Matches in SemOpenAlex for { <https://semopenalex.org/work/W2023394739> ?p ?o ?g. }
Showing items 1 to 59 of
59
with 100 items per page.
- W2023394739 abstract "cis and trans isomers of 1,4-dimethyl-4-nitro-1,4-dihydro-1-naphthyl acetate (1) have been isolated from a mixture of 1,4-dimethylnaphthalene and nitric acid in acetic anhydride by quenching at −40°. At room temperature only 1-methyl-4-nitromethylnaphthalene (4) is obtained. The conversion of 1,4-dimethylnaphthalene to 4 and of the cis (1a) and trans (1b) adducts to 4, by nitric acid in acetic anhydride, has been followed by n.m.r. 1,4-Dimethyl-4-nitro-1,4-dihydro-1-naphthyl nitrate (5) appears to be the immediate product from nitration of 1,4-dimethylnaphthalene in acetic anhydride, methylene chloride, or nitromethane. In acetic anhydride 5 is converted into 1. Decomposition of 1 in acetic acid gives 1,4-dimethyl-2-naphthyl acetate and some 4. The formation of 4 in this reaction is suppressed by urea." @default.
- W2023394739 created "2016-06-24" @default.
- W2023394739 creator A5025687581 @default.
- W2023394739 creator A5033435173 @default.
- W2023394739 date "1972-12-15" @default.
- W2023394739 modified "2023-09-27" @default.
- W2023394739 title "Adduct Intermediates in the Side-chain Nitration of 1,4-Dimethylnaphthalene" @default.
- W2023394739 cites W2322260641 @default.
- W2023394739 doi "https://doi.org/10.1139/v72-631" @default.
- W2023394739 hasPublicationYear "1972" @default.
- W2023394739 type Work @default.
- W2023394739 sameAs 2023394739 @default.
- W2023394739 citedByCount "16" @default.
- W2023394739 countsByYear W20233947392020 @default.
- W2023394739 crossrefType "journal-article" @default.
- W2023394739 hasAuthorship W2023394739A5025687581 @default.
- W2023394739 hasAuthorship W2023394739A5033435173 @default.
- W2023394739 hasBestOaLocation W20233947391 @default.
- W2023394739 hasConcept C108204754 @default.
- W2023394739 hasConcept C155647269 @default.
- W2023394739 hasConcept C178790620 @default.
- W2023394739 hasConcept C185592680 @default.
- W2023394739 hasConcept C204921945 @default.
- W2023394739 hasConcept C2775856698 @default.
- W2023394739 hasConcept C521977710 @default.
- W2023394739 hasConceptScore W2023394739C108204754 @default.
- W2023394739 hasConceptScore W2023394739C155647269 @default.
- W2023394739 hasConceptScore W2023394739C178790620 @default.
- W2023394739 hasConceptScore W2023394739C185592680 @default.
- W2023394739 hasConceptScore W2023394739C204921945 @default.
- W2023394739 hasConceptScore W2023394739C2775856698 @default.
- W2023394739 hasConceptScore W2023394739C521977710 @default.
- W2023394739 hasLocation W20233947391 @default.
- W2023394739 hasOpenAccess W2023394739 @default.
- W2023394739 hasPrimaryLocation W20233947391 @default.
- W2023394739 hasRelatedWork W1983305594 @default.
- W2023394739 hasRelatedWork W2000302588 @default.
- W2023394739 hasRelatedWork W2029389262 @default.
- W2023394739 hasRelatedWork W2050967016 @default.
- W2023394739 hasRelatedWork W2051056054 @default.
- W2023394739 hasRelatedWork W2057783452 @default.
- W2023394739 hasRelatedWork W2061545694 @default.
- W2023394739 hasRelatedWork W2064464621 @default.
- W2023394739 hasRelatedWork W2085367394 @default.
- W2023394739 hasRelatedWork W2086234186 @default.
- W2023394739 hasRelatedWork W2089180211 @default.
- W2023394739 hasRelatedWork W2164374899 @default.
- W2023394739 hasRelatedWork W2166648653 @default.
- W2023394739 hasRelatedWork W2343034058 @default.
- W2023394739 hasRelatedWork W2912731741 @default.
- W2023394739 hasRelatedWork W2949517672 @default.
- W2023394739 hasRelatedWork W2951269404 @default.
- W2023394739 hasRelatedWork W2951838778 @default.
- W2023394739 hasRelatedWork W2951950807 @default.
- W2023394739 hasRelatedWork W3000511350 @default.
- W2023394739 isParatext "false" @default.
- W2023394739 isRetracted "false" @default.
- W2023394739 magId "2023394739" @default.
- W2023394739 workType "article" @default.