Matches in SemOpenAlex for { <https://semopenalex.org/work/W2949402898> ?p ?o ?g. }
- W2949402898 endingPage "6732" @default.
- W2949402898 startingPage "6724" @default.
- W2949402898 abstract "The reaction of 1,2-diaza-1,3-butadienes with dialkyl phenylphosphonites under solvent-free conditions proceeds via zwitterionic intermediate and gives, by precipitation, the stable ylidic α-phosphanylidene-hydrazones that, in turn, can be transformed into the corresponding 3-phenyl-2H-1,2,3λ5-diazaphospholes. The latter compounds are converted by hydrolytic cleavage in methanol–water (95:5) into E-hydrazonophosphonates that are useful for the preparation of the corresponding β-ketophosphonates and 4-[alkoxy(phenyl)phosphoryl]-1,2-diaza-1,3-butadienes. These peculiar 1,2-diaza-1,3-butadienes, bearing an alkoxy(phenyl)phosphoryl group on the carbon atom in position 4 are also able to add different nucleophiles, such as methanol or thiourea, giving 2-[alkoxy(phenyl)phosphoryl]-2-methoxyhydrazones and 5-phosphinate-substituted thiazol-4-ones, respectively." @default.
- W2949402898 created "2019-06-27" @default.
- W2949402898 creator A5014940329 @default.
- W2949402898 creator A5018900411 @default.
- W2949402898 creator A5023770342 @default.
- W2949402898 creator A5062863201 @default.
- W2949402898 creator A5074448564 @default.
- W2949402898 creator A5078293209 @default.
- W2949402898 date "2008-07-01" @default.
- W2949402898 modified "2023-09-23" @default.
- W2949402898 title "Carbon–phosphorus bond formation and transformation in the reaction of 1,2-diaza-1,3-butadienes with alkyl phenylphosphonites" @default.
- W2949402898 cites W1575490333 @default.
- W2949402898 cites W1968479888 @default.
- W2949402898 cites W1970763130 @default.
- W2949402898 cites W1991267595 @default.
- W2949402898 cites W1992324843 @default.
- W2949402898 cites W1998312990 @default.
- W2949402898 cites W2002658085 @default.
- W2949402898 cites W2015386255 @default.
- W2949402898 cites W2019679383 @default.
- W2949402898 cites W2024798214 @default.
- W2949402898 cites W2027033941 @default.
- W2949402898 cites W2034672551 @default.
- W2949402898 cites W2053062963 @default.
- W2949402898 cites W2055338782 @default.
- W2949402898 cites W2062564470 @default.
- W2949402898 cites W2078319640 @default.
- W2949402898 cites W2079461522 @default.
- W2949402898 cites W2105572648 @default.
- W2949402898 cites W2109252541 @default.
- W2949402898 cites W2127297563 @default.
- W2949402898 cites W2154127625 @default.
- W2949402898 cites W2158730144 @default.
- W2949402898 cites W2226080102 @default.
- W2949402898 cites W2318090527 @default.
- W2949402898 cites W2949219288 @default.
- W2949402898 cites W2949408838 @default.
- W2949402898 cites W2950032065 @default.
- W2949402898 cites W2950165318 @default.
- W2949402898 cites W2950742504 @default.
- W2949402898 cites W2950745345 @default.
- W2949402898 cites W2950779512 @default.
- W2949402898 cites W2952842787 @default.
- W2949402898 cites W4233339180 @default.
- W2949402898 cites W2952267118 @default.
- W2949402898 doi "https://doi.org/10.1016/j.tet.2008.05.007" @default.
- W2949402898 hasPublicationYear "2008" @default.
- W2949402898 type Work @default.
- W2949402898 sameAs 2949402898 @default.
- W2949402898 citedByCount "8" @default.
- W2949402898 countsByYear W29494028982014 @default.
- W2949402898 countsByYear W29494028982023 @default.
- W2949402898 crossrefType "journal-article" @default.
- W2949402898 hasAuthorship W2949402898A5014940329 @default.
- W2949402898 hasAuthorship W2949402898A5018900411 @default.
- W2949402898 hasAuthorship W2949402898A5023770342 @default.
- W2949402898 hasAuthorship W2949402898A5062863201 @default.
- W2949402898 hasAuthorship W2949402898A5074448564 @default.
- W2949402898 hasAuthorship W2949402898A5078293209 @default.
- W2949402898 hasConcept C127413603 @default.
- W2949402898 hasConcept C155647269 @default.
- W2949402898 hasConcept C161790260 @default.
- W2949402898 hasConcept C175156509 @default.
- W2949402898 hasConcept C178790620 @default.
- W2949402898 hasConcept C178907741 @default.
- W2949402898 hasConcept C185592680 @default.
- W2949402898 hasConcept C187320778 @default.
- W2949402898 hasConcept C205474432 @default.
- W2949402898 hasConcept C2779607525 @default.
- W2949402898 hasConcept C2780263894 @default.
- W2949402898 hasConcept C2780538656 @default.
- W2949402898 hasConcept C2780645613 @default.
- W2949402898 hasConcept C2993252241 @default.
- W2949402898 hasConcept C3044715 @default.
- W2949402898 hasConcept C43369102 @default.
- W2949402898 hasConcept C90150868 @default.
- W2949402898 hasConcept C94412978 @default.
- W2949402898 hasConceptScore W2949402898C127413603 @default.
- W2949402898 hasConceptScore W2949402898C155647269 @default.
- W2949402898 hasConceptScore W2949402898C161790260 @default.
- W2949402898 hasConceptScore W2949402898C175156509 @default.
- W2949402898 hasConceptScore W2949402898C178790620 @default.
- W2949402898 hasConceptScore W2949402898C178907741 @default.
- W2949402898 hasConceptScore W2949402898C185592680 @default.
- W2949402898 hasConceptScore W2949402898C187320778 @default.
- W2949402898 hasConceptScore W2949402898C205474432 @default.
- W2949402898 hasConceptScore W2949402898C2779607525 @default.
- W2949402898 hasConceptScore W2949402898C2780263894 @default.
- W2949402898 hasConceptScore W2949402898C2780538656 @default.
- W2949402898 hasConceptScore W2949402898C2780645613 @default.
- W2949402898 hasConceptScore W2949402898C2993252241 @default.
- W2949402898 hasConceptScore W2949402898C3044715 @default.
- W2949402898 hasConceptScore W2949402898C43369102 @default.
- W2949402898 hasConceptScore W2949402898C90150868 @default.
- W2949402898 hasConceptScore W2949402898C94412978 @default.
- W2949402898 hasIssue "28" @default.
- W2949402898 hasLocation W29494028981 @default.
- W2949402898 hasOpenAccess W2949402898 @default.