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Is an iodine atom almighty as a leaving group for Bu (sub)3 SnH-mediated radical cyclization? The effect of a halogen atom on the 5-endo-trig radical cyclization of N-vinyl-alpha-halo amides
- Source :
- Journal of Organic Chemistry. August 9, 2002, Vol. 67 Issue 16, p5537, 9 p.
- Publication Year :
- 2002
-
Abstract
- Research has been conducted on the halogen atoms. The role of this atom as a leaving group in Bu (sub)3 SnH-mediated radical cyclization of N-(cyclohex-1-enyl) alpha-halo amides has been investigated and the details are reported.
- Subjects :
- Chemistry, Organic -- Research
Iodine -- Physiological aspects
Radicals (Chemistry) -- Physiological aspects
Ring formation (Chemistry) -- Physiological aspects
Tin -- Physiological aspects
Hydrogen -- Physiological aspects
Halogens -- Physiological aspects
Amides -- Physiological aspects
Biological sciences
Chemistry
Subjects
Details
- ISSN :
- 00223263
- Volume :
- 67
- Issue :
- 16
- Database :
- Gale General OneFile
- Journal :
- Journal of Organic Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- edsgcl.90825474