Enantiopure Nß-Fmoc-amino alkyl isonitriles and amino acid esters have been employed as building blocks in Ugi four-component reaction (U-4CR) to yield 1,1'-iminodicarboxylated peptidomimetics. By employing trifluoroacetic acid as one of the components, a different outcome has been observed and rationalized. Ugi products are obtained as trifluoroacetamide adducts, which on further reaction under mild acidic conditions lead to the title compounds. The method has also been proven to be useful for the preparation of ethyl, benzyl and tert-butyl esters
Synthetically useful Nb-Fmoc amino alkyl isonitriles are prepared conveniently from Nb-Fmoc amino a...
The purpose of this thesis was to access to chiral heterocycles such as isoxazolidin-5-ones by makin...
Stereocontrolled synthesis of some amino acid-based carbocyclic nucleoside analogs containing ring ...
Enantiopure N β-Fmoc-amino alkyl isonitriles and amino acid esters have been employed as building b...
The Ugi-4C reaction employing Nβ-protected-amino alkyl isonitrile, amino acid ester, aldehyde, and ...
An Ugi multicomponent reaction with chiral cyclic amino acids, benzyl isocyanide and cyclic ketones ...
An Ugi multicomponent reaction with chiral cyclic amino acids, benzyl isocyanide and cyclic ketones ...
aminoalcohols, isocyanides, multicomponent reactions, peptidomimetics, Ugi reactio
An efficient synthesis of Nα-protected amino nitriles from Nα-protected amino acid amides employing ...
In the last decade a change of thought has taken place in the pharmaceutical industry which has led ...
The Ugi four-component reaction (Ugi-4CR) undoubtedly is the most prominent multicomponent reaction ...
The synthesis of α-ureidopeptidomimetics employing a simple, mild and straight forward route startin...
We describe herein our recent explorations in the field of isonitrile chemistry. An array of broadly...
Sequential combination of Ugi-MCR and click chemistry has been employed for the synthesis of triazol...
<div><p></p><p>This article describes the synthesis of new peptomers through a simple and efficient ...
Synthetically useful Nb-Fmoc amino alkyl isonitriles are prepared conveniently from Nb-Fmoc amino a...
The purpose of this thesis was to access to chiral heterocycles such as isoxazolidin-5-ones by makin...
Stereocontrolled synthesis of some amino acid-based carbocyclic nucleoside analogs containing ring ...
Enantiopure N β-Fmoc-amino alkyl isonitriles and amino acid esters have been employed as building b...
The Ugi-4C reaction employing Nβ-protected-amino alkyl isonitrile, amino acid ester, aldehyde, and ...
An Ugi multicomponent reaction with chiral cyclic amino acids, benzyl isocyanide and cyclic ketones ...
An Ugi multicomponent reaction with chiral cyclic amino acids, benzyl isocyanide and cyclic ketones ...
aminoalcohols, isocyanides, multicomponent reactions, peptidomimetics, Ugi reactio
An efficient synthesis of Nα-protected amino nitriles from Nα-protected amino acid amides employing ...
In the last decade a change of thought has taken place in the pharmaceutical industry which has led ...
The Ugi four-component reaction (Ugi-4CR) undoubtedly is the most prominent multicomponent reaction ...
The synthesis of α-ureidopeptidomimetics employing a simple, mild and straight forward route startin...
We describe herein our recent explorations in the field of isonitrile chemistry. An array of broadly...
Sequential combination of Ugi-MCR and click chemistry has been employed for the synthesis of triazol...
<div><p></p><p>This article describes the synthesis of new peptomers through a simple and efficient ...
Synthetically useful Nb-Fmoc amino alkyl isonitriles are prepared conveniently from Nb-Fmoc amino a...
The purpose of this thesis was to access to chiral heterocycles such as isoxazolidin-5-ones by makin...
Stereocontrolled synthesis of some amino acid-based carbocyclic nucleoside analogs containing ring ...