1932
DOI: 10.1002/jlac.19324950102
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Über Phäoporphyrin a6, die Allomerisation des Chlorophylls, sowie über eine neue Methode der Einführung von Magnesium in Chlorophyll‐Derivate

Abstract: Vor kurzem haben wir fur Phaoporphyrin a8 folgende Konstitutionsformel aufgestellt welche an C,, einen Athoxylrest und eine Carbmethoxy-Gruppe, an C, den Rest des Propionsaureathylesters enthalt. Es entstand bei der Eisessig-Jodwasserstoff-Reduktion des in Athylalkohol gelosten, mit Chinon dehydrierten Athylchlorophyllids, wahrend Chlorophyllid selbst lediglich Phacporphyrin a6 (wie Formel I, statt OC,H6 an C,,:H) ergibt. Wir haben zunachst das Dehydrierungsmittel variiert durch Anwendung von Jod, wobei ebenfa… Show more

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Cited by 20 publications
(3 citation statements)
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“…Numerous porphyrins were isolated, and their constitution determined, which cannot be discussed in more detail in a short lecture. The most important among them is pheoporphyrin (11,15) (XIII) which is obtainable from the pheophorbides, also from pheophytin and chlorophyl- culty. Pheoporphyrin a3 reacts with ketone reagents and can be split by hydrolysis to chloroporphyrin e«, which is likewise a monomethyl ester and possesses the following formula (XIV):…”
Section: H3cfi-cjh6mentioning
confidence: 99%
“…Numerous porphyrins were isolated, and their constitution determined, which cannot be discussed in more detail in a short lecture. The most important among them is pheoporphyrin (11,15) (XIII) which is obtainable from the pheophorbides, also from pheophytin and chlorophyl- culty. Pheoporphyrin a3 reacts with ketone reagents and can be split by hydrolysis to chloroporphyrin e«, which is likewise a monomethyl ester and possesses the following formula (XIV):…”
Section: H3cfi-cjh6mentioning
confidence: 99%
“…Fischer also carried out allomerization experiments in alcohol, using quinone as hydrogen acceptor in place of atmospheric oxygen (66,28).…”
Section: Allomerizationmentioning
confidence: 99%
“…Fischer, on the basis of allomerization experiments with quinone in alcohol (40), assumes that the dehydrogenation takes place between the gamma and 10 positions, forming a double bond, and that the molecule may then add water or alcohol to the carbon atoms at positions 6 and 10 (1,4 addition) as is shown below.…”
Section: Journal Of Chemical Educationmentioning
confidence: 99%