3 article(s) from Ábrányi-Balogh, Péter
Rearrangement of methylenedioxy-substituted aminoaldehyde 1a to regioisomer 2a and formation of the...
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Synthesis of 1-arylisoindoles 6 and formation of dimers 5.
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Rearrangement of aminoaldehydes 1 to regioisomers 2 and formation of dimer-like products 3 and 8.
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X-ray structures of compounds 3b (left) and 8b (right).
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Proposed mechanism of the isomerization of aldehydes 1 via isoindoles 4.
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Proposed mechanism of the formation of dimer-like products 3a,b.
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Proposed mechanism for the formation of dimer-like products 8a,b.
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Dimerization of indole under acidic conditions.
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Gibbs free energy diagram for the 1→2 rearrangement.
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Reaction of o-(pivaloylaminomethyl)benzaldehyde (1e) to give dimer-like products 23a and 23b.
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X-ray structures of compounds 23a (left) and 23b (right).
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Structures of the minimal energy conformer of stereoisomer 23a and those of two minimal energy conf...
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Beilstein J. Org. Chem. 2020, 16, 1636–1648, doi:10.3762/bjoc.16.136
Synthetic routes to O-thiocarbamates and dithiocarbamates.
Substrate scope of isocyanides. aReaction conditions: 1 (1 mmol), S8 (2 mmol), 2a (2mmol), NaH (2 m...
Substrate scope of alcohols. Reaction conditions: 1a (1 mmol), S8 (2 mmol), 2 (2mmol), NaH (2 mmol)...
Substrate scope of thiols. Reaction conditions: 1a (1 mmol), S8 (1.2 mmol), 4 (2 mmol), NaOH (2 mmo...
Scaled-up synthesis for 3a.
Multicomponent domino synthesis of quinazolinone 7.
Beilstein J. Org. Chem. 2019, 15, 1523–1533, doi:10.3762/bjoc.15.155
Synthesis of starting N-benzylideneamines 1.
Addition of diethyl phosphite to N-benzylidene(butyl)amine in acetonitrile.
IR spectra of the reaction components in acetonitrile solution.
A segment of the time-dependent IR spectrum for the addition of diethyl phosphite to N-benzylidene(...
Concentration profiles of the reaction components in the addition reaction at 80 °C in acetonitrile....
Atomic numbering with anisotropic displacements plot of 5b at −100 °C.
Atomic numbering with anisotropic displacements plot of 5d at −100 °C.
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The energy diagram for the reaction with dimethyl phosphite.
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The energy diagram for the reaction with diphenylphosphine oxide.
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Beilstein J. Org. Chem. 2017, 13, 76–86, doi:10.3762/bjoc.13.10
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