). They also belong to the phthalocyanine family. For the naphthalene system two types of macrocyclcs, the 1,2-naph-thalocyanine (1,2-Nc) and the 2,3-naphthalocyanine (2,3-Nc), are known. [Pg.718]

The preparation of two additional derivatives of amino acids having pendant nucleic acid bases was reported successively ( 14, 15 ). [Pg.365]

In prineiple, this additional derivation also starts from the many-fermion Hamiltonian given in equation (75). As discussed earlier, extension of this equation to moleeules usually is done by imposing the requirement that some of these partieles are nuelei whieh are assumed to be fermions. An alternative, but less rigorous approaeh to introduce nuclei is to eonsider them as an external perturbation whieh modifies the external veetor and sealar potential in equation (75). Further approximations ean be made for non-dynamical properties by invoking the elamped nuelei approximation. For such a situation the external vector potential A can be written as... [Pg.462]

The red-emitting rhodamine derivatives are constructed around the same basic xanthene framework as is fluorescein (2). Tetramethylrhodamine isothiocyanate (TRITC) has been widely employed for immunofluorescence. Additional derivatives of rhodamine available for conjugation to antibodies include lissamine rhodamine sulfonyl chloride (RB-200-SC), rhodamine B isothiocyanate (RBITC), rhodamine X isothiocyanate (XRITC), and Texas... [Pg.101]

The reconstruction functionals, derived in the previous section through the particle-hole duality, may also be produced through the theory of cumulants [21,22,24,26,39,55-57]. We begin by constructing a functional whose derivatives with respect to probe variables generate the reduced density matrices in second quantization. Because we require that additional derivatives increase the number of second quantization operators, we are led to the following exponential form ... [Pg.176]

Gayathri SS, Patnaik A (2006) Electrical rectification from a fullerene[60]-dyad based metal-organic-metal junction. Chem Commun (Cambridge, UK) 1977-1979 Matino F, Arima V, Piacenza M et al (2009) Rectification in supramolecular zinc porphyrin/ fulleropyrrolidine dyads self-organized on gold(lll). Chemphyschem 10 2633-2641 Acharya S, Song H, Lee J et al (2009) An amphiphilic Cgo penta-addition derivative as a new U-type molecular rectifier. Org Electron 10 85-94... [Pg.166]

Diammino-stannic Fluoride, [Sn(NFI3)2]F4, is formed if stannic fluoride and ammonia are heated together in a sealed tube to a temperature of 120° C. Both the monammine and the diammine are soluble in water, the solutions becoming cloudy due to decomposition. Stannic fluoride also forms addition derivatives with the bases pyridine and quinoline. [Pg.65]

The first well-eharacterised ammonia additive derivative of chromium was prepared by Fremy in 185S.2 Shortly after, in 1802, the compound was examined by Cleve,3 who prepared a number of compounds of chromic salts and ammonia. He proved the composition of these substances and endeavoured, in so far as the knowledge of that time allowed, to explain their constitution. [Pg.74]

The potassium salt, [Cr(NH3)2(SCN)4JK, crystallises in red cubes which are easily soluble in water, and if treated with iodine in potassium iodide it forms the addition derivative, [Cr(NH3)2(SCN)4]K.I.3... [Pg.112]

Two additional derivatives were prepared using bis( V-acrylolyaminomcthanc and divinylbenzene as crosslinking agents as illustrated below. [Pg.78]

Additional derivatives of the current invention are described by Nesvadba et al. (1). [Pg.324]

D-Glutamic acid-g-(t-butyl)ester N-carboxy anhydride was previously polymerized by Fujimoto et al. (1) in a l,2-dichloroethane/l,4-dioxane mixture using sodium 4-methyl-2-pyrrolidone as initiator. Additional derivatives were... [Pg.478]

Additional derivatives of the current were prepared by the authors (1) in an earlier investigation and are discussed. [Pg.484]

No naturally occurring 1,2,4-thiadiazole having been reported so far, all compounds are of synthetic origin. The parent of the series, 1,2,4-thiadiazole, was first synthesized in 1955s by the sequence of reactions 8->9—>-10->-2,B 6 but remains relatively inaccessible. Because of its sensitivity it is not a practicable starting material for the preparation of derivatives these are therefore always built up directly by suitable cyclization reactions and subsequent modification of the substituentB as required. This section is confined to direct syntheses the numerous interconversions that furnish additional derivatives from the preformed 1,2,4-thiadiazole nucleus are considered with the chemical properties of the individual classes of compounds. [Pg.122]


See other pages where Addition derivatives is mentioned: [Pg.573]    [Pg.224]    [Pg.18]    [Pg.22]    [Pg.204]    [Pg.11]    [Pg.127]    [Pg.36]    [Pg.339]    [Pg.50]    [Pg.426]    [Pg.278]    [Pg.176]    [Pg.136]    [Pg.8]    [Pg.205]    [Pg.62]    [Pg.32]    [Pg.35]    [Pg.203]    [Pg.34]    [Pg.40]    [Pg.134]    [Pg.143]    [Pg.157]    [Pg.249]    [Pg.260]    [Pg.500]    [Pg.547]    [Pg.627]    [Pg.366]    [Pg.323]   
See also in sourсe #XX -- [ Pg.67 ]




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1.1- Dithiolate derivatives, sulfur addition

3- Oxazolin-5-ones, 2-arylidene derivatives conjugate addition

7-Azaindole derivatives, addition

Acylpalladium derivatives oxidative addition

Adamantyl derivatives Addition-elimination

Adamantyl derivatives addition reactions

Addition Reactions of Benzene Derivatives

Addition Reactions using Iminium Ions Derived from Hydrazines, Hydroxylamines and Sulfinamides

Addition benzene derivatives

Addition derivatives, startg

Addition of Hydrazoic Acid and Its Derivatives to Non-Activated Olefins

Addition of hydrogen cyanide derivatives

Addition of hydrogen sulfide and its derivatives

Addition reactions derivatives

Addition to Carboxylic Acids and Derivatives

Additional Common Derived Units of SI

Additional Useful Relations Between Partial Derivatives

Additions to Imine Derivatives

Additions to Imine Derivatives Bearing N-Bound Auxiliaries

Additions with Organocopper Reagents Derived from CuCN-2LiBr-Based Active Copper

Additives lignin derived

Aldehydes, addition derivatives

Aldehydes, addition derivatives Grignard reaction

Aldehydes, addition derivatives ammonia reaction

Aldehydes, addition derivatives chlorination

Aldehydes, addition derivatives condensation reactions

Aldehydes, addition derivatives defined

Aldehydes, addition derivatives oxidation

Aldehydes, addition derivatives preparation

Aldehydes, addition derivatives rates

Aldehydes, addition derivatives reactions

Aldehydes, addition derivatives sodium bisulphite reaction

Alkynes addition of sulphur-derived

Allyltin derivatives nucleophilic addition

Amines, Amine Derivatives, Congeners, and Acidic Additives

Aryl derivatives oxidative addition

Asymmetric Addition to Imine Derivatives

Asymmetric conjugate addition BINOL derivatives

BINOL derivatives addition with

Benzene derivatives addition reactions

Binucleating systems based on 4-substituted 2,6-dicarbonylphenol derivatives and diamines containing additional donor atoms or groups

Biomass derivatives fuel additives

Borane, derivatives addition reactions with aldehydes

Carbonyl derivatives amine addition

Carboxylic Acids and Their Derivatives Nucleophilic Addition-Elimination at the Acyl Carbon

Carboxylic acid derivatives addition

Carboxylic acid derivatives addition-elimination

Cinchonidine-derived catalysts addition with

Concerted addition benzyl derivatives

Conjugate addition carboxylic acid derivatives

Conjugate additions derivatives

Cyclohexane derivatives 1,3-dipolar additions

Electrophilic Addition to Acetylene Derivatives

Electrophilic Addition to Allene Derivatives

Enzyme-catalyzed aldol addition derivatives

Ethylene derivatives addition polymerization

Ethylene derivatives synthesis with addition

Ethylene derivs with addition

Furan derivatives, additions

Furanose derivatives, additive

Imino derivatives, addition reactions

Ketones, addition derivatives

Ketones, addition derivatives Grignard reaction

Ketones, addition derivatives chlorination

Ketones, addition derivatives cyclic

Ketones, addition derivatives defined

Ketones, addition derivatives oxidation

Ketones, addition derivatives preparation

Ketones, addition derivatives reactions

Malonic acid derivatives, additions

Markovnikov additions alkyne derivatives

Methylol derivatives Addition

Methylol derivatives Addition reactions

Michael addition retro-, acid derivative

Naphthol derivatives, addition with

Nitrones, addition carbohydrate-derived

Nucleophilic Addition of Ammonia and Its Derivatives

Nucleophilic addition by allyltin derivatives

Nucleophilic addition carboxylic acid derivatives

Nucleophilic addition reactions carboxylic acid derivatives

Nucleophilic addition reactions derivatives

Nucleophilic addition-elimination acid derivatives

Oxidative addition allylic alcohol derivatives

Oxidative addition phenol derivatives

Oxime derivatives, oxidative addition

Papermaking additives, starch derivatives

Potential-Derived Monopole Models with Additional Nonatomic Sites

Prolinol-derived catalysts Michael addition

Prolinol-derived catalysts addition

Quinidine-derived catalysts addition

Quinine-derived catalysts Michael addition

Sulfonic acids, addition derivatives

Thiourea derived catalysts Michael addition

Thiourea derived catalysts addition

Transition-metal derivatives oxidative addition methods

Triple bonds s. Acetylene derivatives, Addition

Tryptophane-derived catalysts, addition with

Urea-derived catalysts addition

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