Regioselective formation of the quinazoline moiety on the upper rim of calix[4]arene as a route to inherently chiral systems
N-acyl aminocalix[4]arenes were cyclized with nitriles to afford the expected quinazolines only in the case of para-substituted series. This strategy represents a new route to inherently chiral calixarenes potentially useful as fluorescent receptors.
2012 ◽
Vol 48
(2)
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pp. 284-292
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2011 ◽
Vol 12
(1)
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pp. 429-455
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1994 ◽
Vol 19
(1-4)
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pp. 17-39
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