A new synthesis of 4H-1-benzothiopyran-4-ones using (trimethylsilyl)methylenetriphenylphosphorane
The reaction of silyl ester of S-acyl(aroyl) thiosalicylic acids 3 with (trimethylsilyl)methylenetriphenylphosphorane 4 in step wise fashion leads to the acylphosphoranes 7, which subsequently undergo intramolecular Wittig cyclization on the thiolester carbonyl to afford the 4H-1-benzothiopyran-4-ones 8 in good to excellent yields.
Kumar, Pradeep,Bodas, Mandar S
p. 9755 - 9758
(2007/10/03)
An Efficient Approach to the Synthesis of 4H-1-Benzothiopyran-4-ones via Intramolecular Wittig Reaction
The reaction of S-acyl(aroyl)thiosalicylic acids 2 with N-phenyl(triphenylphosphoranylidene)ethenimine 3 in stepwise fashion leads to the acylphosphoranes 5 which subsequently undergo intramolecular Wittig cyclization on the thiolester carbonyl to afford
Kumar, Pradeep,Rao, Ashok T.,Pandey, Bipin
p. 1580 - 1581
(2007/10/02)
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