Efficient proline-catalyzed Michael additions of unmodified ketones to nitro olefins.
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Asymmetric Catalysis Special Feature Part II: New mechanistic studies on the proline-catalyzed aldol reactionRecent developments in asymmetric multicomponent reactions.Cinchona-based primary amine catalysis in the asymmetric functionalization of carbonyl compounds.Organocatalytic enantioselective desymmetrisation.Recent Advances in Asymmetric Organocatalyzed Conjugate Additions to Nitroalkenes.Stereospecific synthesis of conformationally constrained gamma-amino acids: new foldamer building blocks that support helical secondary structure.Organocatalyzed asymmetric Michael reaction of β-aryl-α-ketophosphonates and nitroalkenes.Synthesis, anticholinesterase and antioxidant potentials of ketoesters derivatives of succinimides: a possible role in the management of Alzheimer's.Synthesis of Prolinal Dithioacetals as Catalysts for the Highly Stereoselective Michael Addition of Ketones and Aldehydes to beta-Nitrostyrenes.The Cyanation of Prochiral Aldehydes with Chiral Copper Complexes of R-(+)/S-(-) -α-Ethylphenyl Amine in Methanol.Synthesis of new pyrrolidine-based organocatalysts and study of their use in the asymmetric Michael addition of aldehydes to nitroolefinsEnantioselective organocatalytic Michael addition of aldehydes to nitroethylene: efficient access to gamma2-amino acids.(2R,4R)-2-Hydr-oxy-4-(2-methoxy-phen-yl)bicyclo-[3.3.1]nonan-9-one.A highly efficient access to enantiopure tetrahydropyridines: dual-organocatalyst-promoted asymmetric cascade reaction.Peptide-catalyzed stereoselective conjugate addition reactions generating all-carbon quaternary stereogenic centers.Organocatalyzed stereospecific C-C bond formation of β-lactams.Michael addition of carbonyl compounds to nitroolefins under the catalysis of new pyrrolidine-based bifunctional organocatalysts.Catalytic peptide assemblies.Catalysis of Michael Additions by Covalently Modified G-Quadruplex DNA.The Diarylprolinol Silyl Ethers: Ten Years After.Mechanism of diphenylprolinol silyl ether catalyzed Michael addition revisited--but still controversial.The aminocyclodextrin/Pd(OAc)2 complex as an efficient catalyst for the Mizoroki-Heck cross-coupling reaction.Asymmetric Michael reaction catalyzed by proline lithium salt: efficient synthesis of L-proline and isoindoloisoquinolinone derivatives.Enantioselective Michael Addition ReactionsStereoselectivity through a network of non-classical CH weak interactions: a prospective study of a bicyclic organocatalytic scaffoldOptically Active α-Phenylethylamine as Efficient Organocatalyst in the Solvent-free Reactions Between 2,3-Butanedione and Conjugated NitroolefinsPolymer-Supported Enantioselective Bifunctional Catalysts for Nitro-Michael Addition of Ketones and AldehydesRigorous Conformational Analysis of Pyrrolidine Enamines with Relevance to OrganocatalysisStoichiometric Reactions of Enamines Derived from Diphenylprolinol Silyl Ethers with Nitro Olefins and Lessons for the Corresponding Organocatalytic Conversions - a SurveySolid-Phase Organic Synthesis and Catalysis: Some Recent Strategies Using Alumina, Silica, and Polyionic ResinsOrganocatalysis: Key Trends in Green Synthetic Chemistry, Challenges, Scope towards Heterogenization, and Importance from Research and Industrial Point of ViewControl of four stereocentres in a triple cascade organocatalytic reactionStructural insight into the aggregation of l-prolyl dipeptides and its effect on organocatalytic performance
P2860
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P2860
Efficient proline-catalyzed Michael additions of unmodified ketones to nitro olefins.
description
2001 nî lūn-bûn
@nan
2001 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Efficient proline-catalyzed Michael additions of unmodified ketones to nitro olefins.
@ast
Efficient proline-catalyzed Michael additions of unmodified ketones to nitro olefins.
@en
Efficient proline-catalyzed Michael additions of unmodified ketones to nitro olefins.
@nl
type
label
Efficient proline-catalyzed Michael additions of unmodified ketones to nitro olefins.
@ast
Efficient proline-catalyzed Michael additions of unmodified ketones to nitro olefins.
@en
Efficient proline-catalyzed Michael additions of unmodified ketones to nitro olefins.
@nl
prefLabel
Efficient proline-catalyzed Michael additions of unmodified ketones to nitro olefins.
@ast
Efficient proline-catalyzed Michael additions of unmodified ketones to nitro olefins.
@en
Efficient proline-catalyzed Michael additions of unmodified ketones to nitro olefins.
@nl
P2093
P356
P1433
P1476
Efficient proline-catalyzed Michael additions of unmodified ketones to nitro olefins.
@en
P2093
P304
P356
10.1021/OL015799D
P407
P577
2001-08-01T00:00:00Z