Asymmetric cross-dehydrogenative coupling enabled by the design and application of chiral triazole-containing phosphoric acids.
about
Influence of the substitution and conformation of C--H-bond-based bis-triazole acceptors in anion-binding catalysis.Organic chemistry. A data-intensive approach to mechanistic elucidation applied to chiral anion catalysis.Enantiodivergent Fluorination of Allylic Alcohols: Data Set Design Reveals Structural Interplay between Achiral Directing Group and Chiral Anion.An in situ directing group strategy for chiral anion phase-transfer fluorination of allylic alcoholsEnantioselective 1,1-arylborylation of alkenes: merging chiral anion phase transfer with Pd catalysis.A Nucleophilic Strategy for Enantioselective Intermolecular α-Amination: Access to Enantioenriched α-Arylamino Ketones.1,2,3,-Triazole-Based Catalysts: From Metal- to Supramolecular Organic Catalysis.Chiral counteranion strategy for asymmetric oxidative C(sp³)-H/C(sp³)-H coupling: enantioselective α-allylation of aldehydes with terminal alkenes.A Late Stage Strategy for the Functionalization of Triazolium-based NHC catalysts.Biomimetic Approach to the Catalytic Enantioselective Synthesis of FlavonoidsCross-dehydrogenative coupling and oxidative-amination reactions of ethers and alcohols with aromatics and heteroaromatics.Pursuit of Noncovalent Interactions for Strategic Site-Selective CatalysisChiral anion phase transfer of aryldiazonium cations: an enantioselective synthesis of C3-diazenated pyrroloindolines.Multidimensional Correlations in Asymmetric Catalysis through Parameterization of Uncatalyzed Transition States.Enantioselective Synthesis of N,S-Acetals by an Oxidative Pummerer-Type Transformation using Phase-Transfer Catalysis.Asymmetric fluorinative dearomatization of tryptamine derivatives.An Enantioselective Bidentate Auxiliary Directed Palladium-Catalyzed Benzylic C-H Arylation of Amines Using a BINOL Phosphate Ligand.Stacking and Electrostatic Interactions Drive the Stereoselectivity of Silylium-Ion Asymmetric Counteranion-Directed Catalysis.Visible-Light-Promoted Asymmetric Cross-Dehydrogenative Coupling of Tertiary Amines to Ketones by Synergistic Multiple Catalysis.Enantioselective Synthesis of Pyrroloindolines via Noncovalent Stabilization of Indole Radical Cations and Applications to the Synthesis of Alkaloid Natural Products.The first catalytic asymmetric thioacetalization by chiral phosphoric acid catalysis.Oxidative C-H functionalization of N-carbamoyl 1,2-dihydroquinolines.A practical oxidative C-H functionalization of N-carbamoyl tetrahydro-β-carbolines with diverse potassium trifluoroborates.Catalytic Enantioselective Assembly of Homoallylic Alcohols from Dienes, Aryldiazonium Salts, and Aldehydes.Catalytic enantioselective oxidative cross-coupling of benzylic ethers with aldehydes.Catalytic amounts of triarylaminium salt initiated aerobic oxidative coupling of N-aryl tetrahydroisoquinolines.Selective carboxylation of reactive benzylic C–H bonds by a hypervalent iodine(III)/inorganic bromide oxidation system.Enantioselective and diastereoselective azo-coupling/iminium-cyclizations: a unified strategy for the total syntheses of (-)-psychotriasine and (+)-pestalazine B.
P2860
Q30833949-9523A146-1389-4286-944B-B0B9ED0AF3B1Q30892012-FFBA503C-8493-4A56-99DC-DAA255CB1249Q31056932-6FDB889F-D10B-4B42-9B46-0190EF2B134CQ34282632-662616B9-4A28-4C9E-B6A9-24FB70C253CCQ36041380-FA54BB90-0D52-4937-890D-09FB781105EEQ37495203-6B4A722D-B64B-48AB-81AC-610D9B38C7A7Q38989386-D4CEE150-9931-4F98-8E40-5263F17D531CQ39129603-A0845651-E2B6-4207-B8FF-9A93398BA5A2Q40267727-C882E717-EAE3-4D8E-BFF0-ACC7A666DFB5Q41962241-4D9CE2DC-D84C-4AEA-9A7E-9945D7706849Q42130713-627CD796-E13B-4428-8BEA-6616FF09D297Q42378791-1A1FE557-FAD9-4BB9-B491-100F362AC4A9Q42672477-EAA3BD44-5965-48E1-93BF-37A6E92280CFQ45938050-5DC2CF98-C198-4235-A211-281B86F02DC9Q46676060-CDAFFA68-68D6-4BFC-966C-8BEAF6FD5B94Q48200980-BA121537-28D1-4308-8895-8AE79944FBD0Q48215023-0A0203C0-2020-478F-9A92-229B60900EC2Q48217323-59B0D3A5-C322-4D01-ADEC-C248BC5E649BQ48224035-7CC40910-4C1C-4DB1-B402-1307DEBFB4A9Q50064646-BCE87445-DC59-4FDB-B795-8BF39F2E938FQ50232975-9FE984FF-7445-4900-8B02-4650976F55CFQ50238427-ABCE849B-FC91-4D47-9F2C-69D0DEA2D262Q51142880-D9F6D3E4-D886-4116-8662-E5F03AEFF6A2Q51490611-78372BB6-CBF5-471F-885A-61D9C9B86E3DQ51752675-6BD2D4B7-DD36-47E5-9D1E-BE7E790A76E9Q53580032-B58A8697-5AD1-431D-9238-B0B699FD6F9CQ55423411-568D527A-84DD-4AEE-BB02-8F2CDAD8B832Q55461620-0C5B3DF2-5A65-443D-A6A6-6F67FBCFA98B
P2860
Asymmetric cross-dehydrogenative coupling enabled by the design and application of chiral triazole-containing phosphoric acids.
description
2013 nî lūn-bûn
@nan
2013 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Asymmetric cross-dehydrogenati ...... e-containing phosphoric acids.
@ast
Asymmetric cross-dehydrogenati ...... e-containing phosphoric acids.
@en
type
label
Asymmetric cross-dehydrogenati ...... e-containing phosphoric acids.
@ast
Asymmetric cross-dehydrogenati ...... e-containing phosphoric acids.
@en
prefLabel
Asymmetric cross-dehydrogenati ...... e-containing phosphoric acids.
@ast
Asymmetric cross-dehydrogenati ...... e-containing phosphoric acids.
@en
P2860
P50
P356
P1476
Asymmetric cross-dehydrogenati ...... e-containing phosphoric acids.
@en
P2093
Jörg P Hehn
P2860
P304
14044-14047
P356
10.1021/JA407410B
P407
P577
2013-09-11T00:00:00Z