Catalytic enantioselective O-nitrosocarbonyl aldol reaction of β-dicarbonyl compounds. - Wikidata - wikimedia - TriplyDB

Catalytic enantioselective O-nitrosocarbonyl aldol reaction of β-dicarbonyl compounds.

Catalytic enantioselective O-nitrosocarbonyl aldol reaction of β-dicarbonyl compounds.

http://www.wikidata.org/entity/Q41879385

about

Continuous flow of nitroso Diels-Alder reaction.Ten years of research in Chicago.Cross-dehydrogenative coupling for the intermolecular C-O bond formation.Iron complexes of tetramine ligands catalyse allylic hydroxyamination via a nitroso-ene mechanism.The electrophilic α-amination of α-alkyl-β-ketoesters with in situ generated nitrosoformates.The Mukaiyama aldol reaction of in situ generated nitrosocarbonyl compounds: selective C-N bond formation and N-O bond cleavage in one-pot for α-amination of ketones.Williamson Ether Synthesis with Phenols at a Tertiary Stereogenic Carbon: Formal Enantioselective Phenoxylation of β-Keto Esters.Merging aerobic oxidation and enamine catalysis in the asymmetric α-amination of β-ketocarbonyls using N-hydroxycarbamates as nitrogen sources.Iminoxyl Radical-Based Strategy for Intermolecular CO Bond Formation: Cross-Dehydrogenative Coupling of 1,3-Dicarbonyl Compounds with Oximes Oxidative CO Cross-Coupling of 1,3-Dicarbonyl Compounds and Their Heteroanalogues withN-Substituted Hydroxamic Acids andN-Hydroxyimides

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P2860

Catalytic enantioselective O-nitrosocarbonyl aldol reaction of β-dicarbonyl compounds.

http://www.wikidata.org/entity/Q41879385

description

2012 nî lūn-bûn

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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2012年论文

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2012年论文

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name

Catalytic enantioselective O-nitrosocarbonyl aldol reaction of β-dicarbonyl compounds.

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type

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Catalytic enantioselective O-nitrosocarbonyl aldol reaction of β-dicarbonyl compounds.

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prefLabel

Catalytic enantioselective O-nitrosocarbonyl aldol reaction of β-dicarbonyl compounds.

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P1433

Journal of the American Chemical Society

P1476

Catalytic enantioselective O-nitrosocarbonyl aldol reaction of β-dicarbonyl compounds

@en

P2093

Hisashi Yamamoto

http://www.w3.org/2001/XMLSchema#string

Kimberly A Griffin

http://www.w3.org/2001/XMLSchema#string

P2860

Chiral bis(oxazoline) copper(II) complexes: versatile catalysts for enantioselective cycloaddition, Aldol, Michael, and carbonyl ene reactions.

Recent applications of oxazoline-containing ligands in asymmetric catalysis.

The nitroso ene reaction: a regioselective and stereoselective allylic nitrogen functionalization of mechanistic delight and synthetic potential.

Expanding the scope of asymmetric electrophilic atom-transfer reactions: titanium- and ruthenium-catalyzed hydroxylation of beta-ketoesters.

The nitrosocarbonyl hetero-Diels-Alder reaction as a useful tool for organic syntheses.

Copper-catalyzed aerobic oxidation of hydroxamic acids leads to a mild and versatile acylnitroso ene reaction.

Lewis acid-catalyzed enantioselective hydroxylation reactions of oxindoles and beta-keto esters using DBFOX ligand.

Chiral Brønsted acid-catalyzed enantioselective alpha-hydroxylation of beta-dicarbonyl compounds.

The oxidation of some carcinogenic arylhydroxylamines to nitroso derivatives with manganese dioxide.

Which is the actual catalyst: chiral phosphoric Acid or chiral calcium phosphate?

P304

18566-18569

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P31

scholarly article

P356

10.1021/JA309311Z

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P433

45

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P478

134

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Mahiuddin Baidya

P577

2012-11-02T00:00:00Z

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P698

23106266

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P921

enantioselectivity

P932

3515642

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