1999
DOI: 10.1016/s0040-4039(99)01893-6
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First preparation and reaction of polymer-bound 1,2-diaza-1,3-butadienes. A convenient entry to 4-triphenylphosphoranylidene-4,5-dihydropyrazol-5-ones

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Cited by 26 publications
(6 citation statements)
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“…Pyrazolin‐5‐ones, a class of important aza‐heterocycles, have exhibited a variety of applications as pharmaceutical agents,2ae synthetic scaffolds in combinatorial and medicinal chemistry,2f,g photographic couplers,2h chelating agents in coordination chemistry,2i,j and agrochemical products 2k. In particular, 4‐substituted‐pyrazolin‐5‐ones frequently set up the core frame of numerous pharmaceutically compounds,3 such as edaravone, used in inhibiting protease‐resistant prion protein accumulation 2e,4.…”
Section: Methodsmentioning
confidence: 99%
“…Pyrazolin‐5‐ones, a class of important aza‐heterocycles, have exhibited a variety of applications as pharmaceutical agents,2ae synthetic scaffolds in combinatorial and medicinal chemistry,2f,g photographic couplers,2h chelating agents in coordination chemistry,2i,j and agrochemical products 2k. In particular, 4‐substituted‐pyrazolin‐5‐ones frequently set up the core frame of numerous pharmaceutically compounds,3 such as edaravone, used in inhibiting protease‐resistant prion protein accumulation 2e,4.…”
Section: Methodsmentioning
confidence: 99%
“…Polymer-bound DD can also be prepared by using both soluble poly(ethylene glycol) (PEG) [5] or insoluble polystyrene (PS) [6][7][8] supports. The coupling sites can be both the ester group in the 4-position [5][6][7] and the azo group [8] of the azo-ene systems (Figure 1).…”
Section: Synthesis General Reactivity and Properties Of 12-diaza-1mentioning
confidence: 99%
“…The coupling sites can be both the ester group in the 4-position [5][6][7] and the azo group [8] of the azo-ene systems (Figure 1).…”
Section: Synthesis General Reactivity and Properties Of 12-diaza-1mentioning
confidence: 99%
“…A pendant NH functionality of the linear product precursor consequently effects an intramolecular cleavage of the ester linkage to create the amide vestige (PACT N−C(O)). Numerous systems of this kind are to be found for every heterocycle listed in Table 10: diketopiperazines 26 ,50a50i cyclic peptides 27 ,51a51g lactams 28 ,52a52c benzodiazepines 29 ,53 1,4‐benzodiazepine‐2,5‐diones 30 ,54a54c hydantoins 31 ,55a55m quinazoline‐2,4‐diones and pyrimidine‐2,4‐diones 32 ,56a56d pyrazolones 33 ,57a57d and 3 H ‐quinazoline‐4‐ones 34 58…”
Section: Formation Of Carboxylic Acid Derivativesmentioning
confidence: 99%