The synthesis and spectra of new (E)-(trans) and (Z)-(cis)-1-alkyl-2-aryl (alkyl) - 3 -aroylaziridines
โ Scribed by Philip Tarburton; Lori J. Wolpa; Robert K. Loerch; Thomas L. Folsom; Norman H. Cromwell
- Book ID
- 112125140
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 1977
- Tongue
- English
- Weight
- 427 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0022-152X
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๐ SIMILAR VOLUMES
The title compounds were stereoselectively synthesized via a semi-benzilic Favorskii rearrangement of 3-aryl-and 3-alkyl-2,2-dichlorocyclobutanols, obtained by stereoselective reduction of the corresponding cyclobutanones. This synthetic pathway, starting from the synthesis of 3-substituted-2,2-dich
The title cyclic b-amino esters were synthesized stereo-and regioselectively. Starting from the corresponding 1-aryl-and 1-alkylcyclopropane-1,2-dicarboxylates, selective monosaponification and subsequent Curtius reaction leads to certain cis-1-alkyland 1-aryl-2-aminocyclopropanecarboxylic esters. T
## Abstract For Abstract see ChemInform Abstract in Full Text.