Radical cyclisation of 2,6-dinitroalkanes
โ Scribed by W.Russell Bowman; Stuart W. Jackson
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- French
- Weight
- 252 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Synthesis of compounds structurally related to morphine is a field of lasting interest to many chemists. These substances form a well-known class of analgesics2 which can possess properties of antagonism to narcotics3 and which includes phenazocine4 and pentazocine5 of medicinal use. The Grewe synth
Radical cycliitions of various methylenecycbpopane derivatives have been stdied and it has been fotmd that methylenecyc~l pfopyl radicals undergo exclusive 5-cx0 cydhtion while methylenecycloppyl butyl mdicala give a mixtme of product9 resulting tium f&x0 and 7-efdo cyclisation. Attempted cyclisatio
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