Asymmetric conjugate addition of organocopper-amidophosphine reagents to cycloalkenones
β Scribed by Motomu Kanai; Kiyoshi Tomioka
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- French
- Weight
- 322 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Mediated by a noncovalently bound chiral amidophosphine iigand I, reaction of organocoppers with cycloalkenones 2 aforded the corresponding J-substituted cyclo-aLk-anones 3 in 9568% ee.
π SIMILAR VOLUMES
Two types of external, chiral amidophosphine ligands, 1-5, were prepared. Examination of their behavior in an asymmetric conjugate addition reaction of organocuprate revealed the possibility for steric tuning to realize high selectivity.
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