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Published in 2022 at "Chemical record"
DOI: 10.1002/tcr.202200159
Abstract: The aldol reaction is one of the most important carbon-carbon bond-forming reactions in organic chemistry. Asymmetric direct cross-aldol reaction of two different aldehydes has been regarded as a difficult reaction because of the side reactions… read more here.
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Published in 2018 at "Catalysis Letters"
DOI: 10.1007/s10562-018-2421-5
Abstract: A series of immobilized bipyridine-proline based on mesoporous silica with different structures were synthesized via grafting followed by coordination method. All catalysts were used in asymmetric aldol reaction of cyclohexanone with 4-nitrobenzaldehyde, and their catalytic… read more here.
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Published in 2020 at "Catalysis Letters"
DOI: 10.1007/s10562-020-03369-8
Abstract: Abstract A novel helical poly(phenyl isocyanide) bearing Boc protected l -proline pendants (poly- 1 m ) was designed and synthesized. Removed the protecting Boc groups on the l -proline pendants led to the formation of… read more here.
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Published in 2017 at "Russian Chemical Bulletin"
DOI: 10.1007/s11172-017-1730-y
Abstract: Carane-derived β-amino alcohols with amino and hydroxy groups at positions 3 and 4 differing in their mutual arrangement and configuration were synthesized. Their application as organocatalysts in the asymmetric aldol reaction of isatin with acetone… read more here.
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Published in 2017 at "Journal of Chemical Sciences"
DOI: 10.1007/s12039-017-1237-y
Abstract: AbstractA new class of organocatalysts involving a primary amine as the only functional group is developed for catalytic asymmetric aldol reaction of cyclohexanone/cyclopentanone with various aryl aldehydes in the presence of benzoic acid as an… read more here.
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Published in 2021 at "Journal of Molecular Structure"
DOI: 10.1016/j.molstruc.2021.130650
Abstract: Abstract Aldol reaction is a carbon-carbon bond forming chemical reaction for synthesis of β-hydroxy carbonyl compounds. In the current research work, we have synthesizedβ-hydroxy carbonyl compounds i.e 2-(hydroxy(4-nitrophenyl)methyl)cyclohexan-1-one (1) 2-(hydroxy(o-tolyl)methyl)cyclohexan-1-one (2) using base mediated aldol… read more here.
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Published in 2017 at "Tetrahedron"
DOI: 10.1016/j.tet.2017.03.093
Abstract: A bstract A highly convergent total synthesis of (+)-methynolide, based on two types of stereoselective aldol reaction, was achieved. The C1-C8 and C9-C11 fragments of (+)-methynolide were prepared by a vinylogous Mukaiyama aldol reaction using… read more here.
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Published in 2019 at "Tetrahedron"
DOI: 10.1016/j.tet.2018.11.041
Abstract: Abstract A copper(I)-catalyzed asymmetric borylative aldol reaction of 5,6-dihydro-2H-pyran-2-one and simple ketones (including aromatic ketones and an aliphatic ketone) was disclosed, which afforded a series of chiral diols after an oxidative work-up in moderate yields… read more here.
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Published in 2020 at "Tetrahedron"
DOI: 10.1016/j.tet.2019.130901
Abstract: Abstract The discovery and development of the vinylogous aldol reaction of N-sulfinyl metallodienamines with aldehydes and ketones is described. The diastereoselectivity of the reaction, first reported in 2017 as a key step in the total… read more here.
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Published in 2020 at "Organic letters"
DOI: 10.1021/acs.orglett.0c02816
Abstract: An oxetane intermediate during a direct aldol reaction was trapped with an internal aryl group to yield trans-tetraline products. The contribution of the oxetane intermediate was confirmed by 18O-isotope labeling experiments. read more here.
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Published in 2021 at "Organic letters"
DOI: 10.1021/acs.orglett.1c02196
Abstract: Substituted 9-methyldecalin derivatives containing an all carbon quaternary chiral center were synthesized with excellent enantioselectivity via an organocatalyst-mediated domino reaction. The first reaction is a diphenylprolinol silyl ether-mediated Michael reaction, and the second reaction is… read more here.