STEREOSELECTIVE ALPHA-METHYLATION OF N-METHYL BENZYLAMINE VIA A COMBINATION OF CHROMIUM TRICARBONYL AND CHIRAL FORMAMIDINE METHODOLOGIES

Podobne zapisy

• ALPHA-STEREOSELECTIVE TANDEM ADDITIONS TO (ORTHO-METHOXYSTYRENE) CHROMIUM TRICARBONYL
  od: Davies, S, i wsp.
  Wydane: (1995)
• ASYMMETRIC-SYNTHESIS OF (R)-(+)-ALPHA-METHYL-O-METHOXYBENZYL METHYL-ETHER VIA THE STEREOSELECTIVE BENZYLIC ELABORATION OF TRICARBONYL (ETA-6-O-METHOXYBENZYL METHYL ETHER)CHROMIUM(O)
  od: Davies, S, i wsp.
  Wydane: (1992)
• PYRIDINE CHROMIUM TRICARBONYL COMPLEXES - COMPLETELY STEREOSELECTIVE ALPHA,ALPHA-DIALKYLATION OF 2-METHYLPYRIDINE TRICARBONYLCHROMIUM
  od: Davies, S, i wsp.
  Wydane: (1990)
• STEREOSELECTIVE SYNTHESIS VIA ARENE CHROMIUM TRICARBONYL COMPLEXES
  od: Davies, S
  Wydane: (1986)
• Stereoselective methodology for 1-aryl-1-alkyl epoxides via chromium tricarbonyl complexes
  od: Davies, S, i wsp.
  Wydane: (1997)