A facile regioselective ring opening of aziridines to haloamines using tetrabutylammonium halides in the presence of β-cyclodextrin in water

Tetrahedron Letters

Volumn 45, Issue 43, 2004, Pages 7995-7997

  Narender, M ^a   Surendra, K ^a   Krishnaveni, N Srilakshmi ^a   Reddy, M Somi ^a   Rao, K Rama ^a  

^a INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

Author keywords

Cyclodextrin; Aziridines; Haloamines; Tetrabutylammonium halide; Water

Indexed keywords

AZIRIDINE DERIVATIVE; BETA CYCLODEXTRIN; HALIDE; HALOAMINE; WATER;

ARTICLE; PH; RING OPENING; ROOM TEMPERATURE; STEREOCHEMISTRY;

EID: 4644359513     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.09.014     Document Type: Article

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31. 4), filtered and the solvent was removed under vacuum. The crude product was purified by silica gel column chromatography using ethyl acetate-hexane (2:8) as eluent