2009
DOI: 10.1039/b906684e
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Catalyst-free aldol condensation of ketones and isatins under mild reaction conditions in DMF with molecular sieves 4 Å as additive

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Cited by 46 publications
(19 citation statements)
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References 54 publications
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“…Chen et al (2009) investigated the effects of heavy metals and reported a correlation of Ni and V with cardiovascular mortality and morbidity. An extended study over six counties in California showed that Cu, K, Zn and Ti in PM 2.5 were related to multiple mortality categories, and especially to cardiovascular deaths (Ostro et al, 2007).…”
Section: Particulate Matter and Healthmentioning
confidence: 99%
“…Chen et al (2009) investigated the effects of heavy metals and reported a correlation of Ni and V with cardiovascular mortality and morbidity. An extended study over six counties in California showed that Cu, K, Zn and Ti in PM 2.5 were related to multiple mortality categories, and especially to cardiovascular deaths (Ostro et al, 2007).…”
Section: Particulate Matter and Healthmentioning
confidence: 99%
“…Although the water-soluble fraction of OA emitted by wood combustion can absorb light in the visible and ultraviolet region of the spectra, its overall absorption effect is rela-tively small but could be relevant over bright surfaces (Chen et al, 2010).…”
Section: Wood Combustionmentioning
confidence: 99%
“…As already discussed in the previous paragraph, aerosol-cloud interactions are nonlinear and very variable with space and time; hence, they are very difficult to quantify using observations. Chen et al (2010) investigated the effect of the change in aerosol number concentration and CCN that would result from the reduction in carbonaceous aerosol emissions using a global model. The authors reduced the primary emissions of black and OC mass and number from either only fossil fuel combustion or from all primary carbonaceous sources (fossil fuel, domestic fuel and biomass burning).…”
Section: Light-absorbing Carbonmentioning
confidence: 99%
“…We envisioned that the realization of this concept would open new avenues to access the important oxindole framework containing a tetrasubstituted stereogenic center at C-3 of the oxindole. Therefore, on the basis of some successes in stereoablative reactions [8a, 9] and as a continuation of our investigations aimed at developing new strategies for the synthesis of structurally diverse 3,3-disubstituted oxindole derivatives, [10] we developed a new strategy for the enantioselective synthesis of 3-substituted 3-hydroxy-2-oxindoles through stereoablative hydroxylation of 3-halooxindoles with environmentally benign organocatalysts and by using oximes [11] as oxygen nucleophiles (Scheme 1). To the best of our knowledge, this represents the first example employing 3-substituted oxindoles as electrophilic partners for the generation of enantioenriched 3-substituted 3-hydroxy-2-oxindole derivatives.…”
mentioning
confidence: 99%