Direct preparation of tertiary amines in which two substituents are aromatic is described. In the presence of either the inorganic base sodium tert-butoxide or the sterically hindered organic base diisopropylethylamine, the alkylation of secondary diarylamines is achieved smoothly. In contrast to methods previously reported in the literature, this procedure is high-yielding and does not require the use of transition-metal catalysts or functional-group-intolerant hydride reductants.</p
Tertiary N-tosylamidines are readily reduced by an equimolar amount of lithium aluminium hydride to ...
Direct N‐alkylation of primary amines to secondary/tertiary amines and of secondary amines to tertia...
Herein, an efficient and green method for the selective synthesis of tertiary amines has been develo...
Direct preparation of tertiary amines in which two substituents are aromatic is described. In the pr...
Tertiary amines are utilized extensively as non-nucleophilic proton scavengers for a number of organ...
A simple and efficient method for the preparation of secondary N-alkylarylamines via reductive amina...
<p>In this article, direct <i>N</i>-alkylation of secondary amines with carboxylic acid is described...
Alkyl groups can be cleaved e.ciently and selectively from tertiary alkyl amines using propargyl chl...
A method for selective mono-N-alkylation of primary amines to produce secondary amines that are subs...
Three advanced methodologies for the preparation of extremely sterically hindered tertiary alkyl ami...
A number of tertiary N-allyl- and N-propargyl-substituted amines have been prepared by alkylation of...
The highly monoselective N-arylation of aromatic tertiary amines using a transition-metal-free appro...
The arylation of secondary acyclic amides has been achieved with diaryliodonium salts under mild and...
A protocol for the synthesis of α-tertiary amines was developed by iterative addition of carbon nucl...
The palladium-promoted deallylation of allylamines derived from primary and secondary amines is achi...
Tertiary N-tosylamidines are readily reduced by an equimolar amount of lithium aluminium hydride to ...
Direct N‐alkylation of primary amines to secondary/tertiary amines and of secondary amines to tertia...
Herein, an efficient and green method for the selective synthesis of tertiary amines has been develo...
Direct preparation of tertiary amines in which two substituents are aromatic is described. In the pr...
Tertiary amines are utilized extensively as non-nucleophilic proton scavengers for a number of organ...
A simple and efficient method for the preparation of secondary N-alkylarylamines via reductive amina...
<p>In this article, direct <i>N</i>-alkylation of secondary amines with carboxylic acid is described...
Alkyl groups can be cleaved e.ciently and selectively from tertiary alkyl amines using propargyl chl...
A method for selective mono-N-alkylation of primary amines to produce secondary amines that are subs...
Three advanced methodologies for the preparation of extremely sterically hindered tertiary alkyl ami...
A number of tertiary N-allyl- and N-propargyl-substituted amines have been prepared by alkylation of...
The highly monoselective N-arylation of aromatic tertiary amines using a transition-metal-free appro...
The arylation of secondary acyclic amides has been achieved with diaryliodonium salts under mild and...
A protocol for the synthesis of α-tertiary amines was developed by iterative addition of carbon nucl...
The palladium-promoted deallylation of allylamines derived from primary and secondary amines is achi...
Tertiary N-tosylamidines are readily reduced by an equimolar amount of lithium aluminium hydride to ...
Direct N‐alkylation of primary amines to secondary/tertiary amines and of secondary amines to tertia...
Herein, an efficient and green method for the selective synthesis of tertiary amines has been develo...