A highly efficient aminohydroxylation process

[1] 1,2-amino alcohols and their heterocyclic derivatives as chiral auxiliaries in asymmetric synthesis [J]. CHEMICAL REVIEWS, 1996, 96 (02) : 835 - 875

[2] [Anonymous], ANGEW CHEM INT EDIT, DOI DOI 10.1002/ANIE.199622881

[3] BACKVALL JE, 1979, J ORG CHEM, V44, P1953

[4] Balkenhohl F., 1996, ANGEW CHEM, V108, P2436

[5] A new ligand class for the asymmetric dihydroxylation of olefins [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1996, 35 (04): : 448 - 451

[6] BECKER H, 1996, ANGEW CHEM, V108, P447

[7] ASYMMETRIC DIHYDROXYLATION (AD) OF N,N-DIALKYL AND N-METHOXY-N-METHYL ALPHA,BETA-UNSATURATED AND BETA,GAMMA-UNSATURATED AMIDES [J]. TETRAHEDRON LETTERS, 1993, 34 (13) : 2079 - 2082

[8] BROOK MA, 1983, SYNTHESIS-STUTTGART, P201

[9] N-bromoacetamide - A new nitrogen source for the catalytic asymmetric aminohydroxylation of olefins [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1997, 36 (13-14): : 1483 - 1486

[10] Bruncko M., 1997, ANGEW CHEM, V109, P1580

[1] 1,2-amino alcohols and their heterocyclic derivatives as chiral auxiliaries in asymmetric synthesis [J]. CHEMICAL REVIEWS, 1996, 96 (02) : 835 - 875

[2] [Anonymous], ANGEW CHEM INT EDIT, DOI DOI 10.1002/ANIE.199622881

[3] BACKVALL JE, 1979, J ORG CHEM, V44, P1953

[4] Balkenhohl F., 1996, ANGEW CHEM, V108, P2436

[5] A new ligand class for the asymmetric dihydroxylation of olefins [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1996, 35 (04): : 448 - 451

[6] BECKER H, 1996, ANGEW CHEM, V108, P447

[7] ASYMMETRIC DIHYDROXYLATION (AD) OF N,N-DIALKYL AND N-METHOXY-N-METHYL ALPHA,BETA-UNSATURATED AND BETA,GAMMA-UNSATURATED AMIDES [J]. TETRAHEDRON LETTERS, 1993, 34 (13) : 2079 - 2082

[8] BROOK MA, 1983, SYNTHESIS-STUTTGART, P201

[9] N-bromoacetamide - A new nitrogen source for the catalytic asymmetric aminohydroxylation of olefins [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1997, 36 (13-14): : 1483 - 1486

[10] Bruncko M., 1997, ANGEW CHEM, V109, P1580