Synthesis of vertical‐type bis(pyridodipyrimidines) as a redox catalyst and their autorecycling oxidation of alcohols | Zendy

Yamato Hirotake | Zendy; Nagamatsu Tomohisa | Zendy; Yoneda Fumio | Zendy

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Synthesis of vertical‐type bis(pyridodipyrimidines) as a redox catalyst and their autorecycling oxidation of alcohols

Author(s) -

Yamato Hirotake,

Nagamatsu Tomohisa,

Yoneda Fumio

Publication year - 1991

Publication title -

journal of heterocyclic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.321

H-Index - 59

eISSN - 1943-5193

pISSN - 0022-152X

DOI - 10.1002/jhet.5570280509

Subject(s) - chemistry , redox , acetic acid , catalysis , condensation , alcohol oxidation , medicinal chemistry , organic chemistry , menthol , physics , thermodynamics

Condensation of bis(3‐methyluracil‐6‐ylamino)alkanes with 6‐chloro‐5‐formyl‐3‐methyluracil or 2,4,6‐trichloropyrimidine‐5‐carbaldehyde in acetic acid gave the respective bis(pyridodipyrimidin‐10‐yl)alkanes (vertical‐type bis(pyridodipyrimidines)). The vertical‐type bis(pyridodipyrimidines) exhibited autorecycling turnover oxidation toward cyclopentanol and l ‐menthol to give the corresponding carbonyl compounds.

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