The rates and stereochemistry of ring closure of the radicah (21, (Lj), Cl\_?), and (161 have been detemined and rationalised. Recently,l we suggested that 1,5-ring closures of substituted hex-5-enyl radicals and related acyclic species are stereoselective: l-or 3-substituted systems give mainly ci
โฆ LIBER โฆ
Formation of tetrahydroindanes and related systems by methods involving radical ring closure
โ Scribed by Beckwith, Athelstan L. J.; O'Shea, Dennis M.; Roberts, David H.
- Book ID
- 121080367
- Publisher
- The Royal Society of Chemistry
- Year
- 1983
- Tongue
- English
- Weight
- 202 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0022-4936
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