Formylation followed by reductive amination of 5,10,15,20-tetraphenyl porphyrin (TPP) is shown to be a versatile synthetic procedure for monosubstitution of the porphyrin core re-giospecifically at one β-position. A diverse range of substituents can be introduced in this way in good yields, including cyclen aza-crown macrocycles. © Georg Thieme Verlag Stuttgart
International audienceA versatile synthetic approach to accessing unsymmetrically substituted (trans...
Trabajo presentado en el Symposium of the Spanish Royal Society of Chemistry, celebrado en modalidad...
Synthetic studies toward the preparation of several polypyrrolic macrocycles are described. The majo...
Formylation followed by reductive amination of 5,10,15,20-tetraphenyl porphyrin (TPP) is shown to be...
New methodology has been developed for the synthesis of so-called sapphyrins, pentapyrrolic 'expande...
A convenient protocol for the preparation of 5-phenyl-10,15,20-tris(4-sulfonatophenyl)porphyrin, a w...
International audienceWe have developed new conditions that afford regioisomerically pure trans-A(2)...
The design, synthesis, and initial study of amino-functionalized porphyrins as a new class of bifunc...
Nearly all living things contain porphyrins and chlorins. They play key roles in metabolic processes...
International audienceFour free base aminoporphyrins were synthesized in two steps via regioselectiv...
An improved methodology is reported for the regioselective nitration of the phenyl groups of meso-te...
N?substitution of porphyrins has been a neglected route towards nonplanar porphyrins for the past de...
In recent years, several synthetic strategies aiming at the peripheral functionalization of porphyri...
Chapter 1 introduces the N?H?X binding motif in tetrapyrroles, which forms the basis of the research...
International audienceA versatile synthetic approach to accessing unsymmetrically substituted (trans...
Trabajo presentado en el Symposium of the Spanish Royal Society of Chemistry, celebrado en modalidad...
Synthetic studies toward the preparation of several polypyrrolic macrocycles are described. The majo...
Formylation followed by reductive amination of 5,10,15,20-tetraphenyl porphyrin (TPP) is shown to be...
New methodology has been developed for the synthesis of so-called sapphyrins, pentapyrrolic 'expande...
A convenient protocol for the preparation of 5-phenyl-10,15,20-tris(4-sulfonatophenyl)porphyrin, a w...
International audienceWe have developed new conditions that afford regioisomerically pure trans-A(2)...
The design, synthesis, and initial study of amino-functionalized porphyrins as a new class of bifunc...
Nearly all living things contain porphyrins and chlorins. They play key roles in metabolic processes...
International audienceFour free base aminoporphyrins were synthesized in two steps via regioselectiv...
An improved methodology is reported for the regioselective nitration of the phenyl groups of meso-te...
N?substitution of porphyrins has been a neglected route towards nonplanar porphyrins for the past de...
In recent years, several synthetic strategies aiming at the peripheral functionalization of porphyri...
Chapter 1 introduces the N?H?X binding motif in tetrapyrroles, which forms the basis of the research...
International audienceA versatile synthetic approach to accessing unsymmetrically substituted (trans...
Trabajo presentado en el Symposium of the Spanish Royal Society of Chemistry, celebrado en modalidad...
Synthetic studies toward the preparation of several polypyrrolic macrocycles are described. The majo...