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Beilstein J. Org. Chem. 2020, 16, 1111–1123, doi:10.3762/bjoc.16.98
Graphical Abstract
Figure 1: (a) General scheme for truxillic acid derivatives; (b) general scheme for symmetric 1,3-diaminotrux...
Figure 2: (a) (Z)-4-Arylidene-2-aryl-5(4H)-oxazolones used for the synthesis of 1,3-diaminotruxillic derivati...
Figure 3: (Z)-4-Arylidene-2((E)-styryl)-5(4H)-oxazolones 2a–j used in this work and overall reaction scheme.
Figure 4: Molecular drawing of the oxazolone 2c.
Scheme 1: Ortho-palladation of oxazolones 2 by treatment with Pd(OAc)2 and different structures obtained for ...
Scheme 2: [2 + 2] Photocycloaddition of cyclopalladated complexes 3 in solution to give the dinuclear cyclobu...
Figure 5: Molecular drawing of cyclobutane ortho-palladated 4a. Ellipsoids are shown at the 50% probability l...
Scheme 3: Release of the 1,3-diaminotruxillic bis-amino ester derivatives 5 by methoxycarbonylation of the Pd...
Beilstein J. Org. Chem. 2012, 8, 1569–1575, doi:10.3762/bjoc.8.179
Scheme 1: Synthesis of methyl (1H)-isoindolin-1-one-3-carboxylates by carbonylation of phenylglycine derivati...
Scheme 2: Synthesis and NMR characterization of orthometallated complex 3.
Scheme 3: Carbonylation of 1 to afford glutamate and glutamine derivatives 2a–j.
Figure 1: Scope of the carbonylation reaction.
Scheme 4: Reaction of 1 and CO in CH2Cl2 [18].
Scheme 5: Reactivity of 3 with CO in the presence (left) and absence (right) of nucleophiles.