An enantioselective process for the preparation of chiral triaryl derivatives and chiral intermediates for use therein

作者: John Clifford Head , Graham John Warrellow , John Robert Porter , Rikki Peter Alexander , Ewan Campbell Boyd

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摘要: An enantioselective multi-stage process is described which uses as a starting material an α,β-unsaturated olefin of the formula (1): Ar-CH=C(R4)COAux, where Ar and R4, may be same or different, each monocyclic bicyclic aryl group optionally containing one more heteroatoms selected from oxygen, sulphur nitrogen atoms; Aux residue chiral (R- S-) auxiliary. In process, converted to triarylethane are useful PDE IV inhibitors.

参考文章(42)
Bernhard Zipperer, Gisela Lorenz, Thomas Zierke, Eberhard Ammermann, Norbert Goetz, Manfred Lauer, Hetarylalkenes, their preparation and intermediates for their preparation, and their use ,(1991)
David Waterson, Alkanoic acid derivatives ,(1992)
G P Livi, P Kmetz, M M McHale, L B Cieslinski, G M Sathe, D P Taylor, R L Davis, T J Torphy, J M Balcarek, Cloning and expression of cDNA for a human low-Km, rolipram-sensitive cyclic AMP phosphodiesterase Molecular and Cellular Biology. ,vol. 10, pp. 2678- 2686 ,(1990) , 10.1128/MCB.10.6.2678
Fredric J. Vinick, Nicholas A. Saccomano, Aryl substituted nitrogen heterocyclic antidepressants ,(1991)