Rational synthesis of A<sub>2</sub>B-type <i>meso</i>-arylsubporphyrins has been accomplished by the condensation of triethylamine–tri-<i>N</i>-tripyrromethene–borane with acid chlorides. These subporphyrins are useful for evaluations of the intrinsic substituent effects and the influences of substitution patterns, A<sub>3</sub>-type versus A<sub>2</sub>B-type substitution
The antipodal introduction of two bromine atoms on the 2,12 β-pyrrolic position of 5,10,15,20-tetra...
Carbaporphyrins are porphyrin analogs in which one of the pyrrole units are replaced with a carbocyc...
An improved methodology is reported for the regioselective nitration of the phenyl groups of meso-te...
Rational synthesis of A<sub>2</sub>B-type <i>meso</i>-arylsubporphyrins has been accomplished by the...
The rational synthesis of meso-aryl substituted porphyrins and related macrocycles were investigated...
This paper describes the synthesis of three new porphyrins 1-3 of alternate A(2)B(2) structure, by c...
International audienceWe have developed new conditions that afford regioisomerically pure trans-A(2)...
Tripyrranes with <i>tert</i>-butyl and phenyl substituents have been prepared and used to synthesize...
5-(4-X-Phenyl)-10,15,20-tris(substituted phenyl) porphyrins (4-6) were synthesized from meso-(substi...
A simple straightforward synthesis of N<sub>3</sub>S, N<sub>2</sub>S<sub>2</sub>, N<sub>2</sub>O<sub...
Four new synthetic routes to meso-tetraarylporphyrins using a MacDonald-type 2 + 2 condensation are ...
The nucleophilic substitution of aromatic moieties (SNAr) has been known for over 150 years and foun...
The continued development of new medicinal and industrial uses of highly substituted porphyrins, esp...
The introduction of functional groups into the mesoposition of dipyrromethanes, boron-dipyrromethene...
The antipodal introduction of two bromine atoms on the 2,12 \u3b2-pyrrolic position of 5,10,15,20-te...
The antipodal introduction of two bromine atoms on the 2,12 β-pyrrolic position of 5,10,15,20-tetra...
Carbaporphyrins are porphyrin analogs in which one of the pyrrole units are replaced with a carbocyc...
An improved methodology is reported for the regioselective nitration of the phenyl groups of meso-te...
Rational synthesis of A<sub>2</sub>B-type <i>meso</i>-arylsubporphyrins has been accomplished by the...
The rational synthesis of meso-aryl substituted porphyrins and related macrocycles were investigated...
This paper describes the synthesis of three new porphyrins 1-3 of alternate A(2)B(2) structure, by c...
International audienceWe have developed new conditions that afford regioisomerically pure trans-A(2)...
Tripyrranes with <i>tert</i>-butyl and phenyl substituents have been prepared and used to synthesize...
5-(4-X-Phenyl)-10,15,20-tris(substituted phenyl) porphyrins (4-6) were synthesized from meso-(substi...
A simple straightforward synthesis of N<sub>3</sub>S, N<sub>2</sub>S<sub>2</sub>, N<sub>2</sub>O<sub...
Four new synthetic routes to meso-tetraarylporphyrins using a MacDonald-type 2 + 2 condensation are ...
The nucleophilic substitution of aromatic moieties (SNAr) has been known for over 150 years and foun...
The continued development of new medicinal and industrial uses of highly substituted porphyrins, esp...
The introduction of functional groups into the mesoposition of dipyrromethanes, boron-dipyrromethene...
The antipodal introduction of two bromine atoms on the 2,12 \u3b2-pyrrolic position of 5,10,15,20-te...
The antipodal introduction of two bromine atoms on the 2,12 β-pyrrolic position of 5,10,15,20-tetra...
Carbaporphyrins are porphyrin analogs in which one of the pyrrole units are replaced with a carbocyc...
An improved methodology is reported for the regioselective nitration of the phenyl groups of meso-te...