Stereoselective synthesis of enantiopure γ-aminoalcohols by reduction of chiral β-enaminoketones

Tetrahedron Asymmetry

Volumn 17, Issue 8, 2006, Pages 1308-1317

  Cimarelli, Cristina ^a   Giuli, Sandra ^a   Palmieri, Gianni ^a  

^a Dipartimento di Scienze Chimiche   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ACETIC ACID; AMINOALCOHOL; GAMMA AMINOALCOHOL DERIVATIVE; KETONE DERIVATIVE; SODIUM BOROHYDRIDE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CHIRALITY; CRYSTAL STRUCTURE; CYCLIZATION; DRUG CONFORMATION; DRUG IDENTIFICATION; DRUG SYNTHESIS; MOLECULAR MODEL; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; X RAY ANALYSIS;

EID: 33646837847     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2006.04.009     Document Type: Article

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32. 25NO Unit cell parameters: a 7.3524(13), b 28.645(5), c 8.4467(15), beta 100.635(2), space group P21) have been deposited with the Cambridge Crystallographic Data Center as supplementary material with the deposition number CCDC 288236. This data can be obtained, free of charge via http://www.ccdc.cam.ac.uk/conts/retrieving.html.