An Efficient System For the Pd-Catalyzed Cross-Coupling of Amides and Aryl Chlorides. - Wikidata - awgldk - TriplyDB

An Efficient System For the Pd-Catalyzed Cross-Coupling of Amides and Aryl Chlorides.

An Efficient System For the Pd-Catalyzed Cross-Coupling of Amides and Aryl Chlorides.

http://www.wikidata.org/entity/Q34081003

about

Pd-catalyzed N-arylation of secondary acyclic amides: catalyst development, scope, and computational study Pd-catalyzed cross-coupling reactions of amides and aryl mesylates.Pd-catalyzed O-arylation of ethyl acetohydroximate: synthesis of O-arylhydroxylamines and substituted benzofurans.Palladium-catalyzed arylation of cyanamides.Dialkylbiaryl Phosphines in Pd-Catalyzed Amination: A User's Guide.A multiligand based Pd catalyst for C-N cross-coupling reactions.Pd-catalyzed conversion of aryl chlorides, triflates, and nonaflates to nitroaromatics Synthesis of unsymmetrical diarylureas via Pd-catalyzed C-N cross-coupling reactions.A new biarylphosphine ligand for the Pd-catalyzed synthesis of diaryl ethers under mild conditions.Palladium-catalyzed N-arylation of 2-aminothiazoles Evidence for in situ catalyst modification during the Pd-catalyzed conversion of aryl triflates to aryl fluorides.A bulky biaryl phosphine ligand allows for palladium-catalyzed amidation of five-membered heterocycles as electrophiles Palladium-catalyzed cross-coupling of aryl chlorides and triflates with sodium cyanate: a practical synthesis of unsymmetrical ureas.Palladium-catalyzed N-monoarylation of amidines and a one-pot synthesis of quinazoline derivatives.Investigating the dearomative rearrangement of biaryl phosphine-ligated Pd(II) complexes.An Improved Synthesis of BrettPhos and RockPhos-Type Biarylphosphine Ligands.Synthesis and application of palladium precatalysts that accommodate extremely bulky di-tert-butylphosphino biaryl ligands.Cascade palladium catalysis: a predictable and selectable regiocontrolled synthesis of N-arylbenzimidazoles.Pd-catalyzed nucleophilic fluorination of aryl bromides Palladium-catalyzed amination of unprotected five-membered heterocyclic bromides Metal-catalysed approaches to amide bond formation.Applications of Palladium-Catalyzed C-N Cross-Coupling Reactions.Palladium-catalyzed C-N and C-O bond formation of N-substituted 4-bromo-7-azaindoles with amides, amines, amino acid esters and phenols Ligand-controlled regiodivergent palladium-catalyzed decarboxylative allylation reaction to access α,α-difluoroketones.Pd-catalyzed C-N bond formation with heteroaromatic tosylates.Palladium-Mediated Arylation of Lysine in Unprotected Peptides.BippyPhos: a single ligand with unprecedented scope in the Buchwald-Hartwig amination of (hetero)aryl chlorides.Base-catalyzed synthesis of aryl amides from aryl azides and aldehydes.

P2860

Q33586499-5F5F2EAE-F6B2-4F22-978A-1599D6B81008 Q33870854-FADCF96A-89C9-46A7-9A99-95F5CC1E0BD3 Q34065855-68F218DA-690E-4378-975E-2651E1940BFF Q34238310-0B49B66B-18B4-456E-BAF1-ED56B9081941 Q34262474-3147F5D3-8DB5-419E-A68F-2557AF13382A Q34369527-727F1B10-2F02-4F6C-8C51-600B910D22A9 Q35001565-E2C1F32D-C112-434B-B178-1302A02EE5CC Q35080163-F259416A-85AC-4C40-97AF-F1BD98DEA337 Q35691917-07A43FBD-93CA-4154-9C68-732B2B9F83DB Q35871315-2871E091-F477-4175-9C26-DFAF78B73ED2 Q35967391-1788863D-03E5-4D91-83B1-5E65758E2C5A Q36124268-0D0C3F2B-0CF1-474A-88AB-820161897016 Q36320551-A7E7BF63-3116-4435-AAA9-56C47C4765A9 Q36360751-99F661C4-BDBB-48B7-9524-7A00ADBC2355 Q36489784-3C2CB3EB-E05B-4D17-BF19-53118C56F3E1 Q36713972-C682C97E-558B-46CA-A59F-64E215E42FFA Q37030381-84ABB28A-355A-4497-ADAC-9463515D32CA Q37419633-ED8AB21B-7113-480E-88FC-347F160CA184 Q37637811-11E77498-BEC1-4D56-A732-885EBE14CDC5 Q37697316-22A6244C-30A2-48CF-A93D-F289FCC57B03 Q37854482-44213246-7A30-4073-B3C6-439936105D19 Q38968855-980186BA-32C4-4BFA-8A8F-C262AE542B22 Q42373983-1777A0F3-C270-425E-9624-8C94CFD8BBA6 Q42696564-D70CBC4B-29B6-47BD-8B80-82485FA5A1BF Q43106298-22A56D17-CA90-4B39-BB9E-FDD4B8E1AECF Q52720422-2180A312-74C3-42F8-883A-C63B416BC203 Q54528959-9080D344-8874-48D7-B5D5-AD907D7B55F1 Q55258478-40749700-8531-46D9-9074-3B723431D89F

P2860

An Efficient System For the Pd-Catalyzed Cross-Coupling of Amides and Aryl Chlorides.

http://www.wikidata.org/entity/Q34081003

description

2009 nî lūn-bûn

@nan

2009 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2009年の論文

@ja

2009年論文

@yue

2009年論文

@zh-hant

2009年論文

@zh-hk

2009年論文

@zh-mo

2009年論文

@zh-tw

2009年论文

@wuu

name

An Efficient System For the Pd-Catalyzed Cross-Coupling of Amides and Aryl Chlorides.

@ast

An Efficient System For the Pd-Catalyzed Cross-Coupling of Amides and Aryl Chlorides.

@en

An Efficient System For the Pd-Catalyzed Cross-Coupling of Amides and Aryl Chlorides.

@nl

type

label

An Efficient System For the Pd-Catalyzed Cross-Coupling of Amides and Aryl Chlorides.

@ast

An Efficient System For the Pd-Catalyzed Cross-Coupling of Amides and Aryl Chlorides.

@en

An Efficient System For the Pd-Catalyzed Cross-Coupling of Amides and Aryl Chlorides.

@nl

prefLabel

An Efficient System For the Pd-Catalyzed Cross-Coupling of Amides and Aryl Chlorides.

@ast

An Efficient System For the Pd-Catalyzed Cross-Coupling of Amides and Aryl Chlorides.

@en

An Efficient System For the Pd-Catalyzed Cross-Coupling of Amides and Aryl Chlorides.

@nl

P1433

Q34081003-BA5633C6-A1A1-464E-94D6-876A6A995823

P1476

Q34081003-E6D7A7FE-81C3-42F8-BF82-91AC2B151B15

P2093

Q34081003-21A292A6-28BE-4E0A-86D3-F155A6170B6B

Q34081003-6AA2B413-C3D5-4947-9117-3D550CC069BE

Q34081003-B565A5F5-C355-4C9B-A7AC-874B5BD4DE08

Q34081003-FC86E258-CFCD-4BFB-A9B2-4B380428452A

P2860

Q34081003-02BB684A-0F8A-4D7B-BAEC-F519A7EE5DF2

Q34081003-147E1718-8A47-4E6E-9537-BD831ABD422B

Q34081003-1620DA69-EE71-445F-82EF-BCC6A95A45FF

Q34081003-2C04AE23-88C5-4166-81B8-AE6688EF30EF

Q34081003-31EC2454-3525-4D9A-801C-4073AD13F715

Q34081003-3904D303-B11D-4281-B6EC-0BD5542E4FAB

Q34081003-3B9C822B-858A-4992-8366-70F886B1A608

Q34081003-449E6410-B913-4167-8B69-219B0CD02547

Q34081003-5FCA2031-BD30-4B78-90AC-0AD4D993AF5A

Q34081003-86EBE193-6BD1-4761-A4FD-568A12A86939

P304

Q34081003-C399C7C7-1F3F-4985-91AA-69AF732EC824

P31

Q34081003-502AF974-4712-4477-9680-2A4FB1BFC38E

P356

Q34081003-5C8C399C-A6C6-4DF6-84E2-FA1FA6075CD5

P433

Q34081003-9F2DE8FE-8900-46ED-ADE3-508C239D6134

P478

Q34081003-947F30A2-D2D6-4E05-A06B-E22201F302DA

P577

Q34081003-E571A5D1-6F8D-4D4E-B7C1-10798BFBF064

P5875

Q34081003-7D0EE733-29A0-470A-9059-77338DC5820E

P698

Q34081003-B141E4BE-2ED9-44A3-B795-298FC60778E8

P932

Q34081003-C211D8FD-85BA-46B6-B3FB-E04C82C66719

P356

J.TET.2009.04.096

P1433

P1476

An Efficient System For the Pd-Catalyzed Cross-Coupling of Amides and Aryl Chlorides.

@en

P2093

Brett P Fors

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

Karin Dooleweerdt

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

Qingle Zeng

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

Stephen L Buchwald

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

P2860

Expanding Pd-catalyzed C-N bond-forming processes: the first amidation of aryl sulfonates, aqueous amination, and complementarity with Cu-catalyzed reactions

Modern Synthetic Methods for Copper-Mediated C(aryl)–O, C(aryl)–N, and C(aryl)–S Bond Formation

Biaryl Phosphane Ligands in Palladium-Catalyzed Amination

Monodentate Phosphines Provide Highly Active Catalysts for Pd-Catalyzed CN Bond-Forming Reactions of Heteroaromatic Halides/Amines and (H)N-Heterocycles

Water-mediated catalyst preactivation: an efficient protocol for C-N cross-coupling reactions.

Pd-catalyzed amidation of aryl chlorides using monodentate biaryl phosphine ligands: a kinetic, computational, and synthetic investigation.

N-amidation by copper-mediated cross-coupling of organostannanes or boronic acids with o-acetyl hydroxamic acids.

A highly active catalyst for Pd-catalyzed amination reactions: cross-coupling reactions using aryl mesylates and the highly selective monoarylation of primary amines using aryl chlorides.

Mechanistic studies on the copper-catalyzed N-arylation of amides.

Lewis acid acceleration of C-N bond-forming reductive elimination from heteroarylpalladium complexes and catalytic amidation of heteroaryl bromides.

P304

6576-6583

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

P31

scholarly article

P356

10.1016/J.TET.2009.04.096

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

P433

33

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

P478

65

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

P577

2009-08-01T00:00:00Z

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

P5875

45952336

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

P698

20740063

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

P932

2927134

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