0000000000600609

AUTHOR

Kristóf Bozó

showing 2 related works from this author

Traceless chirality transfer from a norbornene β-amino acid to pyrimido[2,1-a]isoindole enantiomers

2017

The synthesis of two enantiomeric pairs of pyrimidoisoindoles 9a, 9b and 10a, 10b is reported. During a domino ring-closure reaction, followed by cycloreversion, the chirality of diendo-(−)-(1R,2S,3R,4S)-3-aminobicyclo[2.2.1]hept-5-ene-2-carboxamide [(−)-1] was successfully transfered to heterocycles (+)-9a, (+)-10a, (−)-9b, (−)-10b and (−)-10c. peerReviewed

heterocyclesfarmasiakemiaaminohapotbiologia
researchProduct

Traceless chirality transfer from a norbornene β-amino acid to pyrimido[2,1-a]isoindole enantiomers

2017

Abstract The synthesis of two enantiomeric pairs of pyrimidoisoindoles 9a, 9b and 10a, 10b is reported. During a domino ring-closure reaction, followed by cycloreversion, the chirality of diendo-(−)-(1R,2S,3R,4S)-3-aminobicyclo[2.2.1]hept-5-ene-2-carboxamide [(−)-1] was successfully transfered to heterocycles (+)-9a, (+)-10a, (−)-9b, (−)-10b and (−)-10c.

chemistry.chemical_classificationpharmacyamino acidsheterocycles010405 organic chemistryStereochemistrybiologyOrganic Chemistry010402 general chemistrychemistry01 natural sciencesCatalysis0104 chemical sciencesAmino acidInorganic Chemistrychemistry.chemical_compoundchemistryPhysical and Theoretical ChemistryEnantiomerIsoindoleChirality (chemistry)ta116NorborneneTetrahedron: Asymmetry
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