A facile synthesis of 3-aryl-substituted-benzothiophenes via a lewis acid mediated cyclization of 2-arylthio-acetophenones
β Scribed by Seongkon Kim; Jane Yang; Frank DiNinno
- Book ID
- 104261186
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 191 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
The boron trifluoride-etherate mediated cyclization of 2-arylthio-ketones la-h at ambient temperature gave 3-aryl-substituted benzothiophenes 2a-h in excellent yield. None of the rearranged 2-aryl-substituted benzothiophenes were observed.
π SIMILAR VOLUMES
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Titanium tetrachloride-induced cyclization of 3-(0-or m-substituted p-methoxyphenyl)-2nitro acrylates (1) provided stereoselectively (4Β’t,5~)-l-oxa-2-azaspiro[4, 5]deca-2,6,9-trien-8-ones (2). Ortho-substituted p-methoxyphenyl nitroacrylates gave 2 in good yield. 3-(4'-methoxy-l'-naphthyl)-2nitroacr