Matches in SemOpenAlex for { <https://semopenalex.org/work/W2952672052> ?p ?o ?g. }
Showing items 1 to 51 of
51
with 100 items per page.
- W2952672052 abstract "Several perhydroindene derivatives were prepared from 2,7-dimethyl-1,3,7-octatriene (I) via Diels Alder reaction followed by cyclisation. For example, the Diels Alder reaction between I and methyl vinyl ketone (II) in the presence of Lewis acid afforded 4-acetyl-3-(3-methylbut-3-enyl)-1-methylcyclohexene (IIIa), which, upon treatment with phosphoric acid, was converted to a mixture of 2-acetyl-5,7,7-trimethyl-bicyclo [4,3,0]-non-1-(6)-ene (IV), 2-acetyl-5,7,7-trimethylbicyclo[4,3,0]-non-1-ene (VI) and 2-isopropyl-3,6-dimethylindene (V)." @default.
- W2952672052 created "2019-06-27" @default.
- W2952672052 creator A5010998177 @default.
- W2952672052 creator A5014038576 @default.
- W2952672052 creator A5015752456 @default.
- W2952672052 creator A5056097287 @default.
- W2952672052 date "1977-11-29" @default.
- W2952672052 modified "2023-09-23" @default.
- W2952672052 title "ChemInform Abstract: CONVENIENT SYNTHESIS OF PERHYDROINDENE DERIVATIVES FROM 2,7-DIMETHYL-1,3,7-OCTATRIENE" @default.
- W2952672052 cites W2141834941 @default.
- W2952672052 doi "https://doi.org/10.1002/chin.197748198" @default.
- W2952672052 hasPublicationYear "1977" @default.
- W2952672052 type Work @default.
- W2952672052 sameAs 2952672052 @default.
- W2952672052 citedByCount "0" @default.
- W2952672052 crossrefType "journal-article" @default.
- W2952672052 hasAuthorship W2952672052A5010998177 @default.
- W2952672052 hasAuthorship W2952672052A5014038576 @default.
- W2952672052 hasAuthorship W2952672052A5015752456 @default.
- W2952672052 hasAuthorship W2952672052A5056097287 @default.
- W2952672052 hasConcept C104264131 @default.
- W2952672052 hasConcept C155647269 @default.
- W2952672052 hasConcept C161790260 @default.
- W2952672052 hasConcept C163638829 @default.
- W2952672052 hasConcept C178790620 @default.
- W2952672052 hasConcept C185592680 @default.
- W2952672052 hasConcept C24961977 @default.
- W2952672052 hasConcept C2776622989 @default.
- W2952672052 hasConcept C2776753869 @default.
- W2952672052 hasConcept C2777738585 @default.
- W2952672052 hasConcept C27777614 @default.
- W2952672052 hasConcept C2779940776 @default.
- W2952672052 hasConceptScore W2952672052C104264131 @default.
- W2952672052 hasConceptScore W2952672052C155647269 @default.
- W2952672052 hasConceptScore W2952672052C161790260 @default.
- W2952672052 hasConceptScore W2952672052C163638829 @default.
- W2952672052 hasConceptScore W2952672052C178790620 @default.
- W2952672052 hasConceptScore W2952672052C185592680 @default.
- W2952672052 hasConceptScore W2952672052C24961977 @default.
- W2952672052 hasConceptScore W2952672052C2776622989 @default.
- W2952672052 hasConceptScore W2952672052C2776753869 @default.
- W2952672052 hasConceptScore W2952672052C2777738585 @default.
- W2952672052 hasConceptScore W2952672052C27777614 @default.
- W2952672052 hasConceptScore W2952672052C2779940776 @default.
- W2952672052 hasLocation W29526720521 @default.
- W2952672052 hasOpenAccess W2952672052 @default.
- W2952672052 hasPrimaryLocation W29526720521 @default.
- W2952672052 isParatext "false" @default.
- W2952672052 isRetracted "false" @default.
- W2952672052 magId "2952672052" @default.
- W2952672052 workType "article" @default.