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Paradisi et al., 2002 - Google Patents

Enantioselective synthesis of 2, 6-diaminopimelic acid derivatives. Part 3

Paradisi et al., 2002

Document ID
9065208245668479417
Author
Paradisi F
Piccinelli F
Porzi G
Sandri S
Publication year
Publication venue
Tetrahedron: Asymmetry

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Enantiomerically pure 2, 6-diaminopimelic acid derivatives 9a–c and 10a–c have been synthesized starting from the glycine-derived chiral synthon (1′ S, 1 ″S)-1. The absolute configuration of stereocenters introduced on 2 and 3 were assigned on the basis of 1H NMR …
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    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/10Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
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    • C07D207/08Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon radicals, substituted by hetero atoms, attached to ring carbon atoms
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    • C07D233/66Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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