Highly functionalized organomagnesium reagents prepared through halogen-metal exchange. - Wikidata - wikimedia - TriplyDB

Highly functionalized organomagnesium reagents prepared through halogen-metal exchange.

Highly functionalized organomagnesium reagents prepared through halogen-metal exchange.

http://www.wikidata.org/entity/Q34264193

about

Nickel/bis(oxazoline)-catalyzed asymmetric Kumada reactions of alkyl electrophiles: cross-couplings of racemic alpha-bromoketones Rapid heteroatom transfer to arylmetals utilizing multifunctional reagent scaffolds.Palladium-catalyzed conversion of aryl and vinyl triflates to bromides and chlorides "Black Swan events" in organic synthesis.Engaging unactivated alkyl, alkenyl and aryl iodides in visible-light-mediated free radical reactions.Advances in transition metal (Pd, Ni, Fe)-catalyzed cross-coupling reactions using alkyl-organometallics as reaction partners An improved palladium-catalyzed conversion of aryl and vinyl triflates to bromides and chlorides.One-pot decarboxylative acylation of N-, O-, S-nucleophiles and peptides with 2,2-disubstituted malonic acids.Total synthesis of clostrubin.Practical carbon-carbon bond formation from olefins through nickel-catalyzed reductive olefin hydrocarbonation.Linchpin synthons: metalation of aryl bromides bearing a potassium trifluoroborate moiety.The Pennsylvania Green Fluorophore: a hybrid of Oregon Green and Tokyo Green for the construction of hydrophobic and pH-insensitive molecular probes.Palladium-catalyzed reactions of arylindium reagents prepared directly from aryl iodides and indium metal Metalated Nitriles: Stereodivergent Cation-Controlled Cyclizations1.Carbene-catalysed reductive coupling of nitrobenzyl bromides and activated ketones or imines via single-electron-transfer process.Stille coupling via C-N bond cleavage.Copper-catalyzed asymmetric addition of olefin-derived nucleophiles to ketones.Practical catalytic asymmetric synthesis of diaryl-, aryl heteroaryl-, and diheteroarylmethanols.Synthesis of the spiroiminal moiety and approaches to the synthesis of marineosins A and B.Simple, Efficient and Controllable Synthesis of Iodo/Di-iodoarenes via Ipsoiododecarboxylation/Consecutive Iodination Strategy.Regio- and chemoselective metalation of arenes and heteroarenes using hindered metal amide bases.Functionalization of heterocyclic compounds using polyfunctional magnesium and zinc reagents.The chemistry of the polycyclic polyprenylated acylphloroglucinols.Metal-catalyzed activation of ethers via C-O bond cleavage: a new strategy for molecular diversity.Asymmetric conjugate additions and allylic alkylations using nucleophiles generated by hydro- or carbometallation.Progress and developments in the turbo Grignard reagent i-PrMgCl·LiCl: a ten-year journey.Bromine-lithium exchange: An efficient tool in the modular construction of biaryl ligands.Palladium-catalyzed intramolecular reductive olefin hydrocarbonation: benzylic hydrogen serving as a new hydrogen donor.Shuttle Catalysis-New Strategies in Organic Synthesis.Transition-Metal-Catalyzed Electrophilic Amination: Application of O-Benzoylhydroxylamines in the Construction of the C-N Bond.Total syntheses of isonaamine C and isonaamidine E Efficient and Scalable Synthesis of 4-Carboxy-Pennsylvania Green Methyl Ester: A Hydrophobic Building Block for Fluorescent Molecular Probes Synthetic Efforts Toward [3.3.1] Bridged Bicyclic Phloroglucinol Natural Products.Perylenequinone natural products: total syntheses of the diastereomers (+)-phleichrome and (+)-calphostin D by assembly of centrochiral and axial chiral fragments.Concise and Practical Asymmetric Synthesis of a Challenging Atropisomeric HIV Integrase Inhibitor.Bromination of hydrocarbons with CBr4, initiated by light-emitting diode irradiation.Total Syntheses of Naamidine G and 14-Methoxynaamidine G.Ring opening of pymisyl-protected aziridines with organocuprates.Transition-metal-free synthesis of conjugated polymers from bis-Grignard reagents by using TEMPO as oxidant.A convenient synthesis of benzonitriles via electrophilic cyanation with N-cyanobenzimidazole.

P2860

Q33623320-91B27640-0611-400E-A3D3-F0D7ED7C7403 Q33833213-632576D3-0E74-4917-91C7-BFC177CE5140 Q34287143-46ABCD86-A8F2-4421-8272-5C8EC4101E06 Q34294027-C4771B27-2657-4AB4-B705-D80C0BCA2DC3 Q34301296-FCA2A99C-6376-42AD-82F0-C9941EB687D9 Q34788016-8D96C386-2E48-4E90-AACE-B1B7D2052163 Q35206680-84BF8FA3-0ED8-4601-AB1B-47BB756CAD0A Q35213765-719E1712-5FCB-4ABD-807A-361A2A42A1DA Q35245011-935D2D3B-6E68-41F9-B203-32E836E4C3FD Q36768656-B1C3CC19-FF3C-4882-8F85-20C275F00564 Q36823431-39338DBF-A326-4794-B0D4-C6305ACB4417 Q36865543-8734615C-BB26-4CAB-B4D2-FE0C946557F3 Q36901531-F5774266-2397-4152-A99E-B3E16FEB73C6 Q37004257-8BCE9AF8-87B8-4DB4-A735-5EB2635B147D Q37315016-E03F253B-687A-46A2-8A96-2FEC9F5AF991 Q37324108-72AABC6A-5814-4D88-8F3E-4F008AE644C4 Q37336485-5A35A70F-6093-457D-AA9F-3FB63FD482C4 Q37370256-D5FFBAA4-1784-4ECA-BD15-D72A088AD5D0 Q37454375-5FCEC1A8-ED27-484F-BF95-872C5C8B4F51 Q37587710-A4FC31F4-1FD2-4FBC-BEC0-1A0FC21918D0 Q37939746-FD042DAF-04DD-4EBE-98D9-DA22D8A6EDC7 Q37942897-FFA4073E-ACCA-42F5-86E4-772613D2AC7A Q37998425-DC513729-1362-4C2D-9DA2-78694162C11A Q38243353-4FA80EE8-09BF-4B55-8BE9-AB6D65B5294D Q38325282-F4E9D24E-4E40-45AC-BE94-61B4C2C4E1DF Q38562356-355D886F-2FDE-4B34-A066-88E8F67718EC Q38586638-70553A8E-7306-4A33-A7BF-A90DA09BC259 Q38733720-808C3F81-DDAB-42A9-B43C-BC08B45CFFA8 Q38765611-D48A16A0-848A-45D5-9A83-615FD3CEDDC9 Q38908370-9986EEFD-7CCB-4047-994C-C49841D9DC26 Q39435522-5741C3F2-26C6-424F-9B47-8AA8FF47E849 Q40392035-B42427CD-8C44-4BCF-9896-7D33CB41C16F Q41480932-8EFAEA4E-DE65-4DF4-83E7-D6351970BBFB Q41940361-BE2DB3FF-A682-4C0A-8262-CC3DA1F39357 Q42144330-D81AB2E9-41A0-473E-BF1B-355C2397ABA8 Q42154339-08DD8E02-E4D8-43B4-AD21-1BA02AF89690 Q42215985-24B7F4C3-0F90-4B56-88EB-7527BB3A4988 Q42908184-0BEF5275-4866-4519-A7CF-5C23CD727E67 Q43089296-9FA45524-EEEE-469D-B61D-79350AF9488C Q43121345-D0955BE0-AF0B-4758-AE2D-89415D7D69DF

P2860

Highly functionalized organomagnesium reagents prepared through halogen-metal exchange.

http://www.wikidata.org/entity/Q34264193

description

2003 nî lūn-bûn

@nan

2003 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2003 թվականի սեպտեմբերին հրատարակված գիտական հոդված

@hy

2003年の論文

@ja

2003年論文

@yue

2003年論文

@zh-hant

2003年論文

@zh-hk

2003年論文

@zh-mo

2003年論文

@zh-tw

2003年论文

@wuu

name

Highly functionalized organomagnesium reagents prepared through halogen-metal exchange.

@ast

Highly functionalized organomagnesium reagents prepared through halogen-metal exchange.

@en

Highly functionalized organomagnesium reagents prepared through halogen-metal exchange.

@nl

type

label

Highly functionalized organomagnesium reagents prepared through halogen-metal exchange.

@ast

Highly functionalized organomagnesium reagents prepared through halogen-metal exchange.

@en

Highly functionalized organomagnesium reagents prepared through halogen-metal exchange.

@nl

prefLabel

Highly functionalized organomagnesium reagents prepared through halogen-metal exchange.

@ast

Highly functionalized organomagnesium reagents prepared through halogen-metal exchange.

@en

Highly functionalized organomagnesium reagents prepared through halogen-metal exchange.

@nl

P1433

Q34264193-972DD0ED-6B73-4AB7-A8E5-518005BC9EAB

P1476

Q34264193-C519512B-C9BD-46AB-8A77-FFF2087C04D0

P2093

Q34264193-1DCCF0A7-A664-497F-9D0D-2670F725FB5D

Q34264193-43B813DA-CDBC-4C78-A7AC-CEE967441536

Q34264193-522A4D4B-7288-4E7F-831D-EA87D839E120

Q34264193-7BCCA24A-8A7C-4F4C-8130-C9B567D9E1B3

Q34264193-7FF5E589-99ED-4211-BB15-45F9AC11428F

Q34264193-A38E0A9A-863B-49FD-B673-80FBDD6B93BB

Q34264193-EB3B83E7-091C-4222-B877-9FE76703F838

P2860

Q34264193-03522A71-02D3-4B9F-ABA6-315D8E5C2DF3

Q34264193-0C3134E7-B171-4909-9F93-BDDF32DD7877

Q34264193-17B27610-A225-4467-9F40-66A90E30BE33

Q34264193-1D5D8C71-F0C2-4F7B-9D3A-B7CE0C516475

Q34264193-2CFD41E7-76B5-4C7F-9D57-7790AB4620CC

Q34264193-31DBC39B-87DC-4C2A-A35D-71B123A95981

Q34264193-3D553404-196B-4507-A6FC-BA5E110D1E60

Q34264193-47BC0552-DC5F-474A-BF1D-6EA6886EEFE6

Q34264193-4C3A2FEB-9A1C-4D72-90DC-CFFF03BA0A30

Q34264193-510EEFB0-0BAD-4058-A6C5-562408B6F229

P304

Q34264193-ED5206EC-977B-45F9-AA68-010619F7B4D1

P31

Q34264193-D9A0B6CD-D734-4541-8BBE-2F1AE45DA81F

P356

Q34264193-32FC8B1E-E38C-4003-978B-21BA7278109D

P407

Q34264193-E88296C5-B7EA-446C-B15E-12830F30C9F8

P433

Q34264193-84368350-1A2C-4552-AB01-1D140E624F76

P478

Q34264193-E6581C7E-A361-4D92-B991-2D1A5211615E

P50

Q34264193-F2270102-FC23-43ED-8947-EB522CD7396B

P577

Q34264193-912D381F-7939-48D7-A976-E208CC02ED49

P698

Q34264193-BC245C60-D3D8-4762-8EBF-418F8FB9093B

P356

P1433

Angewandte Chemie International Edition

P1476

Highly functionalized organomagnesium reagents prepared through halogen-metal exchange.

@en

P2093

Felix Kopp

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

Florian F Kneisel

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

Ioannis Sapountzis

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

Nina Gommermann

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

Tobias Korn

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

Viet Anh Vu

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

Wolfgang Dohle

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

P2860

Low-temperature formation of functionalized Grignard reagents from direct oxidative addition of active magnesium to aryl bromides

Preparation of organometallic compounds from highly reactive metal powders

Vinylation of Grignard reagents. Catalysis by iron

Rational Development of Practical Catalysts for Aromatic Carbon−Nitrogen Bond Formation

Synthesis of a muscarinic receptor antagonist via a diastereoselective Michael reaction, selective deoxyfluorination and aromatic metal-halogen exchange reaction.

Total synthesis of (+)-phorboxazole A exploiting the Petasis-Ferrier rearrangement.

Alkynyliodonium salts in organic synthesis. Application to the total synthesis of the tropoloisoquinoline alkaloid pareitropone.

Application of Baldwin's rules for the preparation of stable, beta-leaving group-bearing organolithium compounds.

The first general method for palladium-catalyzed Negishi cross-coupling of aryl and vinyl chlorides: use of commercially available Pd(P(t-Bu)(3))(2) as a catalyst.

Total Synthesis of Vancomycin Aglycon-Part 3: Final Stages.

P304

4302-4320

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

P31

scholarly article

P356

10.1002/ANIE.200300579

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

P407

P433

36

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

P478

42

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

P50

P577

2003-09-01T00:00:00Z

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

P698

14502700

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