HIGHLY EFFICIENT ASYMMETRIC REDUCTION OF ALPHA-TERTIARY ALKYL KETONES WITH DIISOPINOCAMPHEYLCHLOROBORANE

[1] POTASSIUM - 9-O-(1,2-5,6-DI-O-ISOPROPYLIDENE-ALPHA-D-GLUCOFURANOSYL)-9-BORATABICYCLO[3.3.1]NONANE - A NEW, EFFECTIVE CHIRAL BOROHYDRIDE REAGENT [J]. JOURNAL OF ORGANIC CHEMISTRY, 1986, 51 (10) : 1934 - 1936

[2] SELECTIVE REDUCTIONS .37. ASYMMETRIC REDUCTION OF PROCHIRAL KETONES WITH B-(3-PINANYL)-9-BORABICYCLO[3.3.1]NONANE [J]. JOURNAL OF ORGANIC CHEMISTRY, 1985, 50 (09) : 1384 - 1394

[3] BROWN HC, 1975, ORGANIC SYNTHESES VI, pCH9

[4] DIISOPINOCAMPHEYLCHLOROBORANE, A REMARKABLY EFFICIENT CHIRAL REDUCING AGENT FOR AROMATIC PROCHIRAL KETONES [J]. JOURNAL OF ORGANIC CHEMISTRY, 1985, 50 (25) : 5446 - 5448

[5] STEREOSELECTIVE SYNTHESIS OF ALCOHOLS .9. ABSOLUTE-CONFIGURATION OF STEGOBINONE [J]. CHEMISCHE BERICHTE-RECUEIL, 1981, 114 (08): : 2786 - 2801

[6] ISTUNO S, 1985, J CHEM SOC P1, P2039

[7] THERMOSTABLE ENZYMES IN ORGANIC-SYNTHESIS .2. ASYMMETRIC REDUCTION OF KETONES WITH ALCOHOL-DEHYDROGENASE FROM THERMOANAEROBIUM-BROCKII [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1986, 108 (01) : 162 - 169

[8] NB-ENANTRIDE, A NEW CHIRAL TRIALKYLBOROHYDRIDE FOR THE ASYMMETRIC REDUCTION OF KETONES [J]. JOURNAL OF ORGANIC CHEMISTRY, 1982, 47 (12) : 2495 - 2496

[9] MIDLAND MM, 1978, J ORGANOMET CHEM, V156, P203, DOI 10.1016/S0022-328X(00)84877-9

[10] ASYMMETRIC REDUCTION OF PROCHIRAL KETONES WITH B-3-PINANYL-9-BORABICYCLO[3.3.1]NONANE IN EFFICIENCIES APPROACHING 100-PERCENT - SIMULTANEOUS RATE ENHANCEMENT AND SIDE REACTION SUPPRESSION VIA THE USE OF ELEVATED PRESSURES [J]. JOURNAL OF ORGANIC CHEMISTRY, 1984, 49 (07) : 1316 - 1317

[1] POTASSIUM - 9-O-(1,2-5,6-DI-O-ISOPROPYLIDENE-ALPHA-D-GLUCOFURANOSYL)-9-BORATABICYCLO[3.3.1]NONANE - A NEW, EFFECTIVE CHIRAL BOROHYDRIDE REAGENT [J]. JOURNAL OF ORGANIC CHEMISTRY, 1986, 51 (10) : 1934 - 1936

[2] SELECTIVE REDUCTIONS .37. ASYMMETRIC REDUCTION OF PROCHIRAL KETONES WITH B-(3-PINANYL)-9-BORABICYCLO[3.3.1]NONANE [J]. JOURNAL OF ORGANIC CHEMISTRY, 1985, 50 (09) : 1384 - 1394

[3] BROWN HC, 1975, ORGANIC SYNTHESES VI, pCH9

[4] DIISOPINOCAMPHEYLCHLOROBORANE, A REMARKABLY EFFICIENT CHIRAL REDUCING AGENT FOR AROMATIC PROCHIRAL KETONES [J]. JOURNAL OF ORGANIC CHEMISTRY, 1985, 50 (25) : 5446 - 5448

[5] STEREOSELECTIVE SYNTHESIS OF ALCOHOLS .9. ABSOLUTE-CONFIGURATION OF STEGOBINONE [J]. CHEMISCHE BERICHTE-RECUEIL, 1981, 114 (08): : 2786 - 2801

[6] ISTUNO S, 1985, J CHEM SOC P1, P2039

[7] THERMOSTABLE ENZYMES IN ORGANIC-SYNTHESIS .2. ASYMMETRIC REDUCTION OF KETONES WITH ALCOHOL-DEHYDROGENASE FROM THERMOANAEROBIUM-BROCKII [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1986, 108 (01) : 162 - 169

[8] NB-ENANTRIDE, A NEW CHIRAL TRIALKYLBOROHYDRIDE FOR THE ASYMMETRIC REDUCTION OF KETONES [J]. JOURNAL OF ORGANIC CHEMISTRY, 1982, 47 (12) : 2495 - 2496

[9] MIDLAND MM, 1978, J ORGANOMET CHEM, V156, P203, DOI 10.1016/S0022-328X(00)84877-9

[10] ASYMMETRIC REDUCTION OF PROCHIRAL KETONES WITH B-3-PINANYL-9-BORABICYCLO[3.3.1]NONANE IN EFFICIENCIES APPROACHING 100-PERCENT - SIMULTANEOUS RATE ENHANCEMENT AND SIDE REACTION SUPPRESSION VIA THE USE OF ELEVATED PRESSURES [J]. JOURNAL OF ORGANIC CHEMISTRY, 1984, 49 (07) : 1316 - 1317