## Abstract magnified image Reaction of (4__E__)‐4‐arylmethylene‐3,4‐dihydro‐1‐benzothiepin‐5(2__H__)‐ones **3a‐e** with nitrilimines (generated __in situ via__ triethylamine dehydrohalogenation of the corresponding hydrazonoyl chlorides **4a, b**) in refluxing benzene, afforded 2′,4′,5′‐triaryl‐2
✦ LIBER ✦
Regio- and Stereoselective Synthesis of Spiro[1-benzothiepine-4(5H),3′(3H)-pyrazol]-5-ones.
✍ Scribed by Nawal Mishriky; Adel S. Girgis; Hanaa M. Hosni; Hanaa Farag
- Publisher
- John Wiley and Sons
- Year
- 2007
- Weight
- 17 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0931-7597
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✦ Synopsis
Abstract
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📜 SIMILAR VOLUMES
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## Abstract magnified image A series of seven new 2′,3′,4′‐substituted spiro[isothiochromene‐3,5′‐isoxazolidin]‐4(1__H__)‐ones (**7‐13**) has been prepared in the reaction of benzylidene(phenyl)azane oxide (**5**) or benzylidene(methyl)azane oxide (**6**) with (3Z)‐3‐(4‐substituted‐benzylidene)‐1_