2012
DOI: 10.1016/j.crci.2012.03.010
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Étude mécanistique et structurale des résines R/F

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Cited by 5 publications
(3 citation statements)
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“…The weight loss tends to decrease by 20%, especially for temperatures 50 °C and 100 °C and becomes practically constant at 110 °C. 33,34 We note two weight losses for samples E2 and E3 between four and five days after drying at 110 °C (Figs 1c and 1d). This weight loss is mainly due to the desorption of physisorbed water and residual organic precursors.…”
Section: Resultsmentioning
confidence: 94%
“…The weight loss tends to decrease by 20%, especially for temperatures 50 °C and 100 °C and becomes practically constant at 110 °C. 33,34 We note two weight losses for samples E2 and E3 between four and five days after drying at 110 °C (Figs 1c and 1d). This weight loss is mainly due to the desorption of physisorbed water and residual organic precursors.…”
Section: Resultsmentioning
confidence: 94%
“…Synthesis of the profluorescent nitroxide probe PN1 is depicted in Scheme 2. Michael addition of nitro compound 1 29 to vinyl ketone 2 30 was performed to afford γ-nitro ketone 3 in 64% yield using Triton B as a base. Reductive cyclization of 3 utilizing zinc powder as a reducing agent provided nitrone 4 in 91% yield.…”
Section: Resultsmentioning
confidence: 99%
“…Traditionally, good results are obtained in the presence of catalytic amount of Lewis acids such as ZrOCl 2 ⋅ 8H 2 O, [56] AlCl 3 /SiO 2 , [57] FeCl 3 / Montmorillonite K 10, [58] TiCl 2 (OTf)/SiO 2 [59] (Table 1, entries 13–16). Finally, the aza‐Michael addition of aniline to 5 a is successfully promoted by N‐heterocyclic carbene, [60] enzyme, [61] ionic liquids [62,63] or phase‐transfer catalyst [64] (Table 1, entries 17–21). When the reaction is performed under the same conditions in various solvents (including water) without a catalyst, the target adduct is isolated in low yields or does not formed at all (Table 1, entries 22–25).…”
Section: Aza‐michael Reactions Without a Catalystmentioning
confidence: 99%