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Amides carboxylates

A-/-Butyldimethylsilyl-7V-methyltrifluoroacetamide, CH3CN, 5 min, 97-100% yield.This reagent also silylates thiols, amines, amides, carboxylic acids, and enolizable carbonyl groups. [Pg.78]

Iminium Acyl Aldehyde Ester Amide Carboxylate Group 111... [Pg.397]

Biochemical tests are usually performed after pure cultures have been obtained. The standard indole, methyl red, Voges-Proskauer, citrate, and litmus milk tests may be used to show important physiological characteristics. To study the functional diversity of bacteria, the utilization of carbohydrates, amines, amides, carboxylic acids, amino acids, polymers, and other carbon and nitrogen sources can be tested.28 Dilution-based most-probable number (MPN) techniques with phospholipid fatty acids as biomarkers have been employed for studying different bacterial species in lakes.40 The patterns of antibiotic resistance in bacteria isolated from natural waters have been useful for identifying sources of water pollution.34... [Pg.5]

A. T. Hagler, A. Lapicirella, Spatial Electron Distribution and Population Analysis of Amides, Carboxylic Acid, and Peptides, and Their Relation to Empirical Potential Functions , Biopolymers 1976, 1167-1200 A. T. Hagler, L. Leiserowitz, M. Tuval, Experimental and Theoretical Studies of the Barrier to Rotation about the N-C° and Ca-C Bonds ([Pg.369]

A question that may justifiably be raised here is whether these proofs of exclusive carbonyl protonation of carboxylic acids in concentrated and anhydrous acids necessarily imply the dominance of this form in dilute acid. Evidence that this is not so for amides has been discussed on pages 328 ff. It is possible that the alternative protonated form of carboxylic acids [201] is dominant in aqueous acid, but as the overall extents of protonation are small, it is not detectable by any spectroscopic method. Unlike amides, carboxylic acids become measurably protonated in quite concentrated acid (>60% sulphuric acid), which would tend to favour the formation of the protonated form with a delocalized charge. The form [201]... [Pg.367]

Use of a hydrocarbon solvent such as cyclohexane can discriminate these compounds either as the only measured value or as a value to be subtracted from the octanol value (Alog P) [19-21]. Unfortunately, cyclohexane is a poor solvent for many compounds and does not have the utility of octanol. Groups which hydrogen bond and attenuate actual membrane crossing compared to their predicted ability based on octanol are listed in Figure 1.4. The presence of two or more amide, carboxyl functions in a molecule will significantly impact on membrane crossing ability and will need substantial intrinsic lipophilicity in other functions to provide sufficient hydrophobicity to penetrate the lipid core of the membrane. [Pg.7]

A series of solid-state reactions has been explored by Kaupp et al., in which gaseous amines were reacted with aldehydes to give imines. Analogous reactions with solid anhydrides, imides, lactones or carbonates, and isothiocyanates were used to give, respectively, diamides or amidic carboxylic salts or imides, diamides, carbamic acids, and thioureas [24]. In general the yields were found to be quantitative. Ammonia and other gaseous amines, in particular methyl-amine, have also been shown to aminolyse thermoplastic polycarbonates [25]. [Pg.76]

By studying the nucleophilic opening of 2,3-epoxy carboxylic acid derivatives it has been found that the regioselectivity was dependent on the acid function (ester, amide, carboxylate), as well as on the nucleophile [78]. In the examples... [Pg.140]

Alkyl- or 3-aryl-2,4-oxazolidinediones via photochemical cyclization, ° organonickel-mediated carbonylation, ° cyclization of A-alkenyl-a-acet-amides, ° carboxylation and cyclization of 2-propynamides, °" cyclization of (9-carbamates of a-hydroxy acetic acids and esters,cyclization of a-hydroxy acetamides,and catalytic asymmetric dihydroxylation (ADH) of A-alkenoyl-2-oxazolidinones. ... [Pg.90]

Carboxylic Amides. Carboxylic amide nonionic surfactants are condensation products of fatty acids and hydroxyalkyl amines. [Pg.252]

KETONES, ALDEHYDES, AMIDES, CARBOXYLIC ACIDS, AND ESTERS ALL CONTAIN A CARBONYL CROUP... [Pg.407]

The carbonyl group consists of a carbon atom double-bonded to an oxygen atom. It occurs in the organic compounds known as ketones, aldehydes, amides, carboxylic acids, and esters. [Pg.407]

Amine Acid anhydride Amide Carboxylate salt... [Pg.866]


See other pages where Amides carboxylates is mentioned: [Pg.590]    [Pg.40]    [Pg.238]    [Pg.216]    [Pg.494]    [Pg.711]    [Pg.383]    [Pg.130]    [Pg.188]    [Pg.4]    [Pg.201]    [Pg.188]    [Pg.154]    [Pg.152]    [Pg.211]    [Pg.850]    [Pg.219]    [Pg.187]    [Pg.358]    [Pg.353]    [Pg.368]    [Pg.95]    [Pg.103]    [Pg.405]    [Pg.1204]    [Pg.128]    [Pg.709]   
See also in sourсe #XX -- [ Pg.798 ]

See also in sourсe #XX -- [ Pg.806 ]




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0-Diketones carboxylic acid amide

1.3- Heterocyclics carboxylic acid amide

A- carboxylic acid amides

Acyl imidates carboxylic acid amides

Acylamines (s. a. N-Acyl Carboxylic acid amides

Acylisocyanates carboxylic acid amide

Acylureas carboxylic acid amide

Alcohols carboxylic acid amide

Aldehydes (s. a. Aldehyde carboxylic acid amide

Aldehydes (s. a. Formyl carboxylic acid amides

Aldoximes carboxylic acid amide

Alkylation of Aldehydes, Esters, Carboxylic Acids, Amides, and Nitriles

Amidation of carboxylic

Amidation of carboxylic acids

Amidation of carboxylic acids with

Amidation, carboxylic acids

Amide . . . s. a. Carboxylic

Amide Carboxylic acid derivatives

Amide carboxyl and

Amide ether carboxylates

Amide formation, from a carboxylic

Amide formation, from a carboxylic acid

Amide formation, from a carboxylic acid and urea

Amide... s. a. Carboxylic acid

Amides carboxylic acid conversion

Amides from ammonium carboxylates

Amides from carboxylic acids

Amides from carboxylic anhydrides

Amides of Aromatic Carboxylic Acids

Amides s. Carboxylic acid

Amidines carboxylic acid amides

Amidinium salts carboxylic acid amides

Amines carboxylic acid amides

Aryl halides carboxylic acid amide

Azomethines carboxylic acid amides

Barbituric acids carboxylic acid amide

Benzoxazoles carboxylic acid amide

Carbodiimides carboxylic acid amides

Carbonyl compounds Aldehydes Amides Carboxylic acid

Carbonyl group Aldehydes Amides Carboxylic

Carbonyl group Aldehydes Amides Carboxylic acid

Carboxyl group amides

Carboxylate salts amides, hydrolysis

Carboxylate-amide base systems

Carboxylic Acid Amide (CAA, Fungicides

Carboxylic Acids, Esters, Amines, and Amides

Carboxylic Acids, Esters, Chlorides, Anhydrides, Amides, and Nitriles

Carboxylic Acids, Esters, and Amides

Carboxylic acid alkoxymethylamides amides

Carboxylic acid amid

Carboxylic acid amid 0-aminoketones

Carboxylic acid amid 3 molecules)

Carboxylic acid amid 4,5-dihydroxy

Carboxylic acid amid 7-halogeno- (from

Carboxylic acid amid Dimethylformamide)

Carboxylic acid amid N-subst.

Carboxylic acid amid acetamide

Carboxylic acid amid acetyl halides

Carboxylic acid amid acylamines

Carboxylic acid amid alcohols, prim

Carboxylic acid amid aldehydes

Carboxylic acid amid aldehydes, synthesis with

Carboxylic acid amid amides

Carboxylic acid amid amidines

Carboxylic acid amid aminocarboxylic acids

Carboxylic acid amid cyclopropane ring

Carboxylic acid amid esters

Carboxylic acid amid ethylene derivs

Carboxylic acid amid group participation

Carboxylic acid amid halides

Carboxylic acid amid hindered

Carboxylic acid amid hydrocarbons

Carboxylic acid amid hydrocarbons, synthesis with

Carboxylic acid amid iminoesters

Carboxylic acid amid isocyanates

Carboxylic acid amid ketones, hydrolysis

Carboxylic acid amid ketones, synthesis

Carboxylic acid amid malonic

Carboxylic acid amid mixed

Carboxylic acid amid nitriles

Carboxylic acid amid polyamide

Carboxylic acid amid synthesis

Carboxylic acid amid synthesis with addition

Carboxylic acid amid vinylogous

Carboxylic acid amide aldehydes

Carboxylic acid amide amides

Carboxylic acid amide anhydrides

Carboxylic acid amide azides

Carboxylic acid amide chlorides

Carboxylic acid amide complexes

Carboxylic acid amide esters

Carboxylic acid amide fluorides

Carboxylic acid amide fungicides

Carboxylic acid amide hydrazides, subst

Carboxylic acid amide iminoesters

Carboxylic acid amide mixed

Carboxylic acid amide nitriles

Carboxylic acid amide peptides

Carboxylic acid amide phosphites

Carboxylic acid amide rearrangement

Carboxylic acid amides

Carboxylic acid amides Grignard synthesis

Carboxylic acid amides acids

Carboxylic acid amides and nitriles

Carboxylic acid amides compds

Carboxylic acid amides from ethylene derivs

Carboxylic acid amides ketene addition

Carboxylic acid amides reactivity with nucleophiles

Carboxylic acid amides tetrahedral intermediates

Carboxylic acid amides with

Carboxylic acid amides, synthesi

Carboxylic acid azides amide synthesis

Carboxylic acid derivatives Acyl chlorides Amides

Carboxylic acid derivatives chlorides Amides Anhydrides

Carboxylic acid derivatives synthesis amides

Carboxylic acid dimethyl amides

Carboxylic acids amide adducts

Carboxylic acids amide formation

Carboxylic acids amide formation from

Carboxylic acids amide synthesis

Carboxylic acids by amide hydrolysis

Carboxylic acids hydroxide + amides

Carboxylic acids to amides

Carboxylic acids, amidation catalyzed

Carboxylic acids, amides prepared

Carboxylic acids, amides prepared bromination

Carboxylic acids, amides prepared chlorination

Carboxylic acids, amides prepared preparation

Carboxylic acids, amides prepared reactions

Carboxylic acids, amides prepared solubility

Carboxylic acids, functional derivatives Acid anhydrides, Amides, carbonic

Carboxylic amide derivative

Carboxylic amide, synthesis

Carboxylic amides

Carboxylic amides

Carboxylic amides, reactivity

Chemistry of Carboxylic Acid Amides

Conformational Analysis of Carboxylic Esters and Amides

Conformational Properties of Carboxylic Acids and Amides

Diacylamines carboxylic acid amides

Enamines (s. a. Aminomethylene carboxylic acid amides

Ethylene derivatives carboxylic acid amide

Formation of Carboxylic Acids, Esters, and Amides

Functional groups carboxylic amides

Halides carboxylic acid amides

Hofmann degradation carboxylic acid amide

Homologation Carboxylic acid, ester, amide

Hydrocarbons, hydrocarbon carboxylic acid amides

Imidazole-4-carboxylic acid amides

Imidazolium salts carboxylic acid amide

Indole-2-carboxylic acid amides

Isocyanates carboxylic acid amides

Isothiocyanates carboxylic acid amide

Keteneacylals carboxylic acid amide

Ketenimines carboxylic acid amide

Ketocarboxylic acid amides carboxylic acids

Ketones, Aldehydes, Amides, Carboxylic Acids, and Esters All Contain a Carbonyl Croup

Lactams carboxylic acid amides

Lipase carboxylic acid amides

Malyngolide carboxylic amides

Nickel complexes carboxylic acid amide

Of carboxylic acid amides

Oxidation carboxylic acid amides

Oximes carboxylic acid amides

Palladium complexes carboxylic acid amide

Part A Carboxylic Acids, Esters and Amides

Peptides (s. a. Carboxylic acid amides, subst

Phosphorodithioates containing carboxylic acid ester and amide groups

Piperidine-4-carboxylic acid amide

Primary carboxylic amide

Pyridine carboxylic acid amide

Pyridine-3-carboxylic acid amides nicotinamide

Pyrimidines carboxylic acid amides

Pyrolysis carboxylic acid amides

Secondary carboxylic amide

Synthesis of Amines from Carboxylic Amides

Tertiary carboxylic amide

Transamidation carboxylic acid amides

Transamidation carboxylic acid amides from

Ureas carboxylic acid amides

Urethans carboxylic acid amides

Vinylogous carboxylic amides

Vinylogs carboxylic acid amides

Weinreb amides from carboxylic acids

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