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Schmidt rearrangement of 1,2,3,5,10,10a‐hexahydropyrrolo[1,2‐<i>b</i>]‐isoquinoline‐3,10‐diones
12
Citations
26
References
1994
Year
EngineeringHeterocyclicSchmidt RearrangementChemical ReactivityOrganic ChemistryC Nmr SpectroscopyStereoselective SynthesisChemistryHeterocycle ChemistrySynthetic ChemistryBiomolecular Engineering
Abstract The Schmidt rearrangement of 1,2,3,5,10,10a‐hexahydropyrrolo[1,2‐ b ]isoquinoline‐3,10‐diones has been studied. The structure of the lactams obtained has been determined by chemical reactivity and characterized by means of ir, 1 H and 13 C nmr spectroscopy.
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1991 | 315 | |
1964 | 245 | |
1985 | 108 | |
1990 | 68 | |
1991 | 66 | |
A novel synthesis of L-pyroglutamic acid derivatives from L-proline : Utility of N-protecting groups for ruthenium tetroxide oxidation of cyclic .ALPHA.-amino acids. Shigeyuki Yoshifuji, Kenichi Tanaka, Tomoyuki Kawai, Chemical and Pharmaceutical Bulletin Bioorganic ChemistryEngineeringOrganic ChemistryChemistryRuthenium Tetroxide Oxidation | 1986 | 64 |
1993 | 50 | |
1991 | 50 | |
1991 | 42 | |
1989 | 39 |
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