Asymmetric direct α-alkylation of 2-oxindoles with Michler's hydrol catalyzed by bis-cinchona alkaloid-Brønsted acid via an SN1-type pathway.
about
Highly enantioselective Michael addition of 3-arylthio- and 3-alkylthiooxindoles to nitroolefins catalyzed by a simple cinchona alkaloid derived phosphoramide.3-Pyrrolyl-oxindoles as efficient nucleophiles for organocatalytic asymmetric synthesis of structurally diverse 3,3'-disubstituted oxindole derivatives.Highly enantioselective reaction of 2-oxindoles with (3-indolyl)methanols by cooperative Catalysis of a Lewis acid and organocatalyst
P2860
Asymmetric direct α-alkylation of 2-oxindoles with Michler's hydrol catalyzed by bis-cinchona alkaloid-Brønsted acid via an SN1-type pathway.
description
2013 nî lūn-bûn
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name
Asymmetric direct α-alkylation ...... acid via an SN1-type pathway.
@en
Asymmetric direct α-alkylation ...... acid via an SN1-type pathway.
@nl
type
label
Asymmetric direct α-alkylation ...... acid via an SN1-type pathway.
@en
Asymmetric direct α-alkylation ...... acid via an SN1-type pathway.
@nl
prefLabel
Asymmetric direct α-alkylation ...... acid via an SN1-type pathway.
@en
Asymmetric direct α-alkylation ...... acid via an SN1-type pathway.
@nl
P2093
P2860
P356
P1476
Asymmetric direct α-alkylation ...... acid via an SN1-type pathway.
@en
P2093
Nengjun Zhong
Yong-Jun Chen
P2860
P304
P356
10.1039/C3CC39012H
P407
P577
2013-02-01T00:00:00Z