Stereoselective synthesis of cis- and trans-3-fluoro-1-phenylcyclobutyl amine
โ Scribed by Pengcheng P. Shao; Feng Ye
- Book ID
- 104095304
- Publisher
- Elsevier Science
- Year
- 2008
- Tongue
- French
- Weight
- 119 KB
- Volume
- 49
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
A stereoselective approach to the synthesis of cis-and trans-3-fluoro-1-phenylcyclobutylamine has been developed. Excellent stereoselectivity was obtained by the reduction of the appropriately substituted cyclobutanone to give either cis-or trans-isomers of 3-hydroxyl-1-phenylcyclobutylamine, which was stereoselectively converted to the 3-fluoro derivative.
๐ SIMILAR VOLUMES
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Swnmary : The organotin reagent from I-chloro-3-iodoprop-l-ene and SnClz in dimethyZformamide reacted with aldehydes by its chlorine-substituted carbon atom. Treatment with NaOMe then gave cis vinyloxiranes with good stereo-selectivity. Benzaldehyde and I-bromo-3-iodoprop-l-ene in the presence of tw