Novel concepts in directed biaryl synthesis, XXXVII. Synthesis and enantiomerization of a nonracemic 2-hydroxy-2′-biarylcarbaldehyde, a probable intermediate in the atropo-enantioselective ring opening of biaryl lactones
- 11 March 1994
- journal article
- research article
- Published by Wiley in European Journal of Organic Chemistry
- Vol. 1994 (3) , 313-316
- https://doi.org/10.1002/jlac.199419940314
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- Atropo-enantioselective biaryl synthesis by stereocontrolled cleavage of configuratively labile lactone-bridged precursors using chiral H-nucleophilesTetrahedron, 1993
- An efficient and catalytically enantioselective route to (S)-(-)-phenyloxiraneThe Journal of Organic Chemistry, 1988
- A stable and easily prepared catalyst for the enantioselective reduction of ketones. Applications to multistep synthesesJournal of the American Chemical Society, 1987
- Isolierbare KonformationsisomereChemie in Unserer Zeit, 1983