2001
DOI: 10.1039/b108059h
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4-Phenyloxazolidin-2-ones and isoindolin-1-ones: chiral auxiliaries for Diels–Alder reactions of N-substituted 1,3-dienes

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Cited by 6 publications
(1 citation statement)
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“…Approaches in literature for isoindolinone synthesis include Heck cyclization, Diels–Alder approach, ring-closure of hydrazones, reactions of acyliminium ion, exploiting carbanion methodology, and various enantioselective approaches including our recent domino Cu­(I)-catalyzed enantioselective propargylation/lactamization and organocatalytic Mannich/lactamization sequence . On the other hand, synthesis of isoquinolines involves various diastereoselective processes , and catalytic enantioselective processes. , Although some elegant approaches to these targets have been reported, still there exist a fewer number of reports to synthesize them applying a general catalytic route.…”
mentioning
confidence: 99%
“…Approaches in literature for isoindolinone synthesis include Heck cyclization, Diels–Alder approach, ring-closure of hydrazones, reactions of acyliminium ion, exploiting carbanion methodology, and various enantioselective approaches including our recent domino Cu­(I)-catalyzed enantioselective propargylation/lactamization and organocatalytic Mannich/lactamization sequence . On the other hand, synthesis of isoquinolines involves various diastereoselective processes , and catalytic enantioselective processes. , Although some elegant approaches to these targets have been reported, still there exist a fewer number of reports to synthesize them applying a general catalytic route.…”
mentioning
confidence: 99%