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Published in 2024 at "Asian Journal of Organic Chemistry"
DOI: 10.1002/ajoc.202400422
Abstract: We report a convenient and diastereoselective copper‐catalyzed reductive alkynone aldol addition to aldehydes, with pinacolborane as stoichiometric reductant, that results in the generation of densely functionalized, trisubstituted (Z)‐enone products analogous to Morita‐Baylis‐Hillman adducts. We demonstrate…
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Keywords:
aldol;
practical access;
morita baylis;
baylis hillman ... See more keywords
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Published in 2021 at "Organic letters"
DOI: 10.1021/acs.orglett.1c00337
Abstract: N-Heterocyclic carbene-catalyzed tandem Stetter-aldol reaction of phthalaldehyde and α,β-unsaturated ketimines has been developed to afford functionalized naphthalen-1(2H)-one derivatives as the formal [4+2] annulation product. Interestingly, the reaction of aldimines led to the formation of isoquinoline…
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Keywords:
nhc mediated;
mediated stetter;
aldol;
aldol imino ... See more keywords
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Published in 2023 at "Synthetic Communications"
DOI: 10.1080/00397911.2023.2205593
Abstract: Abstract A proline-based, chiral bi-functional organocatalyst containing both pyrrolidine and oxadiazolone heterocycle, has been successfully applied for stereoselective aldol reactions. The replacement of polar -COOH group of proline with bioisostere oxadiazolone ring provides excellent solubility…
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Keywords:
pyrrolidine oxadiazolone;
condensation;
oxadiazolone conjugate;
organocatalyst ... See more keywords
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Published in 2019 at "Catalysts"
DOI: 10.3390/catal9050398
Abstract: A series of poly(2-oxazoline) (POX) derivatives bearing prolinamide pendants were designed as organocatalysts and evaluated in the direct asymmetric aldol reaction between aromatic aldehydes and cyclic ketones. The structural variation of the alkyl spacer connecting…
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Keywords:
aldol reaction;
bound;
aldol;
reaction ... See more keywords