UNIQUE CATALYSIS BY EU(DPPM)3 - CATALYTIC MOLECULAR RECOGNITION IN ALDOL AND MICHAEL REACTIONS

[1] MILD LEWIS ACID CATALYSIS - EU(FOD)3-MEDIATED HETERO-DIELS-ALDER REACTION [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1983, 105 (11) : 3716 - 3717

[2] ORGANOLANTHANIDE CATALYSIS OF A MUKAIYAMA ADDITION-REACTION [J]. JOURNAL OF ORGANIC CHEMISTRY, 1990, 55 (26) : 6235 - 6236

[3] ACYCLIC STEREOSELECTION .29. STEREOSELECTION IN THE MICHAEL ADDITION-REACTION .1. THE MOKAIYAMA MICHAEL RECTION [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1985, 107 (09) : 2797 - 2799

[4] ACYCLIC STEREOSELECTION .4. ASSIGNMENT OF STEREOSTRUCTURE TO BETA-HYDROXYCARBONYL COMPOUNDS BY C-13 NUCLEAR MAGNETIC-RESONANCE [J]. JOURNAL OF ORGANIC CHEMISTRY, 1979, 44 (24) : 4294 - 4299

[5] OPTICALLY-ACTIVE DI(PERFLUORO-2-PROPOXYPROPIONYL)METHANE - A NOVEL LIGAND FOR NMR SHIFT-REAGENT [J]. CHEMISTRY LETTERS, 1982, (02) : 153 - 156

[6] CLAY MONTMORILLONITE-CATALYZED ALDOL REACTIONS OF SILYL ENOL ETHERS WITH ALDEHYDES AND ACETALS [J]. CHEMISTRY LETTERS, 1986, (09) : 1581 - 1584

[7] THE CHEMISTRY OF ORTHO-SILYLATED KETENE ACETALS - DIASTEREOSELECTIVE ALDOL REACTION OF 2,3-O-ISOPROPYLIDENE-D (AND L)-GLYCERALDEHYDES LEADING TO 2-DEOXY-D (AND L)-RIBOSES [J]. TETRAHEDRON LETTERS, 1985, 26 (47) : 5777 - 5780

[8] AMPHIPHILIC REACTIONS BY MEANS OF EXCEPTIONALLY BULKY ORGANO-ALUMINUM REAGENTS - RATIONAL APPROACH FOR OBTAINING UNUSUAL EQUATORIAL, ANTI-CRAM, AND 1,4 SELECTIVITY IN CARBONYL ALKYLATION [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1988, 110 (11) : 3588 - 3597

[9] MIDLAND MM, 1984, J AM CHEM SOC, V106, P4294, DOI 10.1021/ja00327a054

[10] CATALYTIC ASYMMETRIC ALDOL REACTION OF SILYL ENOL ETHERS WITH ALDEHYDES BY THE USE OF CHIRAL DIAMINE COORDINATED TIN(II) TRIFLATE [J]. CHEMISTRY LETTERS, 1990, (01) : 129 - 132

[1] MILD LEWIS ACID CATALYSIS - EU(FOD)3-MEDIATED HETERO-DIELS-ALDER REACTION [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1983, 105 (11) : 3716 - 3717

[2] ORGANOLANTHANIDE CATALYSIS OF A MUKAIYAMA ADDITION-REACTION [J]. JOURNAL OF ORGANIC CHEMISTRY, 1990, 55 (26) : 6235 - 6236

[3] ACYCLIC STEREOSELECTION .29. STEREOSELECTION IN THE MICHAEL ADDITION-REACTION .1. THE MOKAIYAMA MICHAEL RECTION [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1985, 107 (09) : 2797 - 2799

[4] ACYCLIC STEREOSELECTION .4. ASSIGNMENT OF STEREOSTRUCTURE TO BETA-HYDROXYCARBONYL COMPOUNDS BY C-13 NUCLEAR MAGNETIC-RESONANCE [J]. JOURNAL OF ORGANIC CHEMISTRY, 1979, 44 (24) : 4294 - 4299

[5] OPTICALLY-ACTIVE DI(PERFLUORO-2-PROPOXYPROPIONYL)METHANE - A NOVEL LIGAND FOR NMR SHIFT-REAGENT [J]. CHEMISTRY LETTERS, 1982, (02) : 153 - 156

[6] CLAY MONTMORILLONITE-CATALYZED ALDOL REACTIONS OF SILYL ENOL ETHERS WITH ALDEHYDES AND ACETALS [J]. CHEMISTRY LETTERS, 1986, (09) : 1581 - 1584

[7] THE CHEMISTRY OF ORTHO-SILYLATED KETENE ACETALS - DIASTEREOSELECTIVE ALDOL REACTION OF 2,3-O-ISOPROPYLIDENE-D (AND L)-GLYCERALDEHYDES LEADING TO 2-DEOXY-D (AND L)-RIBOSES [J]. TETRAHEDRON LETTERS, 1985, 26 (47) : 5777 - 5780

[8] AMPHIPHILIC REACTIONS BY MEANS OF EXCEPTIONALLY BULKY ORGANO-ALUMINUM REAGENTS - RATIONAL APPROACH FOR OBTAINING UNUSUAL EQUATORIAL, ANTI-CRAM, AND 1,4 SELECTIVITY IN CARBONYL ALKYLATION [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1988, 110 (11) : 3588 - 3597

[9] MIDLAND MM, 1984, J AM CHEM SOC, V106, P4294, DOI 10.1021/ja00327a054

[10] CATALYTIC ASYMMETRIC ALDOL REACTION OF SILYL ENOL ETHERS WITH ALDEHYDES BY THE USE OF CHIRAL DIAMINE COORDINATED TIN(II) TRIFLATE [J]. CHEMISTRY LETTERS, 1990, (01) : 129 - 132