pyrroles can be prepared in stereocontrolled fashions by the reaction of 2-amino-l-(l-phenylvlnyl)cyclohexanols with formaldehyde and acid. Recent papers from our laboratory have described the use of "Mannich-directed" cationic aza-Cope rearrangements for the preparation of octahydroindolones by an
Synthesis applications of aza-cope rearrangements. Stereoselective synthesis of trans-alkyl-cis-3a-aryloctahydroindolones.
โ Scribed by Larry E Overman; Leah T Mendelson; Lee A Flippin
- Publisher
- Elsevier Science
- Year
- 1982
- Tongue
- French
- Weight
- 215 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
The reaction of both cis-and trans-2-amino-l-(l-phenylvinyl)cyclopentanols with aldehydes affords trans-2-alkyl-cis-3a-aryl-4-oxo-octahydro indoles stereoselectively.
๐ SIMILAR VOLUMES
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.