FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W2078398963> ?p ?o ?g. }

• W2078398963 endingPage "5286" @default.
• W2078398963 startingPage "5274" @default.
• W2078398963 abstract "The O,O-acetalic compounds (RS)-3-methoxy-1-[(2)- or (4)-nitrobenzenesulfonyl)]-1,2,3,5-tetrahydro-4,1-benzoxazepine have been studied in the Lewis acid-mediated condensation with 6-chloropurine. 6-Chloropurine leads to the N-7″ aminalic bond in the cyclic products and mainly to the N-9″ aminalic bond in the acyclic ones. Substitution of the chlorine atom at the 6″ position of the purine moiety is more feasible when the ring is alkylated at N-7″ than at N-9″. Exchange with a hydroxyl group is performed with water traces in deuterated dimethylsulfoxide at room temperature in a solvent-mediated process. The exchange with strong nucleophiles (e.g., thiophenol) does not need further activation." @default.
• W2078398963 created "2016-06-24" @default.
• W2078398963 creator A5008899556 @default.
• W2078398963 creator A5009949936 @default.
• W2078398963 creator A5031177539 @default.
• W2078398963 creator A5038051629 @default.
• W2078398963 creator A5047938030 @default.
• W2078398963 creator A5091147103 @default.
• W2078398963 date "2007-06-01" @default.
• W2078398963 modified "2023-10-18" @default.
• W2078398963 title "Synthesis and reactivity of (RS)-6-chloro-7- or 9-(1,2,3,5-tetrahydro-4,1-benzoxazepin-3-yl)-7H- or 9H-purines bearing a nitrobenzenesulfonyl group on the nitrogen atom" @default.
• W2078398963 cites W1967501480 @default.
• W2078398963 cites W2002410164 @default.
• W2078398963 cites W2012513480 @default.
• W2078398963 cites W2014905489 @default.
• W2078398963 cites W2034948450 @default.
• W2078398963 cites W2040238735 @default.
• W2078398963 cites W2048331362 @default.
• W2078398963 cites W2053181269 @default.
• W2078398963 cites W2053449814 @default.
• W2078398963 cites W2054986201 @default.
• W2078398963 cites W2057943570 @default.
• W2078398963 cites W2063693099 @default.
• W2078398963 cites W2071165836 @default.
• W2078398963 cites W2071878948 @default.
• W2078398963 cites W2102686696 @default.
• W2078398963 cites W2148066840 @default.
• W2078398963 cites W2163088052 @default.
• W2078398963 cites W2320124929 @default.
• W2078398963 cites W2949228689 @default.
• W2078398963 cites W2950401935 @default.
• W2078398963 cites W2950490936 @default.
• W2078398963 cites W2951702693 @default.
• W2078398963 cites W2952893198 @default.
• W2078398963 cites W1975035708 @default.
• W2078398963 doi "https://doi.org/10.1016/j.tet.2007.03.155" @default.
• W2078398963 hasPublicationYear "2007" @default.
• W2078398963 type Work @default.
• W2078398963 sameAs 2078398963 @default.
• W2078398963 citedByCount "8" @default.
• W2078398963 countsByYear W20783989632014 @default.
• W2078398963 countsByYear W20783989632015 @default.
• W2078398963 countsByYear W20783989632017 @default.
• W2078398963 countsByYear W20783989632021 @default.
• W2078398963 crossrefType "journal-article" @default.
• W2078398963 hasAuthorship W2078398963A5008899556 @default.
• W2078398963 hasAuthorship W2078398963A5009949936 @default.
• W2078398963 hasAuthorship W2078398963A5031177539 @default.
• W2078398963 hasAuthorship W2078398963A5038051629 @default.
• W2078398963 hasAuthorship W2078398963A5047938030 @default.
• W2078398963 hasAuthorship W2078398963A5091147103 @default.
• W2078398963 hasConcept C142724271 @default.
• W2078398963 hasConcept C149635348 @default.
• W2078398963 hasConcept C155647269 @default.
• W2078398963 hasConcept C169586020 @default.
• W2078398963 hasConcept C178790620 @default.
• W2078398963 hasConcept C181199279 @default.
• W2078398963 hasConcept C185592680 @default.
• W2078398963 hasConcept C204787440 @default.
• W2078398963 hasConcept C2776910235 @default.
• W2078398963 hasConcept C2781311116 @default.
• W2078398963 hasConcept C2993420144 @default.
• W2078398963 hasConcept C41008148 @default.
• W2078398963 hasConcept C537208039 @default.
• W2078398963 hasConcept C58312451 @default.
• W2078398963 hasConcept C71240020 @default.
• W2078398963 hasConcept C71924100 @default.
• W2078398963 hasConceptScore W2078398963C142724271 @default.
• W2078398963 hasConceptScore W2078398963C149635348 @default.
• W2078398963 hasConceptScore W2078398963C155647269 @default.
• W2078398963 hasConceptScore W2078398963C169586020 @default.
• W2078398963 hasConceptScore W2078398963C178790620 @default.
• W2078398963 hasConceptScore W2078398963C181199279 @default.
• W2078398963 hasConceptScore W2078398963C185592680 @default.
• W2078398963 hasConceptScore W2078398963C204787440 @default.
• W2078398963 hasConceptScore W2078398963C2776910235 @default.
• W2078398963 hasConceptScore W2078398963C2781311116 @default.
• W2078398963 hasConceptScore W2078398963C2993420144 @default.
• W2078398963 hasConceptScore W2078398963C41008148 @default.
• W2078398963 hasConceptScore W2078398963C537208039 @default.
• W2078398963 hasConceptScore W2078398963C58312451 @default.
• W2078398963 hasConceptScore W2078398963C71240020 @default.
• W2078398963 hasConceptScore W2078398963C71924100 @default.
• W2078398963 hasIssue "24" @default.
• W2078398963 hasLocation W20783989631 @default.
• W2078398963 hasOpenAccess W2078398963 @default.
• W2078398963 hasPrimaryLocation W20783989631 @default.
• W2078398963 hasRelatedWork W1973321206 @default.
• W2078398963 hasRelatedWork W1998152715 @default.
• W2078398963 hasRelatedWork W2063193915 @default.
• W2078398963 hasRelatedWork W2073561281 @default.
• W2078398963 hasRelatedWork W2088915155 @default.
• W2078398963 hasRelatedWork W2109185572 @default.
• W2078398963 hasRelatedWork W2135119987 @default.
• W2078398963 hasRelatedWork W22828096 @default.
• W2078398963 hasRelatedWork W2338889982 @default.
• W2078398963 hasRelatedWork W2998541261 @default.
• W2078398963 hasVolume "63" @default.

• next