Add to ORKGA new synthetic protocol for the alkylation of N, N\u2032-disubstituted formamidines under Mitsunobu conditions is reported. The asymmetrical substitution of amidine substrates allowed investigation of the reaction trends
The Mitsunobu reaction is a mild way to convert an alcohol into a wide range of functionality.1 In g...
A variety of N-carbobenzoxy, N′-formyl gem-diaminoalkyl derivatives have been obtained through Golds...
Abstract Efficient one-pot three component reaction of aniline derivatives with cyanoamide and triet...
Chiral amino acid-derived formamides represent one of the most versatile components in multicomponen...
A Thesis Submitted to the Faculty of the Graduate School of the University of Kansas Lawrence for th...
A Thesis Submitted to the Faculty of the Graduate School of the University of Kansas Lawrence for th...
This thesis explores the synthesis and the reactivity of novel amidine salts resulting from various ...
This thesis explores the synthesis and the reactivity of novel amidine salts resulting from various ...
The amidinoethylation of alcohols takes place by the addition of sodium alkoxides 2 (R1 = Me, Et) to...
This report discusses research concerning synthetic applications of enaminoketones. The work may be ...
The amidinoethylation of amino compounds takes place by the addition of amines to the CC double bond...
A catalytic protocol for the base-mediated amidation of unactivated esters with amino alcohol deriva...
The Mitsunobu reaction is an important tool in carbocyclic nucleoside chemistry for the direct coupl...
The Mitsunobu reaction is an important tool in carbocyclic nucleoside chemistry for the direct coupl...
AbstractAn unexpected route for the synthesis of N,N-dialkyl formamidines has been reported by the r...
The Mitsunobu reaction is a mild way to convert an alcohol into a wide range of functionality.1 In g...
A variety of N-carbobenzoxy, N′-formyl gem-diaminoalkyl derivatives have been obtained through Golds...
Abstract Efficient one-pot three component reaction of aniline derivatives with cyanoamide and triet...
Chiral amino acid-derived formamides represent one of the most versatile components in multicomponen...
A Thesis Submitted to the Faculty of the Graduate School of the University of Kansas Lawrence for th...
A Thesis Submitted to the Faculty of the Graduate School of the University of Kansas Lawrence for th...
This thesis explores the synthesis and the reactivity of novel amidine salts resulting from various ...
This thesis explores the synthesis and the reactivity of novel amidine salts resulting from various ...
The amidinoethylation of alcohols takes place by the addition of sodium alkoxides 2 (R1 = Me, Et) to...
This report discusses research concerning synthetic applications of enaminoketones. The work may be ...
The amidinoethylation of amino compounds takes place by the addition of amines to the CC double bond...
A catalytic protocol for the base-mediated amidation of unactivated esters with amino alcohol deriva...
The Mitsunobu reaction is an important tool in carbocyclic nucleoside chemistry for the direct coupl...
The Mitsunobu reaction is an important tool in carbocyclic nucleoside chemistry for the direct coupl...
AbstractAn unexpected route for the synthesis of N,N-dialkyl formamidines has been reported by the r...
The Mitsunobu reaction is a mild way to convert an alcohol into a wide range of functionality.1 In g...
A variety of N-carbobenzoxy, N′-formyl gem-diaminoalkyl derivatives have been obtained through Golds...
Abstract Efficient one-pot three component reaction of aniline derivatives with cyanoamide and triet...