Add to ORKGNitrile imines are considered as the versatile reactive intermediates and are recognized as a linear-type 1,3-dipoles extensively used in 1,3-dipolar cycloaddition reactions for constructing biologically potent five membered heterocycles. This review article comprises the brief history, up to date information about the various methods employed for the generation, stability, reactivity and synthetic applications of nitrile imines. The stereochemistry of the products formed with the use of nitrile imines and biological activity associated with the cycloadducts formed was also presented
Caballero, J (Caballero, Julio). Univ Talca, Fac Ingn Bioinformat, Ctr Bioinformat & Simulac Mol, C...
1-3 dipolar cycloaddition is the union of a 1-3 dipole, a-b-c, with a system containing a multiple b...
The objective of this investigation was to develop a new synthetic method for the asymmetric synthes...
Heterocycles, cyclic organic molecules containing atoms other than carbon, have displayed a wide and...
The nitrile imine 1,3-dipole is a versatile intermediate with a diverse range of applications from c...
The concept of 1,3‐dipolar cycloaddition was developed, starting in the late 1950s, largely by Rolf ...
1,3-Dipolar cycloadditions are a versatile method for the formation of five membered heterocyclic ri...
Stereoselective 1,3-dipolar cycloadditions of nitrilimines represents a useful tool in the obtainme...
An in depth account of intramolecular 1,3-dipolar cycloadditions involving dipoles such as nitrile o...
The multiform intramolecular reactivity of nitrilimines is presented in a systematic way, giving emp...
Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Chemistry, 2003.Vita.Includes bibli...
A convenient method for the synthesis of 1,2,4-triazol-3-imines through a selective, formal, 1,3-dip...
A series of γ-substituted α-methylidene-γ-butyrolactone derivatives underwent regiospecific 1,3-dipo...
Nitrilium betaine 1,3-dipoles are ubiquitous reagents in organic chemistry, with applications rangin...
Nitrile imine cycloaddition to hydantoins containing an exocyclic C=C double bond has been previousl...
Caballero, J (Caballero, Julio). Univ Talca, Fac Ingn Bioinformat, Ctr Bioinformat & Simulac Mol, C...
1-3 dipolar cycloaddition is the union of a 1-3 dipole, a-b-c, with a system containing a multiple b...
The objective of this investigation was to develop a new synthetic method for the asymmetric synthes...
Heterocycles, cyclic organic molecules containing atoms other than carbon, have displayed a wide and...
The nitrile imine 1,3-dipole is a versatile intermediate with a diverse range of applications from c...
The concept of 1,3‐dipolar cycloaddition was developed, starting in the late 1950s, largely by Rolf ...
1,3-Dipolar cycloadditions are a versatile method for the formation of five membered heterocyclic ri...
Stereoselective 1,3-dipolar cycloadditions of nitrilimines represents a useful tool in the obtainme...
An in depth account of intramolecular 1,3-dipolar cycloadditions involving dipoles such as nitrile o...
The multiform intramolecular reactivity of nitrilimines is presented in a systematic way, giving emp...
Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Chemistry, 2003.Vita.Includes bibli...
A convenient method for the synthesis of 1,2,4-triazol-3-imines through a selective, formal, 1,3-dip...
A series of γ-substituted α-methylidene-γ-butyrolactone derivatives underwent regiospecific 1,3-dipo...
Nitrilium betaine 1,3-dipoles are ubiquitous reagents in organic chemistry, with applications rangin...
Nitrile imine cycloaddition to hydantoins containing an exocyclic C=C double bond has been previousl...
Caballero, J (Caballero, Julio). Univ Talca, Fac Ingn Bioinformat, Ctr Bioinformat & Simulac Mol, C...
1-3 dipolar cycloaddition is the union of a 1-3 dipole, a-b-c, with a system containing a multiple b...
The objective of this investigation was to develop a new synthetic method for the asymmetric synthes...