Matches in SemOpenAlex for { <https://semopenalex.org/work/W4242655402> ?p ?o ?g. }
Showing items 1 to 62 of
62
with 100 items per page.
- W4242655402 endingPage "113" @default.
- W4242655402 startingPage "105" @default.
- W4242655402 abstract "The synthesis and X-ray crystal structures of three enantiopure hydroxy-substituted amidines of the DBN-type are described. The key starting material, a 5-(phenylsulfonyl)pyrrolidin-2-one, was obtained by an oxazaborolidine-catalysed reductive desymmetrization of a meso-imide and was functionalized through N-acyliminium ion chemistry. The hydroxy groups were introduced by ozonolysis or reduction. Preliminary results on the use of the hydroxyamidines as chiral, bifunctional catalysts in selected Michael reactions are described." @default.
- W4242655402 created "2022-05-12" @default.
- W4242655402 creator A5037232926 @default.
- W4242655402 creator A5037380355 @default.
- W4242655402 creator A5038932302 @default.
- W4242655402 creator A5067503330 @default.
- W4242655402 date "2000-01-01" @default.
- W4242655402 modified "2023-09-26" @default.
- W4242655402 title "Enantioselective Synthesis of Hydroxy-Substituted DBN-Type Amidines as Potential Chiral Catalysts" @default.
- W4242655402 doi "https://doi.org/10.1002/(sici)1099-0690(200001)2000:1<105::aid-ejoc105>3.3.co;2-e" @default.
- W4242655402 hasPublicationYear "2000" @default.
- W4242655402 type Work @default.
- W4242655402 citedByCount "0" @default.
- W4242655402 crossrefType "journal-article" @default.
- W4242655402 hasAuthorship W4242655402A5037232926 @default.
- W4242655402 hasAuthorship W4242655402A5037380355 @default.
- W4242655402 hasAuthorship W4242655402A5038932302 @default.
- W4242655402 hasAuthorship W4242655402A5067503330 @default.
- W4242655402 hasConcept C145148216 @default.
- W4242655402 hasConcept C146686406 @default.
- W4242655402 hasConcept C161790260 @default.
- W4242655402 hasConcept C178790620 @default.
- W4242655402 hasConcept C185592680 @default.
- W4242655402 hasConcept C21951064 @default.
- W4242655402 hasConcept C2777190055 @default.
- W4242655402 hasConcept C2779173278 @default.
- W4242655402 hasConcept C2780443040 @default.
- W4242655402 hasConcept C30095370 @default.
- W4242655402 hasConcept C40869318 @default.
- W4242655402 hasConcept C93237805 @default.
- W4242655402 hasConceptScore W4242655402C145148216 @default.
- W4242655402 hasConceptScore W4242655402C146686406 @default.
- W4242655402 hasConceptScore W4242655402C161790260 @default.
- W4242655402 hasConceptScore W4242655402C178790620 @default.
- W4242655402 hasConceptScore W4242655402C185592680 @default.
- W4242655402 hasConceptScore W4242655402C21951064 @default.
- W4242655402 hasConceptScore W4242655402C2777190055 @default.
- W4242655402 hasConceptScore W4242655402C2779173278 @default.
- W4242655402 hasConceptScore W4242655402C2780443040 @default.
- W4242655402 hasConceptScore W4242655402C30095370 @default.
- W4242655402 hasConceptScore W4242655402C40869318 @default.
- W4242655402 hasConceptScore W4242655402C93237805 @default.
- W4242655402 hasIssue "1" @default.
- W4242655402 hasLocation W42426554021 @default.
- W4242655402 hasOpenAccess W4242655402 @default.
- W4242655402 hasPrimaryLocation W42426554021 @default.
- W4242655402 hasRelatedWork W1982446660 @default.
- W4242655402 hasRelatedWork W1990329389 @default.
- W4242655402 hasRelatedWork W2088110222 @default.
- W4242655402 hasRelatedWork W2783172341 @default.
- W4242655402 hasRelatedWork W2949868369 @default.
- W4242655402 hasRelatedWork W2950660238 @default.
- W4242655402 hasRelatedWork W2951119999 @default.
- W4242655402 hasRelatedWork W2951695403 @default.
- W4242655402 hasRelatedWork W4211167006 @default.
- W4242655402 hasRelatedWork W4242655402 @default.
- W4242655402 hasVolume "2000" @default.
- W4242655402 isParatext "false" @default.
- W4242655402 isRetracted "false" @default.
- W4242655402 workType "article" @default.