2-Methyl-1-(methylsulfinyl)naphtho[2,1-b]furan
✍ Scribed by Choi, Hong Dae ;Woo, Hyun Mi ;Seo, Pil Ja ;Son, Byeng Wha ;Lee, Uk
- Publisher
- International Union of Crystallography
- Year
- 2006
- Tongue
- English
- Weight
- 157 KB
- Volume
- 62
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
The title compound, C 14 H 12 O 2 S, was prepared by the oxidation of 2-methyl-1-(methylsulfanyl)naphtho[2,1-b]furan using m-chloroperbenzoic acid. The crystal structure contains aromaticstacking, C-HÁ Á ÁO and C-HÁ Á Á interactions.
📜 SIMILAR VOLUMES
The title compound, C 19 H 13 BrOS, was prepared by the Lewis acid-catalysed reaction of 6-bromo-2-naphthol with 2-chloro-2-(methylsulfanyl)acetophenone. The naphthofuran ring system is nearly planar. The crystal structure is stabilized by a C-HÁ Á Á interaction.
The title compound, C~21~H~16~N~2~O~5~, was synthesized by the reaction of 2-naphthol with methyl cyanoacetate and 3-nitrobenzaldehyde in ethanol under microwave irradiation. The pyran ring adopts a boat conformation.