Stereoselective synthesis of endo-7-halo-3-oxo-2-azabicyclo[4.1.0]heptanes by reductive hydrodehalogenation of gem-dihalocyclopropanes

Current Organic Chemistry

Volumn 15, Issue 8, 2011, Pages 1230-1235

  Joseph, Jomy K ^a   Singhal, Sweety ^a   Jain, Suman L ^a   Sain, Bir ^a  

^a CSIR INDIAN INSTITUTE OF PETROLEUM   (India)

Author keywords

Cyclopropane derivatives; Heterocyclic compound; Monohydrodehalogenation; Reduction; Stereoselective synthesis

Indexed keywords

ISOMERS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; STEREOSELECTIVITY; SYNTHESIS (CHEMICAL);

% REDUCTIONS; COUPLING CONSTANTS; CYCLOPROPANE DERIVATIVE; HETEROCYCLIC COMPOUND; HIGHER YIELD; HOMONUCLEAR; HYDRO-DEHALOGENATION; METALLICS; MONOHYDRODEHALOGENATION; STEREOSELECTIVE SYNTHESIS;

HEPTANE;

EID: 79953308873     PISSN: 13852728     EISSN: None     Source Type: Journal    
DOI: 10.2174/138527211795203059     Document Type: Article

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