Matches in SemOpenAlex for { <https://semopenalex.org/work/W1896102018> ?p ?o ?g. }
Showing items 1 to 62 of
62
with 100 items per page.
- W1896102018 endingPage "2464" @default.
- W1896102018 startingPage "2460" @default.
- W1896102018 abstract "Several methods of eliminative cyclisations of diastereoisomeric disecondary 1,4-diols and their 1,4-disulphonate esters, leading to the formation of tetrahydrofurans, have been studied, and it was found that they all proceed stereoselectively by SN2-type mechanisms, with inversion of configuration at one (1,4-diols) or both (1,4-disul-phonates) chiral centres, so that meso(i.e. erythro) 1,4-diols and ±(i.e. threo) 1,4-dimesylates afford only trans-2,5-dialkyl-tetrahydrofurans, while the respective diastereoisomeric substrates are converted exclusively into cis-2,5-dialkyltetrahydrofurans." @default.
- W1896102018 created "2016-06-24" @default.
- W1896102018 creator A5009768462 @default.
- W1896102018 creator A5030927421 @default.
- W1896102018 creator A5067009099 @default.
- W1896102018 date "1972-01-01" @default.
- W1896102018 modified "2023-10-01" @default.
- W1896102018 title "Stereochemistry of cyclic ether formation. Part I. Stereoselective intramolecular cyclisation of aliphatic disecondary 1,4-diols and their sulphonate esters to tetrahydrofurans" @default.
- W1896102018 doi "https://doi.org/10.1039/p19720002460" @default.
- W1896102018 hasPublicationYear "1972" @default.
- W1896102018 type Work @default.
- W1896102018 sameAs 1896102018 @default.
- W1896102018 citedByCount "22" @default.
- W1896102018 countsByYear W18961020182012 @default.
- W1896102018 countsByYear W18961020182014 @default.
- W1896102018 countsByYear W18961020182016 @default.
- W1896102018 countsByYear W18961020182017 @default.
- W1896102018 countsByYear W18961020182019 @default.
- W1896102018 countsByYear W18961020182020 @default.
- W1896102018 countsByYear W18961020182021 @default.
- W1896102018 crossrefType "journal-article" @default.
- W1896102018 hasAuthorship W1896102018A5009768462 @default.
- W1896102018 hasAuthorship W1896102018A5030927421 @default.
- W1896102018 hasAuthorship W1896102018A5067009099 @default.
- W1896102018 hasConcept C138716334 @default.
- W1896102018 hasConcept C161790260 @default.
- W1896102018 hasConcept C178790620 @default.
- W1896102018 hasConcept C181647583 @default.
- W1896102018 hasConcept C185592680 @default.
- W1896102018 hasConcept C2780407432 @default.
- W1896102018 hasConcept C71240020 @default.
- W1896102018 hasConcept C75079739 @default.
- W1896102018 hasConcept C96765332 @default.
- W1896102018 hasConceptScore W1896102018C138716334 @default.
- W1896102018 hasConceptScore W1896102018C161790260 @default.
- W1896102018 hasConceptScore W1896102018C178790620 @default.
- W1896102018 hasConceptScore W1896102018C181647583 @default.
- W1896102018 hasConceptScore W1896102018C185592680 @default.
- W1896102018 hasConceptScore W1896102018C2780407432 @default.
- W1896102018 hasConceptScore W1896102018C71240020 @default.
- W1896102018 hasConceptScore W1896102018C75079739 @default.
- W1896102018 hasConceptScore W1896102018C96765332 @default.
- W1896102018 hasIssue "0" @default.
- W1896102018 hasLocation W18961020181 @default.
- W1896102018 hasOpenAccess W1896102018 @default.
- W1896102018 hasPrimaryLocation W18961020181 @default.
- W1896102018 hasRelatedWork W1981358338 @default.
- W1896102018 hasRelatedWork W2060086256 @default.
- W1896102018 hasRelatedWork W2086191285 @default.
- W1896102018 hasRelatedWork W2089894343 @default.
- W1896102018 hasRelatedWork W2093846312 @default.
- W1896102018 hasRelatedWork W2400736630 @default.
- W1896102018 hasRelatedWork W2802651363 @default.
- W1896102018 hasRelatedWork W2952008709 @default.
- W1896102018 hasRelatedWork W2966059910 @default.
- W1896102018 hasRelatedWork W989071899 @default.
- W1896102018 isParatext "false" @default.
- W1896102018 isRetracted "false" @default.
- W1896102018 magId "1896102018" @default.
- W1896102018 workType "article" @default.