Stereochemistry of the oxidation of imines derived from substituted cyclohexanones: Axial vs equatorial attack and evidence for delivery by an adjacent hydroxyl group

Journal of Organic Chemistry

Volumn 65, Issue 17, 2000, Pages 5120-5126

  Wang, Yuguang ^a,b   Chackalamannil, Samuel ^a,b   Aubé, Jeffrey ^a  

^a UNIVERSITY OF KANSAS   (United States)

^b MERCK RESEARCH LABORATORIES   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BENZYL DERIVATIVE; BENZYLAMINE; CYCLOHEXANONE DERIVATIVE; HYDROXYL GROUP; IMINE; OXAZIRIDINE DERIVATIVE; OXIDIZING AGENT;

ARTICLE; CHEMICAL REACTION; CONFORMATION; DERIVATIZATION; NUCLEAR MAGNETIC RESONANCE; OXIDATION; STEREOCHEMISTRY;

CYCLOHEXANONES; HYDROXYL RADICAL; IMINES; MAGNETIC RESONANCE SPECTROSCOPY; MASS SPECTROMETRY; OXIDATION-REDUCTION; STEREOISOMERISM;

EID: 0034714403     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo991928g     Document Type: Article

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