2004
DOI: 10.1007/s10593-005-0066-y
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Regioselectivity of the interaction of (1S,2S)-2-amino-1-(4-nitrophenyl)-1,3-propanediol with some symmetrical ketones

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Cited by 2 publications
(1 citation statement)
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“…In most case, the product is a mixture (more than one structural isomer) [43]. Recently, Shan and coworkers reported that condensations of (1S,2S)-ANP with cyclohexanone, acetone, butanone, and pentan-3-one in toluene or xylene by azeotropic distillation in the absence of catalyst afforded almost quantitatively 1,2-cyclocondensation derivatives via a highly efficient chemoselectivity [44].…”
Section: Applications In Condensation Reactionsmentioning
confidence: 99%
“…In most case, the product is a mixture (more than one structural isomer) [43]. Recently, Shan and coworkers reported that condensations of (1S,2S)-ANP with cyclohexanone, acetone, butanone, and pentan-3-one in toluene or xylene by azeotropic distillation in the absence of catalyst afforded almost quantitatively 1,2-cyclocondensation derivatives via a highly efficient chemoselectivity [44].…”
Section: Applications In Condensation Reactionsmentioning
confidence: 99%