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The first examples of atropisomerism in a few N,N′-diaryl 2-iminothiazolines have been reported by some of us, without determination of the enantiomerization barriers, by a resolution of the enantiomers on cellulose triacetate stationary phase: Djafri, A.; Bouchekara, M.; Djafri, F.; Benachenhou, F. J. Soc. Alger. Chim., 1996, 6, 123-136.
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Ed.: Herz, W.; Falk, H.; Kirby, G.W.; Moore, R.E., Springer, Wien, New York
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For non-biaryl atropisomers: (a) Clayden J. Non-biaryl Atropisomers: New Classes of Chiral Reagents, Auxiliaries and Ligands? Ed.: Schmalz, H.-G. Organic Synthesis Highlights IV, 2000, 48-52. Wiley-VCH Verlag GmbH, Weinheim, Germany.
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Reference 1 gives examples of hydrolysis under severe conditions. We were not able to reproduce the results reported for non-ortho- substituted aryl iminothiazolines in: Sahu, B.; Dash, B. C.; Tripathy, H.; Mahapatra, G. N. Indian J. Appl. Chem. 1970, 33, 256-258.
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Viswanathan, K. V.; Raghavan, M.; Guha, P. C. J. Indian Inst. Sci. 1953, 35A, 251-258 (Chem. Abs., 48: 64,250).
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