Dioxindole in asymmetric catalytic synthesis: direct access to 3-substituted 3-hydroxy-2-oxindoles via 1,4-additions to nitroalkenes.

Dioxindole in asymmetric catalytic synthesis: direct access to 3-substituted 3-hydroxy-2-oxindoles via 1,4-additions to nitroalkenes.

Item
http://www.wikidata.org/entity/Q34256647
Bifunctional primary amine-thioureas in asymmetric organocatalysis.Organocatalyzed asymmetric Michael reaction of β-aryl-α-ketophosphonates and nitroalkenes.An organocatalytic asymmetric sequential allylic alkylation-cyclization of Morita-Baylis-Hillman carbonates and 3-hydroxyoxindoles.Metal-free diastereoselective construction of bridged ketal spirooxindoles via a Michael addition-inspired sequence.Enantioselective synthesis of spiro γ-butyrolactones by N-heterocyclic carbene (NHC)-catalyzed formal [3 + 2] annulation of enals with 3-hydroxy oxindoles.A DBU-catalyzed Michael-Pinner-isomerization cascade reaction of 3-hydroxyoxindoles with isatylidene malononitriles: access to highly functionalized bispirooxindoles containing a fully substituted dihydrofuran motif.Sequential Au(i)/chiral tertiary amine catalysis: a tandem C-H functionalization of anisoles or a thiophene/asymmetric Michael addition sequence to quaternary oxindoles.Highly enantioselective Michael addition of 3-arylthio- and 3-alkylthiooxindoles to nitroolefins catalyzed by a simple cinchona alkaloid derived phosphoramide.Organocatalytic asymmetric synthesis of 3,3-disubstituted oxindoles featuring two heteroatoms at the C3 position.Transition-metal-free aerobic oxidative cleavage of C-C bonds in α-hydroxy ketones and mechanistic insight to the reaction pathway.Organocatalytic asymmetric Michael addition of 3-substituted oxindoles to α,β-unsaturated acyl phosphonates for the synthesis of 3,3'-disubstituted oxindoles with chiral squaramides.3-Pyrrolyl-oxindoles as efficient nucleophiles for organocatalytic asymmetric synthesis of structurally diverse 3,3'-disubstituted oxindole derivatives.From racemic precursors to fully stereocontrolled products: one-pot synthesis of chiral α-amino lactones and lactams.
P2860

Dioxindole in asymmetric catalytic synthesis: direct access to 3-substituted 3-hydroxy-2-oxindoles via 1,4-additions to nitroalkenes.

Item
http://www.wikidata.org/entity/Q34256647
description
2012 nî lūn-bûn
@nan
2012 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Dioxindole in asymmetric catal ...... 1,4-additions to nitroalkenes.
@ast
Dioxindole in asymmetric catal ...... 1,4-additions to nitroalkenes.
@en
Dioxindole in asymmetric catal ...... 1,4-additions to nitroalkenes.
@nl
type
label
Dioxindole in asymmetric catal ...... 1,4-additions to nitroalkenes.
@ast
Dioxindole in asymmetric catal ...... 1,4-additions to nitroalkenes.
@en
Dioxindole in asymmetric catal ...... 1,4-additions to nitroalkenes.
@nl
prefLabel
Dioxindole in asymmetric catal ...... 1,4-additions to nitroalkenes.
@ast
Dioxindole in asymmetric catal ...... 1,4-additions to nitroalkenes.
@en
Dioxindole in asymmetric catal ...... 1,4-additions to nitroalkenes.
@nl
P1433
P1476
P2093
P2860
P304
P31
P356
P407
P433
P478
P50
P577
P698
P356
P1433
P1476
Dioxindole in asymmetric catal ...... 1,4-additions to nitroalkenes
@en
P2093
P2860
P304
P31
P356
P407
P433
P478
P50
P577
P698