Matches in SemOpenAlex for { <https://semopenalex.org/work/W46231330> ?p ?o ?g. }
Showing items 1 to 61 of
61
with 100 items per page.
- W46231330 endingPage "183" @default.
- W46231330 startingPage "177" @default.
- W46231330 abstract "Abstract Coupling of alkylamines to cyanogen bromide-activated agarose results in the formation of N-substituted isoureas, which are good nucleophiles. The nucleophilic attack of these isoureas on the active chromogenic ester p-nitrophenyl acetate causes the release of an equivalent amount of p-nitrophenolate. This constitutes the basis for a direct determination of alkylamino groups in substituted agaroses." @default.
- W46231330 created "2016-06-24" @default.
- W46231330 creator A5027260843 @default.
- W46231330 date "1976-11-01" @default.
- W46231330 modified "2023-09-23" @default.
- W46231330 title "Nucleophilicity of isourea linkages in substituted agaroses" @default.
- W46231330 cites W1484115349 @default.
- W46231330 cites W1896219625 @default.
- W46231330 cites W1969709058 @default.
- W46231330 cites W1975655883 @default.
- W46231330 cites W1987065128 @default.
- W46231330 cites W1991473002 @default.
- W46231330 cites W2048923862 @default.
- W46231330 cites W2061636222 @default.
- W46231330 cites W2086765626 @default.
- W46231330 cites W2089345726 @default.
- W46231330 cites W2325111119 @default.
- W46231330 cites W4247802037 @default.
- W46231330 doi "https://doi.org/10.1016/0003-2697(76)90276-1" @default.
- W46231330 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/998963" @default.
- W46231330 hasPublicationYear "1976" @default.
- W46231330 type Work @default.
- W46231330 sameAs 46231330 @default.
- W46231330 citedByCount "12" @default.
- W46231330 countsByYear W462313302014 @default.
- W46231330 countsByYear W462313302015 @default.
- W46231330 countsByYear W462313302018 @default.
- W46231330 countsByYear W462313302021 @default.
- W46231330 countsByYear W462313302022 @default.
- W46231330 crossrefType "journal-article" @default.
- W46231330 hasAuthorship W46231330A5027260843 @default.
- W46231330 hasConcept C161790260 @default.
- W46231330 hasConcept C178907741 @default.
- W46231330 hasConcept C185592680 @default.
- W46231330 hasConcept C55493867 @default.
- W46231330 hasConceptScore W46231330C161790260 @default.
- W46231330 hasConceptScore W46231330C178907741 @default.
- W46231330 hasConceptScore W46231330C185592680 @default.
- W46231330 hasConceptScore W46231330C55493867 @default.
- W46231330 hasIssue "1" @default.
- W46231330 hasLocation W462313301 @default.
- W46231330 hasLocation W462313302 @default.
- W46231330 hasOpenAccess W46231330 @default.
- W46231330 hasPrimaryLocation W462313301 @default.
- W46231330 hasRelatedWork W1993926701 @default.
- W46231330 hasRelatedWork W2021939235 @default.
- W46231330 hasRelatedWork W2055791862 @default.
- W46231330 hasRelatedWork W2059767860 @default.
- W46231330 hasRelatedWork W2090776755 @default.
- W46231330 hasRelatedWork W2127336791 @default.
- W46231330 hasRelatedWork W2341954738 @default.
- W46231330 hasRelatedWork W2949233043 @default.
- W46231330 hasRelatedWork W2952071652 @default.
- W46231330 hasRelatedWork W2953319580 @default.
- W46231330 hasVolume "76" @default.
- W46231330 isParatext "false" @default.
- W46231330 isRetracted "false" @default.
- W46231330 magId "46231330" @default.
- W46231330 workType "article" @default.