DIASTEREOSELECTIVE 3-CENTER MICHAEL ADDITION OF BETA-KETOESTERS TO PROSTEREOGENIC ALPHA,BETA-UNSATURATED CARBONYL-COMPOUNDS CATALYZED BY K2CO3 OR CS2CO3
被引:16
作者:
OUVRARD, N
论文数: 0引用数: 0
h-index: 0
机构:
CNRS, SYNTHESE ORGAN LAB, CTR ST JEROME BOITE D12, F-13397 MARSEILLE 13, FRANCECNRS, SYNTHESE ORGAN LAB, CTR ST JEROME BOITE D12, F-13397 MARSEILLE 13, FRANCE
OUVRARD, N
[1
]
RODRIGUEZ, J
论文数: 0引用数: 0
h-index: 0
机构:
CNRS, SYNTHESE ORGAN LAB, CTR ST JEROME BOITE D12, F-13397 MARSEILLE 13, FRANCECNRS, SYNTHESE ORGAN LAB, CTR ST JEROME BOITE D12, F-13397 MARSEILLE 13, FRANCE
RODRIGUEZ, J
[1
]
SANTELLI, M
论文数: 0引用数: 0
h-index: 0
机构:
CNRS, SYNTHESE ORGAN LAB, CTR ST JEROME BOITE D12, F-13397 MARSEILLE 13, FRANCECNRS, SYNTHESE ORGAN LAB, CTR ST JEROME BOITE D12, F-13397 MARSEILLE 13, FRANCE
SANTELLI, M
[1
]
机构:
[1] CNRS, SYNTHESE ORGAN LAB, CTR ST JEROME BOITE D12, F-13397 MARSEILLE 13, FRANCE
The stereocontrolled construction of three contiguous quaternary and tertiary carbon atoms is possible by the title reaction [Eq. (a)]. The diastereoselectivity can be reversed by the addition of crown ethers or other cryptands. R1 = Me, tBu, Bz; R2 = H, Me.