Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/4370
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Type: Journal article
Title: Dipolar cycloaddition reactions of nitrilimines
Author: Dunstan, J.
Elsey, G.
Russell, R.
Savage, G.
Simpson, G.
Tiekink, E.
Citation: Australian Journal of Chemistry: an international journal for chemical science, 1998; 51(6):499-509
Publisher: C S I R O PUBLICATIONS
Issue Date: 1998
ISSN: 0004-9425
Statement of
Responsibility: 
James B. F. Dunstan, Gordon M. Elsey, Richard A. Russell, G. Paul Savage, Gregory W. Simpson and Edward R. T. Tiekink
Abstract: A series of γ-substituted α-methylidene-γ-butyrolactone derivatives underwent regiospecific 1,3-dipolar cycloaddition with N-methyl-C-phenylnitrilimine. These reactions proceeded regiospecifically and with high diastereoselectivity, generally favouring the anti diastereomer as determined by n.m.r. spectroscopy and semiempirical molecular orbital calculations. The assignment for one product was confirmed by X-ray crystallography. N-Methyl-C-phenylnitrilimine underwent regiospecific cycloaddition with a range of C=S-containing dipolarophiles. Substituted thioureas were generally unreactive as dipolarophiles, while 5-thio-substituted 1,3,4-thiadiazole-2(3H)-thiones underwent ready reaction to produce, rather than the expected cycloadducts, complex rearrangement products. The structure of one of these unusual products has been confirmed by X-ray crystallography. A series of disubstituted nitrilimines underwent regiospecific cycloaddition with thiobenzophenone; the structures of the products were confirmed by X-ray crystallography.
Rights: © CSIRO 1998
DOI: 10.1071/C97157
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