Boronic acids: new coupling partners in room-temperature Suzuki reactions of alkyl bromides. Crystallographic characterization of an oxidative-addition adduct generated under remarkably mild conditions.

Boronic acids: new coupling partners in room-temperature Suzuki reactions of alkyl bromides. Crystallographic characterization of an oxidative-addition adduct generated under remarkably mild conditions.

Item

http://www.wikidata.org/entity/Q34158924

Q34158924

about

Rational exploration of N-heterocyclic carbene (NHC) palladacycle diversity: a highly active and versatile precatalyst for Suzuki-Miyaura coupling reactions of deactivated aryl and alkyl substrates.Organotrifluoroborates and monocoordinated palladium complexes as catalysts--a perfect combination for Suzuki-Miyaura coupling.Total synthesis of a noricumazole A library and evaluation of HCV inhibition.PALLADIUM-CATALYZED ALKYL-ALKYL SUZUKI CROSS-COUPLINGS OF PRIMARY ALKYL BROMIDES AT ROOM-TEMPERATURE: (13-CHLOROTRIDECYLOXY)TRIETHYLSILANE [Silane, [(13-chlorotridecyl)oxy]triethyl-].Advances in transition metal (Pd, Ni, Fe)-catalyzed cross-coupling reactions using alkyl-organometallics as reaction partners Suzuki coupling of potassium cyclopropyl- and alkoxymethyltrifluoroborates with benzyl chlorides.Palladium-catalyzed hydrofunctionalization of vinyl phenol derivatives with heteroaromatics Click with a boronic acid handle: a neighboring group-assisted click reaction that allows ready secondary functionalization.A mild, palladium-catalyzed method for the dehydrohalogenation of alkyl bromides: synthetic and mechanistic studies Selective synthesis of 5- or 6-aryl octahydrocyclopenta[b]pyrroles from a common precursor through control of competing pathways in a Pd-catalyzed reaction.Ligand-accelerated ortho-C-H alkylation of arylcarboxylic acids using alkyl boron reagents.Palladium-catalyzed hydroalkylation of styrenes with organozinc reagents to form carbon-carbon sp3-sp3 bonds under oxidative conditions.Pd-catalyzed cross-coupling reactions of alkyl halides.Stereospecific Ni-catalyzed cross-coupling of potassium alkenyltrifluoroborates with alkyl halides.Ligand-Promoted Borylation of C(sp(3))-H Bonds with Palladium(II) Catalysts.Suzuki-Miyaura cross-coupling reactions of primary alkyltrifluoroborates with aryl chlorides.Nickel-catalyzed cross-coupling of potassium aryl- and heteroaryltrifluoroborates with unactivated alkyl halides.Palladium-catalyzed ligand-promoted site-selective cyanomethylation of unactivated C(sp3)-H bonds with acetonitrile.Dichloro-bis(aminophosphine) complexes of palladium: highly convenient, reliable and extremely active suzuki-miyaura catalysts with excellent functional group tolerance.Oxidative addition to palladium(0) diphosphine complexes: observations of mechanistic complexity with iodobenzene as reactant.Facile synthesis of trifluoroethyl compounds by the Suzuki cross-coupling reactions of CF3CH2OTs with arylboronic acids.Spectroscopic characterization of (diiodomethyl)zinc iodide: application to the stereoselective synthesis and functionalization of iodocyclopropanes.Highly nucleophilic vitamin B12-assisted nickel-catalysed reductive coupling of aryl halides and non-activated alkyl tosylates.A Dual Palladium and Copper Hydride Catalyzed Approach for Alkyl-Aryl Cross-Coupling of Aryl Halides and Olefins.Evolution of an Efficient and Scalable Nine-Step (Longest Linear Sequence) Synthesis of Zincophorin Methyl Ester.A Pd-catalyzed, boron ester-mediated, reductive cross-coupling of two aryl halides to synthesize tricyclic biaryls.An Improved System for the Aqueous Lipshutz-Negishi Cross-Coupling of Alkyl Halides with Aryl Electrophiles.Synthesis of E- and Z-trisubstituted alkenes by catalytic cross-metathesis.Palladium-catalyzed intramolecular reductive cross-coupling of Csp2-Csp3 bond formation.Transfer of aryl halide to alkyl halide: reductive elimination of alkylhalide from alkylpalladium halides containing syn-β-hydrogen atoms.Modular Stereoselective Synthesis of (1→2)-C-Glycosides based on the sp(2) -sp(3) Suzuki-Miyaura Reaction.Copper‐Catalyzed Borylation of Cyclic Sulfamidates: Access to Enantiomerically Pure (β‐and γ‐Aminoalkyl)boronic Esters.Copper-Catalyzed Cross-Coupling Reaction of Organoboron Compounds with Primary Alkyl Halides and Pseudohalides General Strategies for the Synthesis of Liquid Crystals

P2860

Q33533417-86A755E7-2A80-4545-AE64-313B0DBDEF69 Q34051116-80A6489A-8A51-4641-BA54-BD906685C06E Q34303738-85C5F645-00F7-4F0E-9B52-C1EE6C33F8BC Q34433651-E2741F3F-60F4-4FE7-81D5-548DF5C6819E Q34788016-4571143C-1C8C-43AD-BC6D-3BD232BCE6AC Q35836362-E1BC07A9-E945-4A2C-88EC-0EBD84F3D076 Q35882654-A792400D-9AF4-43E0-AFBE-5A0117CA74FB Q36154919-AF49E88E-814E-440E-B3B4-3D2F894F47B0 Q36206042-6CEF45D5-CFD3-481D-B35F-5CC17DE9EEF8 Q37328935-208010A9-F8A8-4A60-B566-074CBB2A91EE Q37427713-B9A03268-B629-4BA0-AF31-4A2802497FA0 Q37480212-DB6BCB81-F6AE-4A4C-A2E8-B9CB6385470E Q37904753-A58652FB-EFE1-4043-AC25-4A2D3D205CCE Q38859731-F75CAF5C-7AF0-4BBD-9B7F-10CA5F353C4F Q39877406-D234A168-C2CE-42E6-AF3A-E011099F3A6A Q41479807-673B2CA3-5C20-403F-9ADF-4706C0748B5E Q41840604-DA91D3AE-E275-4258-9F08-108E8E601ED0 Q41903560-D5F70113-9D0E-40D5-BF7A-F7BA42494616 Q43148463-964254E2-ADA5-4884-93CD-45C2DE0D00E9 Q43497416-FE020673-F7E4-4FE3-B269-8660F3BDC493 Q44694239-52AFD9B5-2E42-44B5-8181-6ED2FD59F683 Q46320831-587B3612-3835-4AFD-BFC3-E474C620CEB8 Q46376028-769C452A-9E91-4D1C-89B4-7A8B2907DA83 Q48136710-F213D1AE-4A9C-47E5-BBC4-1E59CAF49A7B Q48155588-17DBF833-AC79-4046-B62C-0750AAFF8A71 Q48203605-2B24C82E-2A8D-429B-BA1B-C41C2CD41CE3 Q48279482-AC796158-7351-4E8E-A539-E90401FDE6F6 Q48553060-0F491306-5720-40AA-9AD8-AD1C8F352776 Q50455391-57472FDA-1237-4FA3-8E13-3D47CD0C9146 Q53398512-F9B83B56-0550-49BC-B855-7203A95401A2 Q53757285-327D8EB1-77E4-4307-8958-7D0978A074DD Q54962288-0D8B89FE-D8F7-4AD2-AD6E-899F71000240 Q56482603-8239E00D-C26A-484D-BD4E-9665153EBD3E Q57817022-38CDC43A-7905-4C85-87CC-A0C6D9195F20

P2860

Boronic acids: new coupling partners in room-temperature Suzuki reactions of alkyl bromides. Crystallographic characterization of an oxidative-addition adduct generated under remarkably mild conditions.

Item

http://www.wikidata.org/entity/Q34158924

description

2002 nî lūn-bûn

@nan

2002 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2002 թվականի նոյեմբերին հրատարակված գիտական հոդված

@hy

2002年の論文

@ja

2002年論文

@yue

2002年論文

@zh-hant

2002年論文

@zh-hk

2002年論文

@zh-mo

2002年論文

@zh-tw

2002年论文

@wuu