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ChemInform Abstract: Tributyltin Hydride-Mediated Free-Radical Cyclization of Allene- Tethered Oxime Ethers and Hydrazones.

✍ 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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✦ 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.;


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