Chemo, stereo, and regioselective addition of α-(2-methoxyaryl)-N-aryl nitrones to diarylidineacetone: Synthesis of novel isoxazolidines
✍ Scribed by Sadaiyan Ramadass Jayapradha; Vellaisamy Sridharan; Shanmugam Muthusubramanian; Kurt Polborn
- Book ID
- 102339299
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2007
- Tongue
- English
- Weight
- 287 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Abstract
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A new set of 2,3,4,5‐tetrasubstituted isoxazolidines with an α,β‐unsaturated carbonyl function at position 4 has been synthesized. The multicomponent approach and microwave irradiation protocol have also been investigated for the above synthesis.
📜 SIMILAR VOLUMES
The synthesis of 2-phenyl-3-aryl and 2-phenyl-3-aroyl derivatives 5-(1,2-O-isopropylidene-alpha-D-xylo-tetrofuranos-4-yl)isoxazolidi ne (3) from nitrones and 5,6-dideoxy-1,2-O-isopropylidene-alpha-D-xylo-hex-5- enofuranose (1) is described. The 1,3-dipolar cycloaddition reactions given mainly anti a
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