New route to protoporphyrins III and XIII from common starting pyrroles
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference14 articles.
1. Electrochemistry of monoazahemin reconstituted myoglobin at an indium oxide electrode
2. Mie, Y.; Sonoda, K.; Imamura; A.; Kishita, M.; Neya, S.; Funasaki, N.; Taniguchi, I. Bioelectrochemistry, submitted.
3. Electroanalytical chemistry of myoglobin with modification of distal histidine by cyanated imidazole
4. Effect of rapid heme rotation on electrochemistry of myoglobin
5. Electrochemical and spectroelectrochemical properties of manganese reconstituted myoglobin
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1. Synthesis of 1,4,5,8-tetraethyl-2,3,6,7-tetravinylporphyrin from a Knorr's pyrrole analogue;Tetrahedron;2017-11
2. Synthesis of type III isomers of diacetyldeutero-, hemato-, and protoporphyrins with the use of Knorr's pyrrole;Tetrahedron;2016-07
3. Electrochemistry of Biologically Related Metal Complexes and Its Applications;Bulletin of Japan Society of Coordination Chemistry;2010
4. A Dehydrohalogenation Methodology for Synthesizing Terminal Olefins under Mild Conditions;Synthesis;2006-08-21
5. Synthesis of formyl-thienylpyrroles: versatile building blocks for NLO materials;Tetrahedron;2006-04
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