Stereoselective synthesis of .alpha.-alkylazetidinones by a free radical chain reaction
β Scribed by Sacripante, Guerino; Just, George
- Book ID
- 126278790
- Publisher
- American Chemical Society
- Year
- 1987
- Tongue
- English
- Weight
- 437 KB
- Volume
- 52
- Category
- Article
- ISSN
- 0022-3263
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π SIMILAR VOLUMES
Cyclopropanation is regarded as an important transformation in organic synthesis. [1] Synthesis of 3-azabicyclo-A C H T U N G T R E N N U N G [3.1.0]hexane structures has been of interest because compounds with these structures, for example, indolizomycin, [2] trovafloxacin, [3] duocarmycin, and CC-
Stereoselective Synthesis of (Β±)-Ξ±-Kainic Acid Using Free Radical Key Reactions. -The title compound (XI) is obtained via two routes from the highly substituted isocyanide and the isothiocyanate (XII) via the common intermediate (IX). In both routes the key synthons (cf. (IV) and (XIV)) are obtained