Matches in SemOpenAlex for { <https://semopenalex.org/work/W939959932> ?p ?o ?g. }
Showing items 1 to 60 of
60
with 100 items per page.
- W939959932 endingPage "361" @default.
- W939959932 startingPage "351" @default.
- W939959932 abstract "Publisher Summary The chapter presents procedures for the synthesis of the Δ3 and Δ4-compounds. The sodium borohydride reduction of triazolium compounds5 and the vinyl azide additions to triazolinediones6 appear most promising for the formation of Δ3-triazolines. The preparation of Δ4-1,2,3-Triazolines involves the reaction of diazonium compounds of primary aromatic or heterocyclic mono- or diamines at pH 8–12 with inorganic acid esters of diethanolamines.2 When dialkylamines are used in place of the esters, l-alkyl-A4-triazolines are obtained. Both Δ3- and Δ4-1,2,3-triazolines have the 1H-structure. The ultraviolet spectrum of Δ4-1,2,3-triazoline-4,5-dicarboxylate is recorded. The infrared spectrum establishes the presence or absence of the NH function in the Δ3- and Δ4-triazolines; in the NH absorption appears at 3300 cm-1. They do not suffer nitrogen loss in the mass spectrum, and molecular ion peaks are reported for several related bicyclic Δ3-1,2,3-triazolines. The chemistry of Δ3- and Δ4-1,2,3-triazolines is still in its beginnings and few reactions are reported." @default.
- W939959932 created "2016-06-24" @default.
- W939959932 creator A5019440974 @default.
- W939959932 date "1984-01-01" @default.
- W939959932 modified "2023-10-16" @default.
- W939959932 title "Δ3- and δ4-1,2,3-Triazolines" @default.
- W939959932 cites W1968052362 @default.
- W939959932 cites W1971918716 @default.
- W939959932 cites W1981545477 @default.
- W939959932 cites W1995533239 @default.
- W939959932 cites W2006644677 @default.
- W939959932 cites W2012551124 @default.
- W939959932 cites W2028659411 @default.
- W939959932 cites W2033072585 @default.
- W939959932 cites W2038119027 @default.
- W939959932 cites W2039494850 @default.
- W939959932 cites W2053158318 @default.
- W939959932 cites W2054405594 @default.
- W939959932 cites W2059388327 @default.
- W939959932 cites W2084245075 @default.
- W939959932 cites W2085667146 @default.
- W939959932 cites W2134483526 @default.
- W939959932 cites W2168976021 @default.
- W939959932 cites W2208434346 @default.
- W939959932 cites W2312896379 @default.
- W939959932 cites W2322972755 @default.
- W939959932 cites W2335360666 @default.
- W939959932 cites W2952516341 @default.
- W939959932 cites W3024284890 @default.
- W939959932 cites W4249870343 @default.
- W939959932 cites W79270063 @default.
- W939959932 doi "https://doi.org/10.1016/s0065-2725(08)60244-5" @default.
- W939959932 hasPublicationYear "1984" @default.
- W939959932 type Work @default.
- W939959932 sameAs 939959932 @default.
- W939959932 citedByCount "5" @default.
- W939959932 countsByYear W9399599322019 @default.
- W939959932 crossrefType "book-chapter" @default.
- W939959932 hasAuthorship W939959932A5019440974 @default.
- W939959932 hasConcept C192562407 @default.
- W939959932 hasConceptScore W939959932C192562407 @default.
- W939959932 hasLocation W9399599321 @default.
- W939959932 hasOpenAccess W939959932 @default.
- W939959932 hasPrimaryLocation W9399599321 @default.
- W939959932 hasRelatedWork W2018879842 @default.
- W939959932 hasRelatedWork W2325423348 @default.
- W939959932 hasRelatedWork W2737498735 @default.
- W939959932 hasRelatedWork W2744391499 @default.
- W939959932 hasRelatedWork W2898370298 @default.
- W939959932 hasRelatedWork W2899084033 @default.
- W939959932 hasRelatedWork W3041790586 @default.
- W939959932 hasRelatedWork W3120461830 @default.
- W939959932 hasRelatedWork W3144504424 @default.
- W939959932 hasRelatedWork W4292492973 @default.
- W939959932 isParatext "false" @default.
- W939959932 isRetracted "false" @default.
- W939959932 magId "939959932" @default.
- W939959932 workType "book-chapter" @default.