A highly efficient solvent-free asymmetric direct aldol reaction organocatalyzed by recoverable (S)-binam-L-prolinamides. ESI-MS evidence of the enamine-iminium formation.
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Enantiomeric separation of biaryl atropisomers using cyclofructan based chiral stationary phases.Catalytic Asymmetric Mannich Reactions with Fluorinated Aromatic Ketones: Efficient Access to Chiral β-Fluoroamines.The direct catalytic asymmetric aldol reaction.Fluorine & chirality: how to create a nonracemic stereogenic carbon-fluorine centre?Ball milling in organic synthesis: solutions and challenges.Enantioselective organocatalytic fluorination using organofluoro nucleophiles.Recent efforts directed to the development of more sustainable asymmetric organocatalysis.Mechanochemistry assisted asymmetric organocatalysis: A sustainable approach.Mechanochemical organic synthesis.β-Siloxy-α-haloketones through highly diastereoselective single and double mukaiyama aldol reactions.Mechanochemical synthesis of small organic molecules.Benign by design: catalyst-free in-water, on-water green chemical methodologies in organic synthesis.Organocatalyzed stereospecific C-C bond formation of β-lactams.An L-proline functionalized metallo-organic triangle as size-selective homogeneous catalyst for asymmetry catalyzing aldol reactions.New general synthesis of α-alkoxyketones via α'-alkylation, α-alkylation and α,α'-dialkylation of α-alkoxyketimines.Highly enantioselective kinetic resolution of axially chiral BINAM derivatives catalyzed by a Brønsted acid.Catalytic enantioselective difluoroalkylation of aldehydes.Preparation of Chiral Amino Esters by Asymmetric Phase-Transfer Catalyzed Alkylations of Schiff Bases in a Ball Mill
P2860
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P2860
A highly efficient solvent-free asymmetric direct aldol reaction organocatalyzed by recoverable (S)-binam-L-prolinamides. ESI-MS evidence of the enamine-iminium formation.
description
2008 nî lūn-bûn
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2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
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2008年學術文章
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name
A highly efficient solvent-fre ...... the enamine-iminium formation.
@en
A highly efficient solvent-fre ...... organocatalyzed by recoverable
@nl
type
label
A highly efficient solvent-fre ...... the enamine-iminium formation.
@en
A highly efficient solvent-fre ...... organocatalyzed by recoverable
@nl
prefLabel
A highly efficient solvent-fre ...... the enamine-iminium formation.
@en
A highly efficient solvent-fre ...... organocatalyzed by recoverable
@nl
P2093
P356
P1476
A highly efficient solvent-fre ...... the enamine-iminium formation.
@en
P2093
Carmen Nájera
Gabriela Guillena
Maria del Carmen Hita
Santiago F Viózquez
P304
P356
10.1021/JO800773Q
P407
P577
2008-07-04T00:00:00Z