Nitrosation of aryl and heteroaryltrifluoroborates with nitrosonium tetrafluoroborate - Wikidata - awgldk - TriplyDB

Nitrosation of aryl and heteroaryltrifluoroborates with nitrosonium tetrafluoroborate

Nitrosation of aryl and heteroaryltrifluoroborates with nitrosonium tetrafluoroborate

http://www.wikidata.org/entity/Q42149283

about

Stereo- and regioselectivity of the hetero-Diels-Alder reaction of nitroso derivatives with conjugated dienes Copper-mediated N-Arylation of Methyl 2-Aminothiophene-3-carboxylate with Organoboron Reagents Recent advances in the synthesis of aromatic nitro compounds.Selection of boron reagents for Suzuki-Miyaura coupling.Transition-Metal-Free ipso-Functionalization of Arylboronic Acids and Derivatives.Elusive metal-free primary amination of arylboronic acids: synthetic studies and mechanism by density functional theory.Synthesis of trifluoromethylated isoxazolidines: 1,3-dipolar cycloaddition of nitrosoarenes, (trifluoromethyl)diazomethane, and alkenes.A Lewis Acid Catalyzed annulation to 2,1-benzisoxazoles Arylation and heteroarylation of thienylsulfonamides with organotrifluoroborates.A Promising PET Tracer for Imaging of α₇ Nicotinic Acetylcholine Receptors in the Brain: Design, Synthesis, and in Vivo Evaluation of a Dibenzothiophene-Based Radioligand.Copper-Catalyzed Mild Nitration of Protected Anilines

P2860

Q28075988-15860614-A957-41D2-A364-CA7AFA42EECE Q36275584-8B8C0AF3-7C37-4C3D-8E17-8CC726177D7B Q38084910-3AC9CC43-3EE2-4A7F-8841-5FD7F568744F Q38148935-1306E37D-2902-4516-92E0-A66A313DD4B3 Q38270169-6ED3DA7E-C3B6-4886-ACA3-C3517D455B5C Q41259436-DE8FAA7E-2506-4868-8041-5153736E83DC Q41914414-7C793F4C-E557-4038-8E37-446B0FA5C4F8 Q41969722-1BC4C556-814F-401D-9736-40A79C47090B Q42090837-16058F3B-9FDB-4602-B693-BAC05CCD99BB Q52147865-4F738A12-5B01-4057-B93A-876D05E6305F Q58139970-B4C49010-5DED-46D3-AFBA-5A0CA33FE33A

P2860

Nitrosation of aryl and heteroaryltrifluoroborates with nitrosonium tetrafluoroborate

http://www.wikidata.org/entity/Q42149283

description

2012 nî lūn-bûn

@nan

2012年の論文

@ja

2012年論文

@yue

2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

@zh-tw

2012年论文

@wuu

2012年论文

@zh

2012年论文

@zh-cn

name

Nitrosation of aryl and heteroaryltrifluoroborates with nitrosonium tetrafluoroborate

@en

Nitrosation of aryl and heteroaryltrifluoroborates with nitrosonium tetrafluoroborate

@nl

type

label

Nitrosation of aryl and heteroaryltrifluoroborates with nitrosonium tetrafluoroborate

@en

Nitrosation of aryl and heteroaryltrifluoroborates with nitrosonium tetrafluoroborate

@nl

prefLabel

Nitrosation of aryl and heteroaryltrifluoroborates with nitrosonium tetrafluoroborate

@en

Nitrosation of aryl and heteroaryltrifluoroborates with nitrosonium tetrafluoroborate

@nl

P1433

Q42149283-42B1CB93-4693-4E6B-BD63-34F5C796FC0B

P1476

Q42149283-2223761D-ABCA-443A-A968-435D000E59D6

P2093

Q42149283-2C9149D2-85EA-4C4B-AF0A-F4D996AB0A68

P2860

Q42149283-026B5768-E473-4CBE-B121-D09107BFA5CD

Q42149283-05B22411-7C12-4E55-8E4D-54CD1E151946

Q42149283-1181AA99-D101-48AC-99AF-B476D66F314B

Q42149283-2ACBF6A7-D7D6-4CA9-8B26-952CCC020657

Q42149283-2E4B9BC1-933F-4932-BDCB-957E4DA78732

Q42149283-367EF359-B123-435A-9F30-B99D8A011308

Q42149283-3A096C19-403F-414C-9339-2BDE8C804A8C

Q42149283-43F46E45-B3F8-47C0-9F7D-901BD87FAA17

Q42149283-49E77486-4B0C-4102-9F95-A12EC3A733B1

Q42149283-51035BF6-99C5-4A32-8366-24CEDD8303DC

P304

Q42149283-8722F3B3-EA30-4FCF-AC85-8A4AF39A66E2

P31

Q42149283-3F10A579-69C2-4CF5-98F0-480E80142325

P356

Q42149283-5F84C5CE-C251-4152-97EA-2129A8062A4A

P407

Q42149283-40C89626-7EA9-4492-AB79-AD2F9C3CD86E

P433

Q42149283-1EA523C2-1958-4E90-99E3-8CC9800D6EBA

P478

Q42149283-80CF96B3-F4F6-4F04-A07C-33C846CFAD51

P50

Q42149283-148706AC-D14F-438D-A7C3-E31CA4954468

P577

Q42149283-810D5BEF-3BDE-41EF-B816-9EF4D96B3B82

P698

Q42149283-0BB87060-69DD-43D6-81E7-7525CCB1B0D2

P932

Q42149283-B0049ADE-A67E-4542-9889-DB8169506F8A

P356

P1433

Journal of Organic Chemistry

P1476

Nitrosation of aryl and heteroaryltrifluoroborates with nitrosonium tetrafluoroborate

@en

P2093

Livia N Cavalcanti

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

P2860

Bronsted acid catalysis of achiral enamine for regio- and enantioselective nitroso aldol synthesis

Oxidation of organotrifluoroborates via oxone

A Review of the Selective Catalytic Reduction of Aromatic Nitro Compounds into Aromatic Amines, Isocyanates, Carbamates, and Ureas Using CO.

Photochemical reaction mechanisms of 2-nitrobenzyl compounds: methyl ethers and caged ATP.

Optical switching and image storage by means of azobenzene liquid-crystal films.

Catalytic, highly enantio, and diastereoselective nitroso diels-alder reaction.

Catalytic asymmetric nitroso-Diels-Alder reaction with acyclic dienes.

Organotrifluoroborates: protected boronic acids that expand the versatility of the Suzuki coupling reaction.

Potassium organotrifluoroborates: new perspectives in organic synthesis.

Preparations of C-nitroso compounds.

P304

4402-4413

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

P31

scholarly article

P356

10.1021/JO300551M

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

P407

P433

9

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

P478

77

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

P50

Gary A Molander

P577

2012-04-24T00:00:00Z

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

P698

22524190

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

P932

3345084

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