Synthesis of catechols from phenols via Pd-catalyzed silanol-directed C-H oxygenation. - Wikidata - wikimedia - TriplyDB

Synthesis of catechols from phenols via Pd-catalyzed silanol-directed C-H oxygenation.

Synthesis of catechols from phenols via Pd-catalyzed silanol-directed C-H oxygenation.

http://www.wikidata.org/entity/Q35648469

about

The Toluene o-Xylene Monooxygenase Enzymatic Activity for the Biosynthesis of Aromatic Antioxidants Double-fold C-H oxygenation of arenes using PyrDipSi: a general and efficient traceless/modifiable silicon-tethered directing group.General method for the synthesis of salicylic acids from phenols through palladium-catalyzed silanol-directed C-H carboxylation Pd-catalyzed modifiable silanol-directed aromatic C-H oxygenation Pd(II)-catalyzed enantioselective C-H activation/C-O bond formation: synthesis of chiral benzofuranones.Pd(II)-catalyzed ortho- or meta-C-H olefination of phenol derivatives Catalytic phenol hydroxylation with dioxygen: extension of the tyrosinase mechanism beyond the protein matrix.General and practical carboxyl-group-directed remote C-H oxygenation reactions of arenes.Catalytic Reductive ortho-C-H Silylation of Phenols with Traceless, Versatile Acetal Directing Groups and Synthetic Applications of Dioxasilines A redox-neutral catechol synthesis.Arene C-H functionalisation using a removable/modifiable or a traceless directing group strategy.A new phenolic derivative with soluble epoxide hydrolase and nuclear factor-kappaB inhibitory activity from the aqueous extract of Acacia catechu.Accessing Drug Metabolites via Transition-Metal Catalyzed C-H Oxidation: The Liver as Synthetic Inspiration.Twofold unsymmetrical C-H functionalization of PyrDipSi-substituted arenes: a general method for the synthesis of substituted meta-halophenols.Meta-selective C-H functionalization using a nitrile-based directing group and cleavable Si-tether.A Highly Selective Vanadium Catalyst for Benzylic C-H Oxidation.Stereoselective synthesis of silicon-stereogenic aminomethoxysilanes: easy access to highly enantiomerically enriched siloxanes.Palladium-catalyzed ortho-alkenylation of aryl hydrogen phosphates using a new mono-phosphoric acid directing group.Ketimido metallophthalocyanines: an approach to phthalocyanine-supported mononuclear high-valent ruthenium complexes.Broadening the catalyst and reaction scope of regio- and chemoselective C-H oxygenation: a convenient and scalable approach to 2-acylphenols by intriguing Rh(II) and Ru(II) catalysis.Metal-free oxidation of aromatic carbon-hydrogen bonds through a reverse-rebound mechanism.Synthesis of ortho-Azophenols by Formal Dehydrogenative Coupling of Phenols and Hydrazines or Hydrazides.Silicon-Tethered Strategies for C-H Functionalization Reactions.Heterologous pathway assembly reveals molecular steps of fungal terreic acid biosynthesis.A meta-selective-C-H alkenylation of phenol-derivatives employing a traceless organosilicon template.A bentonite-gold nanohybrid as a heterogeneous green catalyst for selective oxidation of silanes.Palladium-Catalyzed Directed para C-H Functionalization of Phenols.Reductive arene ortho-silanolization of aromatic esters with hydridosilyl acetals.Dual C-H functionalization of N-aryl tetrahydroisoquinolines: a highly diastereoselective synthesis of dibenzo[a,f]quinolizines via visible-light induced oxidation and inverse electron-demand aza-Diels-Alder reaction.The design of a readily attachable and cleavable molecular scaffold for ortho-selective C–H alkenylation of arene alcohols† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c5sc03948g.A bio-inspired synthesis of oxindoles by catalytic aerobic dual C-H functionalization of phenols.Palladium-catalyzed ortho-acyloxylation of N-nitrosoanilines via direct sp2 C–H bond activation A comprehensive overview of directing groups applied in metal-catalysed C-H functionalisation chemistry Diastereotopic Group Selection in Hydroxy-Directed Intramolecular CH Alkenylation of Indole under Oxidative Palladium(II) Catalysis A New Direction in CH Alkenylation: Silanol as a Helping Hand

P2860

Q28546741-16804EA9-08B3-4DF5-9B75-158418CA8815 Q36021897-48BA9C5F-2D03-4171-A108-1C73AAA54836 Q36047548-3ABD6DA0-5A41-4DF3-8262-617CDFDF5409 Q36452868-E833A872-2CF1-4AE4-B877-838C90E5C292 Q36628264-EC5232D8-6C5D-4014-84E1-BE7F193E8076 Q36936524-893916FA-E9ED-4DFC-A0F5-77AEF05EC07E Q37271053-1079A828-6277-4C9F-9D47-77D000FF9CFE Q37374955-4B8006C0-F8BB-4E28-A1AB-68A1C2C2F70E Q37406215-DB9BA218-5981-4317-A754-0BC685C6A89E Q37622412-460C9D90-121B-41D6-927E-3F29E8293DE8 Q38225214-C7CB9E9C-BB73-455E-9E2B-93963A5CA2D7 Q38813525-14EFDEA9-C342-4775-8A88-393C13BA1981 Q38977018-746FAC98-6271-4A0E-8599-C61F0DA0F4C3 Q41819937-FA59653C-062C-4D66-ADB9-4DB6E82B98D0 Q41966616-920F8B73-33BA-47B3-B1DB-4D4ED1693301 Q42202343-CCE85D45-F5CB-4CF8-8FEB-69968A7CB065 Q43559534-35116B52-0952-4CE8-9588-E9DDE4CFE833 Q43796728-D99C8B74-A505-498A-90A0-8CE2D08936AD Q45968419-DD65B619-A72B-463C-9A8F-9D536B5351A3 Q46026417-70A6791D-A202-4BC2-8359-BEA1BFCD2F0B Q46032822-7137CCC9-531E-40C8-9EDB-01E930A34CE1 Q48089125-B6A518C7-32C0-4A85-ACC9-A96D063BA152 Q48299900-9622B446-6053-459F-9AEE-D1B0F4EE0664 Q49389431-F72D5FA0-00C6-41AB-85F1-45B8ACB604AE Q49941026-F55BC99E-F278-4EE3-AC8D-851082B57A9D Q50222165-BE8FA346-A680-4331-8E03-2749BD9409C5 Q50854910-97D5117E-FC69-45F7-B6AC-E902D881D0F9 Q51012024-FCC7FA67-C480-48CC-9946-309D627CF48D Q51631212-21A9E6BC-CB21-4999-BA56-606C87BE1377 Q55077095-388042F5-787A-459D-BC90-6510A07555B0 Q55154908-A518D76B-4988-48F9-B60F-7836350427A2 Q57614533-331A3968-4A77-4E65-BC5E-E0C54044E220 Q58420199-3479071D-BB23-43D1-8497-CE4203A9CD8F Q59203353-6CC4AD51-C8CB-4DEE-B70F-D0FAB0F79578 Q59203437-752AF35D-089E-444F-A7D0-2E0FDF52B1F8

P2860

Synthesis of catechols from phenols via Pd-catalyzed silanol-directed C-H oxygenation.

http://www.wikidata.org/entity/Q35648469

description

2011 nî lūn-bûn

@nan

2011年の論文

@ja

2011年論文

@yue

2011年論文

@zh-hant

2011年論文

@zh-hk

2011年論文

@zh-mo

2011年論文

@zh-tw

2011年论文

@wuu

2011年论文

@zh

2011年论文

@zh-cn

name

Synthesis of catechols from phenols via Pd-catalyzed silanol-directed C-H oxygenation.

@ast

Synthesis of catechols from phenols via Pd-catalyzed silanol-directed C-H oxygenation.

@en

type

label

Synthesis of catechols from phenols via Pd-catalyzed silanol-directed C-H oxygenation.

@ast

Synthesis of catechols from phenols via Pd-catalyzed silanol-directed C-H oxygenation.

@en

prefLabel

Synthesis of catechols from phenols via Pd-catalyzed silanol-directed C-H oxygenation.

@ast

Synthesis of catechols from phenols via Pd-catalyzed silanol-directed C-H oxygenation.

@en

P1433

Q35648469-9101A3FB-C8CD-4756-96E7-93E1017510A8

P1476

Q35648469-D813D62A-8F4A-4D0C-BA97-1C595C912566

P2093

Q35648469-01D8674A-81CF-4E5A-9A86-413E96BE10FE

Q35648469-21652033-0042-453F-9D68-4A1EA020D6A0

Q35648469-65DD20BB-FDA4-4079-8DAE-476B7498DAE9

Q35648469-7AEAA0F1-E8A5-429A-9C76-2F390E23979F

P2860

Q35648469-0A980657-B28F-4694-8BEA-25EE4D0A50B3

Q35648469-1B4FAC29-2484-4CD6-9A25-CFC5778045D1

Q35648469-1EDBB34B-AD20-4DF3-B354-3969C9386285

Q35648469-1FB72ACA-63B8-4F8E-8B53-DAF4F104C863

Q35648469-2FFD7E53-310E-49F1-8DA6-54E84A75BFE7

Q35648469-34A9BBC9-5F02-476A-98CE-4BF1484E4E3F

Q35648469-38C84C4B-1856-4F3D-9A84-E3A5FC119A15

Q35648469-3D183CF3-4693-4F83-AAB4-4D6BD447E29C

Q35648469-423ED9C7-90CB-4943-AD44-949074111F19

Q35648469-4A3C13C2-D1E8-484B-8DF6-FFE5EC04FE81

P304

Q35648469-C700ACE1-AF1E-4EE6-826B-B3FF650AAC72

P31

Q35648469-E61D730A-1BCA-4651-B2AF-A27771B35D7B

P356

Q35648469-18A41D61-96B9-48EC-89CA-60D72E80CD35

P407

Q35648469-B40D7CD7-DBB8-4BA6-A70A-E99BE86A748B

P433

Q35648469-4889EB35-D78C-4B6D-B25D-8EC75805D79C

P478

Q35648469-F594D18C-57B1-4BE1-BB03-7727AE6E920E

P577

Q35648469-50BB3D4A-AED3-4C70-9021-809E9DE0E912

P5875

Q35648469-E85A0C6E-8605-42FF-964D-2EEE5C869DA0

P698

Q35648469-7D8799E5-A0E7-4A03-836F-A71B0C4783FA

P932

Q35648469-54F4A672-B50F-4A6C-90EB-6DA4A3BC541C

P356

P1433

Journal of the American Chemical Society

P1476

Synthesis of catechols from phenols via Pd-catalyzed silanol-directed C-H oxygenation.

@en

P2093

Buddhadeb Chattopadhyay

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

Chunhui Huang

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

Nugzar Ghavtadze

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

Vladimir Gevorgyan

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

P2860

Regioselective oxidation of phenols to o-quinones with o-iodoxybenzoic acid (IBX)

Palladium-Catalyzed Ligand-Directed C−H Functionalization Reactions

A process optimization for bio-catalytic production of substituted catechols (3-nitrocatechol and 3-methylcatechol.

PyDipSi: a general and easily modifiable/traceless Si-tethered directing group for C-H acyloxylation of arenes.

Transition-metal-catalyzed direct arylation of (hetero)arenes by C-H bond cleavage.

Silanol: a traceless directing group for Pd-catalyzed o-alkenylation of phenols.

Aryl-aryl bond formation by transition-metal-catalyzed direct arylation.

Sigma-chelation-directed C-H functionalizations using Pd(II) and Cu(II) catalysts: regioselectivity, stereoselectivity and catalytic turnover.

Dioxygenase- and monooxygenase-catalysed synthesis of cis-dihydrodiols, catechols, epoxides and other oxygenated products.

Recent advances in aryl-aryl bond formation by direct arylation.

P304

17630-17633

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

P31

scholarly article

P356

10.1021/JA208572V

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

P407

P433

44

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

P478

133

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

P577

2011-10-18T00:00:00Z

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

P5875

51722313

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

P698

21999512

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

P932

3250381

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