Highly Diastereoselective Arylation of (S)-Mandelic Acid Enolate: Enantioselective Synthesis of Substituted (R)-3-Hydroxy-3-phenyloxindoles and (R)-Benzylic Acids …
S Barroso, G Blay, L Cardona, I Fernández…
Index: Langer, Peter; Holtz, Edith Synlett, 2003 , # 3 p. 402 - 404
Full Text: HTML
Citation Number: 38
Abstract
... optically active (S)-mandelic acid and pivalaldehyde with several o- and p-halonitrobenzenes proceeds ... of the dioxolanone moiety leads directly to enantiomerically pure (R)-3-hydroxy-3- phenyloxindoles. ... as terminal oxidant in the presence of pivalaldehyde and the Co(III)-Me 2 ...
Related Articles:
Domino 'Michael-retro-Michael-aldol'reactions of 1, 3-bis-silyl enol ethers with 3-formylchromones
[Langer, Peter; Appel, Bettina Tetrahedron Letters, 2003 , vol. 44, # 43 p. 7921 - 7923]