Enantioselective syntheses of morpholines and their homologues via S N2-type ring opening of aziridines and azetidines with haloalcohols

Journal of Organic Chemistry

Volumn 74, Issue 18, 2009, Pages 7013-7022

  Ghorai, Manas K ^a   Shukla, Dipti ^a   Das, Kalpataru ^a  

^a INDIAN INSTITUTE OF TECHNOLOGY KANPUR   (India)

Author keywords

[No Author keywords available]

Indexed keywords

AZETIDINES; AZIRIDINES; CHEMICAL EQUATIONS; ENANTIOSELECTIVE SYNTHESIS; HIGH YIELD; LEWIS ACID; MORPHOLINES; RING CLOSURES; RING OPENING; STEREO-SELECTIVE;

AMINES; ENANTIOSELECTIVITY;

CHEMICAL REACTIONS;

AMINE; ANTIDEPRESSANT AGENT; ANTIDIABETIC AGENT; ANTIOBESITY AGENT; APREPITANT; AZETIDINE DERIVATIVE; AZIRIDINE DERIVATIVE; BATRACHOTOXIN; HALOALCOHOL; HETEROCYCLIC COMPOUND; LEWIS ACID; MORPHOLINE DERIVATIVE; NATURAL PRODUCT; REBOXETINE;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL REACTION; CHEMICAL STRUCTURE; CHEMOTHERAPY INDUCED EMESIS; CHIRAL CHROMATOGRAPHY; CYCLIZATION; ELECTROSPRAY MASS SPECTROMETRY; ENANTIOSELECTIVITY; HALOGENATION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; PROTON NUCLEAR MAGNETIC RESONANCE; RING OPENING; STEREOCHEMISTRY; SYNTHESIS; X RAY CRYSTALLOGRAPHY;

ALCOHOLS; AMINES; AZETIDINES; AZIRIDINES; HYDROCARBONS, HALOGENATED; MORPHOLINES; STEREOISOMERISM;

EID: 70249140626     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo901297d     Document Type: Article

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