1931
DOI: 10.1515/bchm2.1931.198.1-2.33
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Über Phyllobombycin und den biologischen Abbau der Chlorophylle.

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1932
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Cited by 20 publications
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“…Thus for the first time a basis was obtained for the view that the chlorophyll molecule also stood in close relation to the porphyrins; a possibility further supported by synthetic studies through conversion of blood pigment porphyrins into chlorins and rhodins (55,17,12). By bacteriological methods (19,20) chlorophyll derivatives were likewise converted into porphyrins, again a confirmation of the relations stated above. From the conversion of chlorophyll and its derivatives into phyllo-, pyrro-, and rhodo-porphyrins the presence of the porphin nucleus could not be inferred, because in view of the brutal methods of treatment involved (alcohólate breakdown at high temperature in a sealed tube) secondary synthesis might be involved; all the more since these porphyrins are poorer in carbon than the starting material.…”
Section: H3cfi-cjh6supporting
confidence: 55%
“…Thus for the first time a basis was obtained for the view that the chlorophyll molecule also stood in close relation to the porphyrins; a possibility further supported by synthetic studies through conversion of blood pigment porphyrins into chlorins and rhodins (55,17,12). By bacteriological methods (19,20) chlorophyll derivatives were likewise converted into porphyrins, again a confirmation of the relations stated above. From the conversion of chlorophyll and its derivatives into phyllo-, pyrro-, and rhodo-porphyrins the presence of the porphin nucleus could not be inferred, because in view of the brutal methods of treatment involved (alcohólate breakdown at high temperature in a sealed tube) secondary synthesis might be involved; all the more since these porphyrins are poorer in carbon than the starting material.…”
Section: H3cfi-cjh6supporting
confidence: 55%