Magnesium(II)-catalyzed asymmetric hetero-Diels-Alder reaction of Brassard's dienes with isatins.
about
Enantioselective magnesium-catalyzed transformations.NHC-catalyzed [4+2] cycloaddition reactions for the synthesis of 3'-spirocyclic oxindoles via a C-F bond cleavage protocol.A Tunable and Enantioselective Hetero-Diels-Alder Reaction Provides Access to Distinct Piperidinoyl Spirooxindoles.Chiral metal phosphate catalysis: highly asymmetric hetero-Diels–Alder reactionsReaction-Based Mechanistic Investigations of Asymmetric Hetero-Diels-Alder Reactions of Enones with Isatins Catalyzed by Amine-Based Three-Component Catalyst SystemsCatalytic asymmetric hetero-Diels–Alder reactions of enones with isatins to access functionalized spirooxindole tetrahydropyrans: scope, derivatization, and discovery of bioactives
P2860
Magnesium(II)-catalyzed asymmetric hetero-Diels-Alder reaction of Brassard's dienes with isatins.
description
2014 nî lūn-bûn
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2014年の論文
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2014年学术文章
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2014年学术文章
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2014年学术文章
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2014年学术文章
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2014年学术文章
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2014年學術文章
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name
Magnesium(II)-catalyzed asymme ...... rassard's dienes with isatins.
@en
type
label
Magnesium(II)-catalyzed asymme ...... rassard's dienes with isatins.
@en
prefLabel
Magnesium(II)-catalyzed asymme ...... rassard's dienes with isatins.
@en
P2093
P2860
P50
P356
P1476
Magnesium(II)-catalyzed asymme ...... rassard's dienes with isatins.
@en
P2093
Jianfeng Zheng
Jiannan Zhao
Yulong Kuang
P2860
P304
P356
10.1039/C3CC47800A
P407
P577
2014-01-01T00:00:00Z