Tertiary amines Subject

This was ihe first investigation of stereoselective formation of geometric isomers of tertiary amines. The authors suggested most enamine systems should be subject to considerable stereochemical control. 

Benzylic quaternary ammonium salts, when treated with alkali metal amides, undergo a rearrangement called the Sommelet-Hauser rearrangementSince the product is a benzylic tertiary amine, it can be further alkylated and the product again subjected to the rearrangement. This process can be continued around the ring until an ortho position is blocked. ... 

The seco amide alkaloids have been subjected to various transformations, mainly for structure elucidation purposes. When treated with lithium aluminium hydride, arnottianamide (206) was converted to the tertiary amine, deoxyarnottianamide (224), which on methylation with the Rodionow reagent gave deoxy-O-methylarnottianamide (225) (172,175). Arnottianamide (206) could be O-acetylated (174) as well as O-methylated with diazomethane in HMPA (172). Isoarnottianamide (208) was O-methylated to trimethoxy derivative 226, which under Bischler-Napieralski conditions recyclized to the benzophenantridine alkaloid, chelilutine (227) (176) (Scheme 33). 

The use of m-CPBA allows the formation of nitrones in the oxidation of tertiary amines. The resulting amines A-oxides are subject to either Cope or Meisenheimer rearrangements, providing formation of nitrones. Thus, the generated corresponding nitrones in the oxidation of bicyclic aziridines give nitrones as a result of a Meisenheimer rearrangement (Scheme 2.14) (93). 

The starting benzothiazole carboxylic ester 387 was subjected to a Anamination by using mesityl hydroxylamine to give an A -amino salt 388, which was treated with a tertiary amine to give the deprotonated intermediate 389. This species when reacted with phenylisocyanate yielded the final product 390 in moderate yield <2001JOC8528>. 

The phosphonium and carbenium salts are efficient reagents for activating and coupling A-alkoxycarbonylamino acids as well as peptide acids. However, the requirement for tertiary amine to effect the reaction has several implications. The base renders hydroxyl groups subject to acylation. Hence, the side chains of serine and threonine and any hydroxymethyl groups of a resin that have not been derivatized... 

Recently, Turner et al. have shown tertiary amines can also be used as substrates by using a further variant of MAO-N (MAO-N-D5) which had also been developed by directed evolution techniques (Scheme 2.33). For example, racemic N-methyl-pyrrolidine 65 was subjected to deracemization, via the intermediate iminium ion... 

The chemical behavior and reactions of pyrrolizidine derivatives were investigated for the most part during structural analysis of naturally occurring pyrrolizidine alkaloids and in the course of the syntheses of their degradation fragments there are several publications concerned specially with this subject. Pyrrolizidine derivatives are typical tertiary amines, and consequently their chemical behavior is a combination of the properties of tertiary amines and of those of the substituent functions. However, some peculiarities of the class can be explained only in terms of the configuration of the bicyclic system. 

Reduction of aldehydes and ketones. Earlier work on amine borane reagents was conducted mainly with tertiary amines and led to the conclusion that these borane complexes reduced carbonyl compounds very slowly, at least under neutral conditions, and that the yield of alcohols is low. Actually complexes of borane with primary amines, NHj or (CH3)3CNH2, reduce carbonyl compounds rapidly and with utilization of the three hydride equivalents. BH3 NH3 is less subject to steric effects than traditional complex hydrides. A particular advantage is that NH3 BH3 and (CH3)3CNH2 BH3 reduce aldehyde groups much more rapidly than keto groups, but cyclohexanone can be reduced selectively in the presence of aliphatic and aromatic acyclic ketones. 

Antihistaminics, being tertiary amines, are analysed after reaction with an analogous reagent [566] with pentafluorobenzyl chloroformate a derivative is formed with a high ECD response and good GC properties, e.g., on OV-17. Hucker and Miller [567] subjected amitriptyline and other tertiary amines to exhaustive methylation and analysed the products from the reaction (Hoffman). Whereas the initial substances gave considerable tailing on 3% of QF-1, the derivatives provided sharp and symmetric peaks. 

Tertiary amines may be used as the base in the Michaelis-Becker reaction with highly reactive substrates. This approach has the advantage of overcoming the common problem of the low solubility of the metal dialkylphosphonate salts 22. However, amines are used as the base in the Atherton-Todd syntheses of phos-phorochloridates 27 and phosphoramidates 28 (Scheme 16), pathways which may thus compete with the Michaelis-Becker reaction of highly chlorinated substrates under such conditions the precise mechanism of the Atherton-Todd reaction is a subject of debate.61... 

Combination of the reagents TiCU, BuaN, and TMSOTf, was reported to be effective for Claisen condensation, as exemplified in Eqs (42) and (43) [129]. When acyl-oxazolidinones were subjected to reaction with TiCU and a tertiary amine, homocoupling reaction at the a-position of the acyl group took place to give succinic acid derivatives [146], The lithium enolate of an ester or amide has been alkylated with an (N,C>)-acetal in the presence of Ti(0-/-Pr)4 (Eq. 44) [147,148]. 

Epoxy resins may be cured in the manner of polyadditions, i. e., homogeneously catalyzed by multifunctional amines and isocyanates, or cyclic anhydride, dicyan-diamide, or biguanide derivatives. On the other hand epoxy resins are also subject to homopolymerization. The catalysts represent Lewis bases, preferably tertiary amines, imidazoles, or ureas (the latter exclusively for the dicyandiamide curing)... 

---