Carbon atoms, quaternary

Gem-dimethyl and spiro-cyclopropyl are useful to render a carbon atom quaternary and therefore resistant to metabolic attacks. 

Carbon atoms, quaternary s. Tetraalkylmethanes Carbon chain s. C-Chain Carbon dioxide... 

A major difficulty with the Diels-Alder reaction is its sensitivity to sterical hindrance. Tri- and tetrasubstituted olefins or dienes with bulky substituents at the terminal carbons react only very slowly. Therefore bicyclic compounds with polar reactions are more suitable for such target molecules, e.g. steroids. There exist, however, several exceptions, e. g. a reaction of a tetrasubstituted alkene with a 1,1-disubstituted diene to produce a cyclohexene intermediate containing three contiguous quaternary carbon atoms (S. Danishefsky, 1979). This reaction was assisted by large polarity differences between the electron rich diene and the electron deficient ene component. 

Two adjacent tertiary carbon atoms 730-920 770-725 Often a band at 530-524 cm indicates presence of adjacent tertiary and quaternary carbon atoms. 

Solids present in oil and synthetic muds must be kept wet with the nonaqueous phase to prevent coagulation and settling and mud instabiUty. Oil-wetting agents are normally incorporated in the basic mud package. These materials are typically amines or quaternary ammonium salts having hydrocarbon chains of 10 or more carbon atoms. They also render clays or lignites oil-wet for use in viscosity and filtration control (128). 

Higher order aUphatic quaternary compounds, where one of the alkyl groups contains - 10 carbon atoms, exhibit surface-active properties (167). These compounds compose a subclass of a more general class of compounds known as cationic surfactants (qv). These have physical properties such as substantivity and aggregation ia polar media (168) that give rise to many practical appHcations. In some cases the ammonium compounds are referred to as iaverse soaps because the charge on the organic portion of the molecule is cationic rather than anionic. 

Alkylbenzyldimethyl quaternaries (ABDM) are used as disinfectants (49) and preservatives. The most effective alkyl chain length for these compounds is between 10 and 18 carbon atoms. Alkyltrimethyl types, alkyl dimethylbenzyl types, and didodecyl dimethyl ammonium chloride [3401-74-9] exhibit excellent germicidal activity (151—159). Dialkyldimethyl types are effective against anaerobic bacteria such as those found in oil wells (94—97). One of the most effective and widely used biocides is didecyl dimethyl ammonium chloride [7173-57-5]. 

Carbon atoms are classified according to their degree of substitution by other carbons. A primary carbon is directly attached to one other carbon. Similarly, a secondary carbon is directly attached to two other carbons, a tertiary carbon to three, and a quaternary carbon to four. Alkyl groups are designated as primary, secondary, or tertiary according to the degree of substitution of the carbon at the potential point of attachment. 

Nucleophilic attack at a carbon atom, followed by a mesomeric shift to make a nitrogen atom quaternary, has been known for many years. The best example is the formation of 1,3,3-trisubstituted 3 -indole salts by the action of alkyl halides on 1,3-disubstituted indoles. 

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