AAAAAA

   
Results: 1-3 |
Results: 3
THE HYDROXYPINANONE AS CHIRAL AUXILIARY IN MICHAEL ADDITIONS - AN INVERSION OF DIASTEREOSELECTIVITY AT LOW CONCENTRATION OF ENOLATE, A SUBSTRATE-DIRECTED APPROACH
Authors: SOLLADIECAVALLO A KOESSLER JL ISARNO T ROCHE D ANDRIAMIADANARIVO R
Citation: A. Solladiecavallo et al., THE HYDROXYPINANONE AS CHIRAL AUXILIARY IN MICHAEL ADDITIONS - AN INVERSION OF DIASTEREOSELECTIVITY AT LOW CONCENTRATION OF ENOLATE, A SUBSTRATE-DIRECTED APPROACH, Synlett, (2), 1997, pp. 217
ERYTHRO-SELECTIVE ALDOL CONDENSATION USING DIRECTLY GENERATED TI-ENOLATES - APPLICATION TO THE SYNTHESIS OF PURE (1R,2S)-CHLORAMPHENICOL BASE AND (2R,3R) ALLO-THREONINE
Authors: SOLLADIECAVALLO A KOESSLER JL FISCHER J DECIAN A
Citation: A. Solladiecavallo et al., ERYTHRO-SELECTIVE ALDOL CONDENSATION USING DIRECTLY GENERATED TI-ENOLATES - APPLICATION TO THE SYNTHESIS OF PURE (1R,2S)-CHLORAMPHENICOL BASE AND (2R,3R) ALLO-THREONINE, Gazzetta chimica italiana, 126(3), 1996, pp. 173-178
A 4-STEP DIASTEREOSELECTIVE SYNTHESIS OF D-ERYTHRO-SPHINGOSINE BY AN ENANTIOSELECTIVE ALDOL REACTION USING A TITANIUM ENOLATE DERIVED FROM A CHIRAL IMINOGLYCINATE
Authors: SOLLADIECAVALLO A KOESSLER JL
Citation: A. Solladiecavallo et Jl. Koessler, A 4-STEP DIASTEREOSELECTIVE SYNTHESIS OF D-ERYTHRO-SPHINGOSINE BY AN ENANTIOSELECTIVE ALDOL REACTION USING A TITANIUM ENOLATE DERIVED FROM A CHIRAL IMINOGLYCINATE, Journal of organic chemistry, 59(11), 1994, pp. 3240-3242
Risultati: 1-3 |