Optically active N-1-phenylethyl derivatives of (1R)-2-amino-1-phenylethanol as chiral auxiliaries in the enantioselective addition of diethylzinc to arylaldehydes

Tetrahedron: Asymmetry

Volumn 6, Issue 3, 1995, Pages 739-744

  Iuliano, Anna ^a   Pini, Dario ^a   Salvadori, Piero ^a  

^a UNIVERSITY OF PISA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ALKANOL;

ARTICLE; DRUG SYNTHESIS; ENANTIOMER; METHODOLOGY; PRIORITY JOURNAL; REACTION ANALYSIS; STEREOCHEMISTRY;

EID: 0028967003     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/0957-4166(95)00069-2     Document Type: Article

References (14)

1. Asymmetric Synthesis Utilizing External Chiral Ligands
2. Enantioselective Addition of Organometallic Reagents to Carbonyl Compounds: Chirality Transfer, Multiplication, and Amplification
3. 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
4. Chiral high-pressure liquid chromatographic stationary phases. 3. General resolution of arylalkylcarbinols