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Review
. 2018 Jun 6:14:1349-1369.
doi: 10.3762/bjoc.14.114. eCollection 2018.

Synthesis of chiral 3-substituted 3-amino-2-oxindoles through enantioselective catalytic nucleophilic additions to isatin imines

Affiliations
Review

Synthesis of chiral 3-substituted 3-amino-2-oxindoles through enantioselective catalytic nucleophilic additions to isatin imines

Hélène Pellissier. Beilstein J Org Chem. .

Abstract

This review collects the recent developments in the synthesis of chiral 3-substituted 3-amino-2-oxindoles based on enantioselective catalytic nucleophilic additions to isatin imines published since the beginning of 2015.

Keywords: asymmetric synthesis; chiral 3-amino-2-oxindoles; chirality; isatin imines; nucleophilic addition.

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Figures

Scheme 1
Scheme 1
Mannich reaction of N-Boc-isatin imines with ethyl nitroacetate (2) catalyzed by a cinchona alkaloid followed by denitration and synthesis of AG-041R.
Scheme 2
Scheme 2
Mannich reaction of N-Boc-isatin imines with 1,3-dicarbonyl compounds catalyzed by a cinchona alkaloid-derived squaramide.
Scheme 3
Scheme 3
Mannich reaction of N-alkoxycarbonylisatin imines with acetylacetone catalyzed by a cinchona alkaloid-derived squaramide.
Scheme 4
Scheme 4
Mannich reaction of isatin-derived benzhydrylketimines with trimethylsiloxyfuran catalyzed by a phosphoric acid.
Scheme 5
Scheme 5
Mannich reaction of N-Boc-isatin imines with acetaldehyde catalyzed by a primary amine.
Scheme 6
Scheme 6
Mannich reaction of N-Cbz-isatin imines with aldehydes catalyzed by L-diphenylprolinol trimethylsilyl ether.
Scheme 7
Scheme 7
Addition of dimedone-derived enaminones to N-Boc-isatin imines catalyzed by a phosphoric acid.
Scheme 8
Scheme 8
Addition of hydroxyfuran-2-one-derived enaminones to N-Boc-isatin imines catalyzed by a phosphoric acid.
Scheme 9
Scheme 9
Zinc-catalyzed Mannich reaction of N-Boc-isatin imines with silyl ketene imines.
Scheme 10
Scheme 10
Tin-catalyzed Mannich reaction of N-arylisatin imines with an alkenyl trichloroacetate.
Scheme 11
Scheme 11
Aza-Morita–Baylis–Hillman reaction of N-Boc-isatin imines with acrolein catalyzed by β-isocupreidine.
Scheme 12
Scheme 12
Aza-Morita–Baylis–Hillman reaction of N-Boc-isatin imines with acrolein (35) catalyzed by α-isocupreine.
Scheme 13
Scheme 13
Aza-Morita–Baylis–Hillman reaction of N-Boc-isatin imines with maleimides catalyzed by β-isocupreidine.
Scheme 14
Scheme 14
Aza-Morita–Baylis–Hillman reaction of N-Boc-isatin imines with nitroolefins catalyzed by a cinchona alkaloid-derived thiourea.
Scheme 15
Scheme 15
Friedel–Crafts reactions of N-Boc-isatin imines with 1 and 2-naphthols catalyzed by a cinchona alkaloid-derived thiourea.
Scheme 16
Scheme 16
Friedel–Crafts reactions of N-alkoxycarbonyl-isatin imines with 1 and 2-naphthols catalyzed by a cinchona alkaloid-derived squaramide.
Scheme 17
Scheme 17
Friedel–Crafts reaction of N-Boc-isatin imines with 6-hydroxyquinolines catalyzed by a cinchona alkaloid-derived thiourea.
Scheme 18
Scheme 18
Aza-Henry reaction of N-Boc-isatin imines with nitromethane catalyzed by a bifunctional guanidine.
Scheme 19
Scheme 19
Domino addition/cyclization reaction of N-Boc-isatin imines with 1,4-dithiane-2,5-diol (53) catalyzed by a tertiary amine-squaramide.
Scheme 20
Scheme 20
Nickel-catalyzed additions of methanol and cumene hydroperoxide to N-Boc-isatin imines.
Scheme 21
Scheme 21
Palladium-catalyzed addition of arylboronic acids to N-tert-butylsulfonylisatin imines.

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References

    1. Jensen B S. CNS Drug Rev. 2002;8:353–360. doi: 10.1111/j.1527-3458.2002.tb00233.x. - DOI - PMC - PubMed
    1. Dounay A B, Overman L E. Chem Rev. 2003;103:2945–2964. doi: 10.1021/cr020039h. - DOI - PubMed
    1. Galliford C V, Scheidt K. Angew Chem, Int Ed. 2007;46:8748–8758. doi: 10.1002/anie.200701342. - DOI - PubMed
    1. Singh G S, D’hooghe M, De Kimpe N. Chem Rev. 2007;107:2080–2135. doi: 10.1021/cr0680033. - DOI - PubMed
    1. Singh G S, Desta Z Y. Chem Rev. 2012;112:6104–6155. doi: 10.1021/cr300135y. - DOI - PubMed

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