About: Synthesis and application of palladium precatalysts that accommodate extremely bulky di-tert-butylphosphino biaryl ligands

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scientific article published on 15 May 2013

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rdf:type	Item
description	videnskabelig artikel (da) article científic (ca) articolo scientifico (it) artigo científico (pt) bilimsel makale (tr) vedecký článok (sk) vetenskaplig artikel (sv) vědecký článek (cs) wetenschappelijk artikel (nl) wissenschaftlicher Artikel (de) научни чланак (sr) article scientifique (fr) artículu científicu espublizáu en 2013 (ast) наукова стаття, опублікована в травні 2013 (uk) scientific article published on 15 May 2013 (en) مقالة علمية نشرت في 15 مايو 2013 (ar)
publication date	wds:Q37030381-80D04E85-9CC8-4A51-A6EE-68835400DC96
publication date	2013-05-15 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q37030381-06BD7181-5373-4BBA-935E-725A6E05222E
language of work or name	English
cites work	wds:Q37030381-0C4757C3-288B-40D5-9814-EBD4B55F5361 wds:Q37030381-19223973-A0B7-424A-B475-3EBB58B17713 wds:Q37030381-26C5C603-38C3-4CE8-9FA0-5E973909DAFC wds:Q37030381-27AF3D5E-215E-4BC1-9C9C-497C6C126810 wds:Q37030381-3CC306E8-7601-4199-9450-0BC4EC77CC6E wds:Q37030381-4F5B9578-27D7-487C-9574-9E2989D4D841 wds:Q37030381-7BE4BD7A-C65B-4C9E-9AF6-9B9EA3171060 wds:Q37030381-84ABB28A-355A-4497-ADAC-9463515D32CA wds:Q37030381-AD392FD0-A8F2-4684-907F-C3AD7ED96F18 wds:Q37030381-BC3E2C67-A285-4379-ADE8-D45ECF38EC8A wds:Q37030381-BD75CB7D-8B7C-4E68-BDA6-C1D73D87BF02 wds:Q37030381-C01DE164-C0A6-4AB4-9BF7-77547DA3B7D3 wds:Q37030381-D7936A72-4463-445E-ADE9-F9AF8F36895F wds:Q37030381-DAA24386-7B77-4738-94E3-829540DC62D1 wds:Q37030381-E07EAE98-9F85-4A86-8FE0-AC72A000B09B wds:Q37030381-EB4103CF-663A-4366-AC0A-7EC346C26930
cites work	Design and Preparation of New Palladium Precatalysts for C-C and C-N Cross-Coupling Reactions Palladium-catalyzed cross-coupling of aryl chlorides and triflates with sodium cyanate: a practical synthesis of unsymmetrical ureas A bulky biaryl phosphine ligand allows for palladium-catalyzed amidation of five-membered heterocycles as electrophiles An Efficient System For the Pd-Catalyzed Cross-Coupling of Amides and Aryl Chlorides Water-mediated catalyst preactivation: an efficient protocol for C-N cross-coupling reactions The selective reaction of aryl halides with KOH: synthesis of phenols, aromatic ethers, and benzofurans A single phosphine ligand allows palladium-catalyzed intermolecular C-O bond formation with secondary and primary alcohols Formation of ArF from LPdAr(F): catalytic conversion of aryl triflates to aryl fluorides A new palladium precatalyst allows for the fast Suzuki-Miyaura coupling reactions of unstable polyfluorophenyl and 2-heteroaryl boronic acids A new biarylphosphine ligand for the Pd-catalyzed synthesis of diaryl ethers under mild conditions A new class of easily activated palladium precatalysts for facile C-N cross-coupling reactions and the low temperature oxidative addition of aryl chlorides Completely N1-selective palladium-catalyzed arylation of unsymmetric imidazoles: application to the synthesis of nilotinib Synthesis of imidazo[4,5-b]pyridines and imidazo[4,5-b]pyrazines by palladium catalyzed amidation of 2-chloro-3-amino-heterocycles Highly regioselective palladium-catalyzed direct arylation of oxazole at C-2 or C-5 with aryl bromides, chlorides, and triflates C-O cross-coupling of activated aryl and heteroaryl halides with aliphatic alcohols Catalyst-controlled chemoselective arylation of 2-aminobenzimidazoles
author name string	wds:Q37030381-9BBE44BE-5332-4907-BCB4-208057AAA66A
author name string	Nicholas C Bruno
rdfs:label	Synthesis and application of palladium precatalysts that accommodate extremely bulky di-tert-butylphosphino biaryl ligands (en) Synthesis and application of palladium precatalysts that accommodate extremely bulky di-tert-butylphosphino biaryl ligands (nl) Synthesis and application of palladium precatalysts that accommodate extremely bulky di-tert-butylphosphino biaryl ligands (ast)
skos:prefLabel	Synthesis and application of palladium precatalysts that accommodate extremely bulky di-tert-butylphosphino biaryl ligands (en) Synthesis and application of palladium precatalysts that accommodate extremely bulky di-tert-butylphosphino biaryl ligands (nl) Synthesis and application of palladium precatalysts that accommodate extremely bulky di-tert-butylphosphino biaryl ligands (ast)
name	Synthesis and application of palladium precatalysts that accommodate extremely bulky di-tert-butylphosphino biaryl ligands (en) Synthesis and application of palladium precatalysts that accommodate extremely bulky di-tert-butylphosphino biaryl ligands (nl) Synthesis and application of palladium precatalysts that accommodate extremely bulky di-tert-butylphosphino biaryl ligands (ast)
author	wds:Q37030381-45D39192-092E-44C0-9E2C-68C87913E32C
author	Stephen L. Buchwald
title	wds:Q37030381-B14E5FF5-34C7-4DEC-9038-A3E338724387
title	Synthesis and application of palladium precatalysts that accommodate extremely bulky di-tert-butylphosphino biaryl ligands (en)
page(s)	wds:Q37030381-7D31C47C-4194-4C75-9FF0-98792E7E40E5
page(s)	2876-2879
instance of	wds:Q37030381-4768BEF4-29C3-4EF3-8905-71C77AE833FF
instance of	scholarly article
main subject	wds:Q37030381-04082A3C-863F-4F8C-B726-D8EA1BAEA954
main subject	palladium
PubMed ID	wds:Q37030381-A64C29CF-8EF1-43C7-A98B-2B866867C14D
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/23675976
PubMed ID	23675976
published in	wds:Q37030381-E2B93A43-13F7-46FB-A7DC-184561F0094C
published in	Organic Letters
issue	wds:Q37030381-1CA820AB-7164-48B0-824D-2AE958B6FC4B
volume	wds:Q37030381-8DA4BF17-9299-4A29-BD79-7D6A0519C935
issue	11
volume	15
DOI	wds:Q37030381-8D2A5769-912F-4AE6-B160-5C184B5C4094
DOI	http://dx.doi.org/10.1021/OL401208T
DOI	10.1021/OL401208T
PMCID	wds:Q37030381-AFC569C8-3A2B-4112-8B66-D2838D79778D
PMCID	3717594
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q37030381
is cites work of	N-substituted 2-aminobiphenylpalladium methanesulfonate precatalysts and their use in C-C and C-N cross-couplings Mild and highly selective palladium-catalyzed monoarylation of ammonia enabled by the use of bulky biarylphosphine ligands and palladacycle precatalysts A general, practical palladium-catalyzed cyanation of (hetero)aryl chlorides and bromides. An improved catalyst system for the Pd-catalyzed fluorination of (hetero)aryl triflates Palladium-catalyzed regioselective arylation of 1,1,3-triaryl-2-azaallyl anions with aryl chlorides Synthesis of diarylmethylamines via palladium-catalyzed regioselective arylation of 1,1,3-triaryl-2-azaallyl anions NiXantphos: a deprotonatable ligand for room-temperature palladium-catalyzed cross-couplings of aryl chlorides Suzuki-Miyaura cross-coupling optimization enabled by automated feedback A General and Practical Palladium-Catalyzed Direct α-Arylation of Amides with Aryl Halides Pd-catalyzed α-arylation of trimethylsilyl enolates of α,α-difluoroacetamides Pd-catalyzed α-arylation of α,α-difluoroketones with aryl bromides and chlorides. A route to difluoromethylarenes

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