Synthesis of 2- and 3-alkyl(aryl)-cis-1-thiadecalins
โ Scribed by N. P. Volynskii; L. A. Zegel'man; M. B. Smirnov
- Book ID
- 112444859
- Publisher
- Springer
- Year
- 1989
- Tongue
- English
- Weight
- 522 KB
- Volume
- 38
- Category
- Article
- ISSN
- 1573-9171
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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.