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Structure Elucidation of the Oxidation Products of 2‐Arylidene‐1‐indanones and 2‐Arylidene‐1‐benzosuberones
Author(s) -
Tóth Gábor,
Halász Judit,
Boros Sándor,
Lévai Albert,
Nemes Csaba,
Patonay Tamás
Publication year - 1996
Publication title -
magnetic resonance in chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.483
H-Index - 72
eISSN - 1097-458X
pISSN - 0749-1581
DOI - 10.1002/(sici)1097-458x(199611)34:11<932::aid-omr978>3.0.co;2-3
Subject(s) - dimethyldioxirane , chemistry , peroxide , organic chemistry , stereochemistry , carbon 13 nmr , proton nmr
The relative configuration and stereochemistry of spiroepoxides prepared by dimethyldioxirane, alkaline hydro‐gen peroxide and m ‐chloroperoxybenzoic acid and of dione by‐products were elucidated by various 1 H and 13 C NMR methods.