1937
DOI: 10.1021/cr60065a002
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Chlorophyll.

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Cited by 42 publications
(22 citation statements)
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“…Interestingly, a high reactivity was observed for 2 d as compared to that of 2 a: the condensation can be performed at room temperature, and the desired pyrrolyldipyrromethenes 1 i-k were obtained in 72-79 % yields upon isolation. [22] In our case, the acid-catalyzed condensation of 5-halo-2-formylpyrroles (or isoindoles) with an a-unsubstituted pyrrole generated the 9-halodipyrromethene A in salt form (Scheme 2). The acid-catalyzed condensation of a 2-formylpyrrole with an a-unsubstituted pyrrole is known to form dipyrromethenes in a salt form [21] before subsequent workup with base.…”
mentioning
confidence: 79%
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“…Interestingly, a high reactivity was observed for 2 d as compared to that of 2 a: the condensation can be performed at room temperature, and the desired pyrrolyldipyrromethenes 1 i-k were obtained in 72-79 % yields upon isolation. [22] In our case, the acid-catalyzed condensation of 5-halo-2-formylpyrroles (or isoindoles) with an a-unsubstituted pyrrole generated the 9-halodipyrromethene A in salt form (Scheme 2). The acid-catalyzed condensation of a 2-formylpyrrole with an a-unsubstituted pyrrole is known to form dipyrromethenes in a salt form [21] before subsequent workup with base.…”
mentioning
confidence: 79%
“…Since their initial synthesis, by Hans Fischer in 1934, dipyrromethenes as dipyrrinato ligands have been widely studied and continually attract interest because of their synthetic utility as porphyrin precursors and their rich photophysical properties. [22] In our case, the acid-catalyzed condensation of 5-halo-2-formylpyrroles (or isoindoles) with an a-unsubstituted pyrrole generated the 9-halodipyrromethene A in salt form (Scheme 2). Subsequently, the proton-ated azafulvene unit in this in situ generated A could participate in an unexpected S N Ar reaction with a suitable a-unsubstituted pyrrole to form the pyrroledipyrromethene B.…”
mentioning
confidence: 79%
“…While Chl a features a methyl group in that position, Chl b is oxidized to an aldehyde group. The structural identification of chlorophylls was first described by Hans Fischer ( Fischer 1937 ; Woodward 1960 ), while the corresponding nomenclature was later updated in accordance with IUPAC rules ( Merritt and Loening 1980 ) (see Supplementary Figure S1 ). Specifically, Chl a is part of the photosynthetic pigment-protein reaction center in all oxygenic photoautotrophs.…”
Section: Introductionmentioning
confidence: 99%
“…It accumulates in the blood when plant-or mycotoxin-induced liver damage prevents its normal biliary excretion. Here, the name phytoporphyrin, proposed by the International Union of Pure and Applied Chemistry and International Union of Biochemistry Joint Commission on Biochemical Nomenclature (Moss 1987), is preferred over the old name of phylloerythrin (Fischer 1937).…”
Section: Introduction and Overview Of Photosensitisation And The Dermentioning
confidence: 99%