Journal
CHEMISTRY-A EUROPEAN JOURNAL
Volume 21, Issue 13, Pages 4975-4987Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201405551
Keywords
azides; donor-acceptor systems; heterocycles; nitrogen heterocycles; nucleophilic substitution
Categories
Funding
- Russian Scientific Foundation [14-13-01178]
- Russian Foundation for Basic Research [12-03-00717-a]
- Russian Science Foundation [14-13-01178] Funding Source: Russian Science Foundation
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A general method for ring opening of various donor-acceptor cyclopropanes with the azide ion through an S(N)2-like reaction has been developed. This highly regioselective and stereospecific process proceeds through nucleophilic attack on the more-substituted C2 atom of a cyclopropane with complete inversion of configuration at this center. Results of DFT calculations support the S(N)2 mechanism and demonstrate good qualitative correlation between the relative experimental reactivity of cyclopropanes and the calculated energy barriers. The reaction provides a straightforward approach to a variety of polyfunctional azides in up to 91% yield. The high synthetic utility of these azides and the possibilities of their involvement in diversity-oriented synthesis were demonstrated by the developed multipath strategy of their transformations into five-, six-, and seven-membered N-heterocycles, as well as complex annulated compounds, including natural products and medicines such as (-)-nicotine and atorvastatin.
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