ChemInform Abstract: Palladium Asymmetric Reduction of β-Carboline Imines Mediated by Chiral Auxiliaries Assisted Microwave Irradiation.

Palladium asymmetric reduction of β-carboline imines mediated by chiral auxiliaries assisted by microwave irradiation

Tetrahedron Letters ◽

10.1016/j.tetlet.2009.09.181 ◽

2009 ◽

Vol 50 (50) ◽

pp. 7059-7061 ◽

Cited By ~ 14

Author(s):

Marlene Espinoza-Moraga ◽

Ana Gloria Caceres ◽

Leonardo Silva Santos

Keyword(s):

Microwave Irradiation ◽

Asymmetric Reduction ◽

ChemInform Abstract: Novel Camphor-Derived Chiral Auxiliaries: Significant Solvent and Additive Effects on Asymmetric Reduction of Chiral α-Keto Esters.

ChemInform ◽

10.1002/chin.200006055 ◽

2010 ◽

Vol 31 (6) ◽

pp. no-no

Author(s):

Ying-Yuan Chu ◽

Chia-Sheng Yu ◽

Chiou-Juy Chen ◽

Kung-Shuo Yang ◽

Jung-Chaing Lain ◽

...

Keyword(s):

Asymmetric Reduction ◽

Additive Effects ◽

Chiral Auxiliaries ◽

ChemInform Abstract: Homochiral NADH Models in the Pyrrolo[2,3-b]pyridine Series Bearing One or Two Chiral Auxiliaries. Asymmetric Reduction of Methyl Benzoylformate and N-Acetyl-enamines. Influence of the Magnesium Salt Concentration on the Asymmetric In

ChemInform ◽

10.1002/chin.199806124 ◽

2010 ◽

Vol 29 (6) ◽

pp. no-no

Author(s):

C. LEROY ◽

V. LEVACHER ◽

G. DUPAS ◽

G. QUEGUINER ◽

J. BOURGUIGNON

Keyword(s):

Salt Concentration ◽

Asymmetric Reduction ◽

Magnesium Salt ◽

Chiral Auxiliaries ◽

Pyridine Series ◽

Methyl Benzoylformate

ChemInform Abstract: New Chiral Auxiliaries Derived from β-Pinene: Their Use in the Asymmetric Reduction of β-Keto Esters.

ChemInform ◽

10.1002/chin.199137057 ◽

2010 ◽

Vol 22 (37) ◽

pp. no-no

Author(s):

M. L. VASCONCELLOS ◽

J. D'ANGELO ◽

D. DESMAELE ◽

P. R. R. COSTA ◽

D. POTIN

Keyword(s):

Asymmetric Reduction ◽

Chiral Auxiliaries ◽

Homochiral NADH models in the pyrrolo[2,3-b]pyridine series bearing one or two chiral auxiliaries. Asymmetric reduction of methyl benzoylformate and N-acetyl-enamines. Influence of the magnesium salt concentration on the asymmetric induction of reductions

Tetrahedron Asymmetry ◽

10.1016/s0957-4166(97)00436-9 ◽

1997 ◽

Vol 8 (19) ◽

pp. 3309-3318 ◽

Cited By ~ 10

Author(s):

Corine Leroy ◽

Vincent Levacher ◽

Georges Dupas ◽

Guy Quéguiner ◽

Jean Bourguignon

Keyword(s):

Salt Concentration ◽

Asymmetric Reduction ◽

Asymmetric Induction ◽

Magnesium Salt ◽

Chiral Auxiliaries ◽

Pyridine Series ◽

Methyl Benzoylformate

New chiral auxiliaries derived from β -pinene: Their use in the asymmetric reduction of β-keto-esters

Tetrahedron Asymmetry ◽

10.1016/s0957-4166(00)82117-5 ◽

1991 ◽

Vol 2 (5) ◽

pp. 353-356 ◽

Cited By ~ 13

Author(s):

Mário Luiz Vasconcellos ◽

Jean d'Angelo ◽

Didier Desmaele ◽

Paulo R.R. Costa ◽

Dominique Potin

Keyword(s):

Asymmetric Reduction ◽

Chiral Auxiliaries ◽

Novel Camphor-Derived Chiral Auxiliaries: Significant Solvent and Additive Effects on Asymmetric Reduction of Chiral α-Keto Esters

The Journal of Organic Chemistry ◽

10.1021/jo9902188 ◽

1999 ◽

Vol 64 (19) ◽

pp. 6993-6998 ◽

Cited By ~ 33

Author(s):

Ying-Yuan Chu ◽

Chia-Sheng Yu ◽

Chiou-Juy Chen ◽

Kung-Shuo Yang ◽

Jung-Chaing Lain ◽

...

Keyword(s):

Asymmetric Reduction ◽

Additive Effects ◽

Chiral Auxiliaries ◽

ChemInform Abstract: The Preparation and Absolute Configuration of the Optically Active Forms of the Diastereoisomers of 2-(1-Phenylethyl)amino-1-phenylethanol and Their Use as Chiral Auxiliaries in the Asymmetric Reduction of Acetophenone with Modified L

ChemInform ◽

10.1002/chin.198729106 ◽

1987 ◽

Vol 18 (29) ◽

Author(s):

S. W. GARRY ◽

D. G. NEILSON

Keyword(s):

Absolute Configuration ◽

Asymmetric Reduction ◽

Optically Active ◽

The preparation and absolute configuration of the optically active forms of the diastereoisomers of 2-(1-phenylethyl)amino-1-phenylethanol and their use as chiral auxiliaries in the asymmetric reduction of acetophenone with modified lithium aluminium hydrides

Journal of the Chemical Society Perkin Transactions 1 ◽

10.1039/p19870000601 ◽

1987 ◽

pp. 601 ◽

Cited By ~ 16

Author(s):

Scott W. Garry ◽

Douglas G. Neilson

Keyword(s):

Absolute Configuration ◽

Asymmetric Reduction ◽

Optically Active ◽

Chiral Auxiliaries ◽

Lithium Aluminium

Oxadiazinones as chiral auxiliaries: Asymmetric conjugate addition reactions with Ephedra based oxadiazinones

10.1021/scimeetings.0c01411 ◽

2020 ◽

Author(s):

Fatima Olayemi Obe ◽

Shawn Hitchcock

Keyword(s):

Conjugate Addition ◽

Addition Reactions ◽