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Synthesis of 5,6-dihydro-4H-thiopyran-4-ones
Authors:Jan Becher  Klaus Brsndum  Poul Hansen  Jens Peter Jan Jacobsen
Institution:Jan Becher,Klaus Brøsndum,Poul Hansen,Jens Peter Jan Jacobsen
Abstract:The anions of 1,4-diaryl-3-buten-2-ones 1 reacts with arylisothiocyanates, yielding intermediates 4 which can ring close to 5,6-dihydro-4H-thiopyran-4-ones 5 . Under similar reaction conditions ethyl 3-oxo-4-pentenoates 7 gives the 6-spiropyrans 9 . Methylation of 3 gives the S-methylated open form 6 .
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