Novel tetrahydroquinazoline and cyclooctapyrimidine derivatives of TPP were obtained by thermal extrusion of SO2 from a porphyrin-pyrimidine fused 3-sulfolene in the presence of N-(4-nitrophenyl)maleimide.
An improvement to the synthesis of deuterated meso-tetraphenylporphyrins
β Scribed by Motoko S. Asano; Hiroshi Abe; Youkoh Kaizu
- Book ID
- 102367881
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- French
- Weight
- 146 KB
- Volume
- 49
- Category
- Article
- ISSN
- 0022-2135
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β¦ Synopsis
An improved method for the synthesis of deuterated tetraphenylporphyrins (TPPs) is reported. In this method, deuterium labelling at the pyrrole-b-position is increased to more than 95 at%. TPP is the most widely used synthetic porphyrin and high deuterium incorporation is essential for spectroscopic studies and kinetic studies involving relaxation processes.
π SIMILAR VOLUMES
The synthesis of three novel axial dinucleosides was successfully accomplished. The compounds are 5' -O, 5' -O -dithymidyl -phosphorus(V) -meso -tetraphenylporphyrin, 5' -O, 3' -O -dithymidyl -phosphorus(V) -meso -tetraphenylporphyrin, and 3' -O, 3' -O -dithymidyl -phosphorus-(V)-tetraphenylporophyr
Fused pyridinoporphyrins (3a and 3b) were obtained from the reaction of nickel (11) ~-amino-meso-tetraphenylporphyrin with propenal or methyl vinyl ketone.