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- W2084205865 abstract "We herein described the synthesis of several 3-benzyl-2,5-diarylselenophene derivatives in moderate to good yields using (Z)-benzylselenoenynes as starting material in carbocyclization reactions. The reactions were carried out under mild conditions using only t-BuOK as base, in the complete absence of transition metals or additives. The cyclized 3-benzyl-2,5-diarylselenophenes obtained in the current protocol appear highly promising and attractive intermediates for the synthesis of polysubstituted selenophenes. For instance, 3-benzyl-2,5-diphenylselenophene was treated with Br(2) provided the corresponding 3-benzyl-4-bromo-2,5-diphenylselenophene in high yield. 4-Bromoselenophene derivative was applied as substrate in the palladium catalyzed cross-coupling reactions with boronic acids to give the Suzuki type products in excellent yields." @default.
- W2084205865 created "2016-06-24" @default.
- W2084205865 creator A5011263202 @default.
- W2084205865 creator A5020034268 @default.
- W2084205865 creator A5020412103 @default.
- W2084205865 creator A5074905169 @default.
- W2084205865 date "2011-01-01" @default.
- W2084205865 modified "2023-10-16" @default.
- W2084205865 title "Selective base-promoted synthesis of substituted selenophenes by carbocyclization of (Z)-benzylselenoenynes" @default.
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- W2084205865 doi "https://doi.org/10.1039/c0ob00844c" @default.
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- W2084205865 hasPublicationYear "2011" @default.
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