Thiophenol-Promoted Radical Cyclization of Hydrazones and Oxime Ethers. -Ethylenic and acetylenic tethered hydrazones or oxime ethers undergo a thiophenol radical induced cyclization providing a number of carbaor heterocyclic products.
ChemInform Abstract: Tributyltin Hydride-Mediated Free-Radical Cyclization of Allene- Tethered Oxime Ethers and Hydrazones.
β Scribed by J. MARCO-CONTELLES; G. BALME; D. BOUYSSI; C. DESTABEL; C. D. HENRIET-BERNARD; J. GRIMALDI; J. M. HATEM
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 37 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
Tributyltin Hydride-Mediated Free-Radical Cyclization of Allene-Tethered Oxime Ethers and Hydrazones.
-It offers a convenient method to prepare (vinylstannyl) cyclopentylamine derivatives. The sitedirected intermolecular attack of the tributyltin radical at the allene moiety and the final size of the ring after cycloisomerization is found to depend on the substitution pattern. Treatment of the products with HCl gives the corresponding destannylated derivatives in good yields. -(MARCO-CONTELLES, J.;
π SIMILAR VOLUMES
A Concise Synthesis of Rigidified Ξ²-Amino Acids via Sulfanyl Radical Addition-Cyclization of Oxime Ethers and Hydrazones. -Sulfanyl radical cyclization of alkenyl-tethered oxime ethers and hydrazones (I) provides cis/trans mixtures of the cyclized products (III) and (IV). The cyclopentylamines (III
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