Control of chemo- and regio-selectivity in rhodium catalysed reactions of unsaturated amines with H2CO
โ Scribed by David J. Bergmann; Eva M. Campi; W.Roy Jackson; Quentin J. McCubbin; Antonio F. Patti
- Book ID
- 104257249
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 148 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
The rhodium catalysed reactions of N-allyl-and N-butenyl-l,3-diaminopropanes give single products arising from exclusive hydroformylation at the terminal carbon when the hindered bisphosphite ligand, BIPHEPHOS is used. Reactions using a high carbon monoxide : hydrogen ratio (9 : I) and triphenylphosphine as ligand give predominantly lactams arising from carbonylation but with poor control of regioselectivity.
๐ SIMILAR VOLUMES
By treatment with organocopper reagents, N-activated 2,3-cis-3-alkyl-2-vinylaziridines produced exclusively (E)-allyl amines in high yields, presumably via an anti-SN2' reaction pathway. On the other hand, under otherwise identical conditions, N-activated 2,3-trans-3-alkyl-2-vinylazaridines gave an