38847-62-0Relevant academic research and scientific papers
One-pot reductive conversion of nitroarenes to N-arylacetamides mediated by metallic samarium
Zhang, Yandong,Zhang, Yongmin
, p. 596 - 598 (2007/10/03)
Nitroarenes can be reduced and then converted to N-arylacetamides by metallic samarium in the presence of acetic anhydride, acetic acid and methanol in excellent yields by a one pot-procedure.
Synthesis of Substituted Dibenzophospholes. Part 5. Synthesis of Intermediates for 4- and 6-Aryl Substituents
Buttrus, Nabeel H.,Cornforth, Sir John,Hitchcock, Peter B.,Kumar, Ashok,Stuart, Alan S.
, p. 851 - 858 (2007/10/02)
6-Iodo-5-methoxy-8-methyl-1,2,3,4-tetrahydro-1,4-ethanonaphthalene was prepared from the Diels-Alder adduct of benzoquinone and cyclohexadiene.Diels-Alder condensation of 2-acetamimido-benzoquinone and 2-iodobenzoquinone (convenient, new syntheses of both quinones are described) with 2-methylcyclohexa-1,3-diene led to mixtures of adducts; the major adduct from the iodoquinone was isolated and found by X-ray analysis to have the methyl and iodo substituents at the 2- and 7-positions, respectively, of the 1,4-ethanonaphthalene skeleton.Addition of 2-acetamidobenzoquinone to mentha-2,6,8(9)-triene derived from (-)-carvone gave two regioisomers (structures determined by n.m.r. spectroscopy).In a smooth 4-step synthesis from 6,6-dimethylfulvene and benzoquinone, 6-iodo-9-syn-isopropyl-5,8-dimethoxy-1,2,3,4-tetrahydro-1,4-methanonaphthalene was prepared and its stucture confirmed by X-ray analysis.
