Au(I)-catalyzed enantioselective 1,3-dipolar cycloadditions of münchnones with electron-deficient alkenes.
about
Novel three-component synthesis and antiproliferative properties of diversely functionalized pyrrolinesA Reactivity-Driven Approach to the Discovery and Development of Gold-Catalyzed Organic Reactions.Gold(I)-catalyzed diastereo- and enantioselective 1,3-dipolar cycloaddition and Mannich reactions of azlactones.Ligand effects in homogeneous Au catalysis.Oxazolones in organocatalysis, new tricks for an old reagent.Recent developments in gold-catalyzed cycloaddition reactions.Gold(I)-catalyzed enantioselective cycloaddition reactions.Chiral Brønsted acid from a cationic gold(I) complex: catalytic enantioselective protonation of silyl enol ethers of ketones.Enantioselective cycloaddition of münchnones onto [60]fullerene: organocatalysis versus metal catalysis.Chiral gold(I) vs chiral silver complexes as catalysts for the enantioselective synthesis of the second generation GSK-hepatitis C virus inhibitor.Azlactone Reaction Developments.Gold-Catalyzed Enantioselective Annulations.Enantioselective synthesis of cyclic carbamimidates via a three-component reaction of imines, terminal alkynes, and p-toluenesulfonylisocyanate using a monophosphine gold(I) catalyst().Synthesis of azepines by a gold-catalyzed intermolecular [4 + 3]-annulation.Synthetic scope and DFT analysis of the chiral binap-gold(I) complex-catalyzed 1,3-dipolar cycloaddition of azlactones with alkenes.Gold-catalyzed [3+3]-annulation of azomethine imines with propargyl esters.Atropisomeric [(diphosphine)Au2 Cl2 ] complexes and their catalytic activity towards asymmetric cycloisomerisation of 1,6-enynes.Asymmetric synthesis of medium-sized rings by intramolecular Au(I)-catalyzed cyclopropanation.Organocatalytic diastereo- and enantioselective 1,3-dipolar cycloaddition of azlactones and methyleneindolinones.Gold-catalyzed annulations of 2-alkynyl benzaldehydes with vinyl ethers: synthesis of dihydronaphthalene, isochromene, and bicyclo[2.2.2]octane derivatives.Catalytic asymmetric synthesis of a nitrogen heterocycle through stereocontrolled direct photoreaction from electronically excited state.Catalytic Asymmetric Inverse-Electron-Demand 1,3-Dipolar Cycloaddition of C,N-Cyclic Azomethine Imines with Azlactones: Access to Chiral Tricyclic Tetrahydroisoquinolines.Catalytic Asymmetric Cycloaddition of In Situ-Generated ortho-Quinone Methides and Azlactones by a Triple Brønsted Acid Activation Strategy.Asymmetric Michael Addition of Aldimino Esters with Chalcones Catalyzed by Silver/Xing-Phos: Mechanism-Oriented Divergent Synthesis of Chiral Pyrrolines.Organocatalytic enantioselective formal arylation of azlactones using quinones as the aromatic partner.Diastereoselective nucleophilic ring-opening reactions of 2,6-diazasemibullvalenes for the synthesis of diverse functionalized δ(1) -bipyrroline derivatives.Repurposing of oxazolone chemistry: gaining access to functionalized graphene nanosheets in a top-down approach from graphite.
P2860
Q33316600-4A5EF4DD-5F7F-4908-AA54-35EFB80142A7Q34377834-CFD1E6B8-2E8F-445B-99AE-DB31A9E8EE99Q34664654-F70ABB59-DEBC-4259-96B4-6592D1144271Q37225816-134DC09E-5496-4610-BAD5-D24C2A419B47Q37846197-0D108D3C-955B-4A7A-869A-59C5E55D24BFQ37931624-9B379CB3-0576-409D-B5F3-56F79F697C49Q38160845-F4548657-1B62-476E-B9AF-B976E3C3A50AQ38258517-30A0E2BC-A211-42AA-BCEE-F35039384DB6Q38276457-F8D889EE-9602-4118-832D-B65DE9C80C7EQ38365260-5B973092-4F18-4082-A582-0EC5C54BE363Q38849139-70EFF1AF-E949-4716-90B0-95F31E0D138CQ38977009-11DE8E35-6FF9-4F73-9990-53E5B21174A6Q41770732-0E8CD7B6-88E4-4AD8-AF24-B1FBAC2CBC93Q41858774-A757CF6A-388F-4A94-A538-EA5DE2CDEB4BQ42075052-FAC6F4E7-DD54-4048-9E60-A4E3CDD3FA8BQ42180491-20607BD3-F440-4A00-8D5F-1D8540E0FEC5Q42414639-8929A13A-C7CF-4E7C-B2F3-86C0A0306ABBQ43153910-B9D86080-1095-465F-8A5D-153DD7DB2423Q43447189-A14BECA3-DE92-4D80-8B72-88F2CE8A8F13Q43864271-D10FB3C9-AAED-4739-A27F-7E57F8392257Q47117872-66378E35-BB8B-450E-951E-491F6B49DFE4Q50854219-569676C2-92CF-49B9-8E56-A1CD7605267DQ50868672-E8D81F29-3D5E-4733-9DEF-7B3D91464B0AQ53087631-E8E15AEC-BADE-416B-AE9F-06C70909586DQ53464058-15409901-7430-410A-8E9A-033AAEC0AE99Q53513257-870F447C-9EE6-4589-81C1-978C0932EAC7Q55010595-4BE0AE38-9353-43F9-9B0C-CBE1453A3BFC
P2860
Au(I)-catalyzed enantioselective 1,3-dipolar cycloadditions of münchnones with electron-deficient alkenes.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年学术文章
@wuu
2007年学术文章
@zh
2007年学术文章
@zh-cn
2007年学术文章
@zh-hans
2007年学术文章
@zh-my
2007年学术文章
@zh-sg
2007年學術文章
@yue
2007年學術文章
@zh-hant
name
Au(I)-catalyzed enantioselecti ...... th electron-deficient alkenes.
@en
Au(I)-catalyzed enantioselecti ...... th electron-deficient alkenes.
@nl
type
label
Au(I)-catalyzed enantioselecti ...... th electron-deficient alkenes.
@en
Au(I)-catalyzed enantioselecti ...... th electron-deficient alkenes.
@nl
prefLabel
Au(I)-catalyzed enantioselecti ...... th electron-deficient alkenes.
@en
Au(I)-catalyzed enantioselecti ...... th electron-deficient alkenes.
@nl
P356
P1476
Au(I)-catalyzed enantioselecti ...... th electron-deficient alkenes.
@en
P2093
Asa D Melhado
Marco Luparia
P304
12638-12639
P356
10.1021/JA074824T
P407
P577
2007-09-28T00:00:00Z