About: Catalytic Allylic Oxidation of Alkenes Using an Asymmetric Kharasch-Sosnovsky Reaction

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scientific article published on 01 October 2001

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в жовтні 2001 (uk) im Oktober 2001 veröffentlichter wissenschaftlicher Artikel (de) article scientifique publié en octobre 2001 (fr) artículu científicu espublizáu n'ochobre de 2001 (ast) scientific article published on 01 October 2001 (en)
publication date	wds:Q74602532-9BDE6F80-83D9-49F4-9EF4-08E15D5CD171
publication date	2001-10-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q74602532-926E9B25-B3B4-479F-A187-8A10824EA08A wds:Q74602532-FC529A4C-97B8-406A-8555-B35EBC76631D
author name string	Michael Watkinson Jason Eames
rdfs:label	Catalytic Allylic Oxidation of Alkenes Using an Asymmetric Kharasch-Sosnovsky Reaction (en) Catalytic Allylic Oxidation of Alkenes Using an Asymmetric Kharasch-Sosnovsky Reaction (nl)
skos:prefLabel	Catalytic Allylic Oxidation of Alkenes Using an Asymmetric Kharasch-Sosnovsky Reaction (en) Catalytic Allylic Oxidation of Alkenes Using an Asymmetric Kharasch-Sosnovsky Reaction (nl)
name	Catalytic Allylic Oxidation of Alkenes Using an Asymmetric Kharasch-Sosnovsky Reaction (en) Catalytic Allylic Oxidation of Alkenes Using an Asymmetric Kharasch-Sosnovsky Reaction (nl)
title	wds:Q74602532-2F9879F5-45A6-4996-9216-D425729047D6
title	Catalytic Allylic Oxidation of Alkenes Using an Asymmetric Kharasch-Sosnovsky Reaction (en)
page(s)	wds:Q74602532-066BA896-8665-4974-A606-A87ADCBB74A0
page(s)	3567-3571
instance of	wds:Q74602532-4B510B5D-F893-4787-BD38-D85F89EAC2D3
instance of	scholarly article
PubMed ID	wds:Q74602532-E4CF25EE-ADFA-42C3-A6AD-5756FEF21E5C
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11592185
PubMed ID	11592185
published in	wds:Q74602532-BECB2637-1301-401F-BDC9-9E560D538429
published in	Angewandte Chemie International Edition
issue	wds:Q74602532-66EB6094-2B29-4C0A-BA9B-BD263E1173F3
volume	wds:Q74602532-24968013-1D34-409C-B226-869A8B736F99
issue	19
volume	40
DOI	wds:Q74602532-9D391CAC-837F-4E34-B529-342ADF134990
DOI	http://dx.doi.org/10.1002/1521-3773(20011001)40:19%3C3567::AID-ANIE3567%3E3.0.CO;2-C
DOI	10.1002/1521-3773(20011001)40:19<3567::AID-ANIE3567>3.0.CO;2-C
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q74602532
is cites work of	Palladium(II)-catalyzed C-H activation/C-C cross-coupling reactions: versatility and practicality Proline-catalyzed asymmetric reactions Copper-Catalyzed Alkene Diamination: Synthesis of Chiral 2-Aminomethyl Indolines and Pyrrolidines If C-H bonds could talk: selective C-H bond oxidation Copper-catalyzed intermolecular amidation and imidation of unactivated alkanes Synthesis of extended polycyclic aromatic hydrocarbons by oxidative tandem spirocyclization and 1,2-aryl migration Enantioselective functionalization of allylic C-H bonds following a strategy of functionalization and diversification A chiral Lewis acid strategy for enantioselective allylic C-H oxidation The direct arylation of allylic sp(3) C-H bonds via organic and photoredox catalysis Enantioselective cyanation of benzylic C-H bonds via copper-catalyzed radical relay Enantioselective Allylic C-H Oxidation of Terminal Olefins to Isochromans by Palladium(II)/Chiral Sulfoxide Catalysis. Catalytic allylic oxidation of internal alkenes to a multifunctional chiral building block. Catalytic Asymmetric Intermolecular Allylic Functionalization of Unactivated Internal Alkenes. Metal-free direct alkylation of unfunctionalized allylic/benzylic sp3 C-H bonds via photoredox induced radical cation deprotonation Vanadium-Catalyzed C(sp(3))-H Fluorination Reactions Site-specific allylic C-H bond functionalization with a copper-bound N-centred radical A Highly Selective Vanadium Catalyst for Benzylic C-H Oxidation Copper-catalyzed enantioselective Sonogashira-type oxidative cross-coupling of unactivated C(sp3)-H bonds with alkynes Catalytic Allylic Oxidation of Cyclic Enamides and 3,4-Dihydro-2H-Pyrans by TBHP.
is cites work of	wds:Q33732511-C07336AD-F2D2-4F33-B740-5F21DC9212B8 wds:Q42672151-2DC4AC13-EC92-4584-AF0F-883613B3DC48 wds:Q37548669-827078CB-BE6F-40A8-A3A9-97DD6F71329B wds:Q43078980-1CB8523E-C96C-4AB8-A64D-957F7E0D588E wds:Q55692192-ED9D3F16-0A14-4E31-A8C3-6D1B92CD2DBE wds:Q90911590-30978642-B854-4540-8084-CB9EE8D21859 wds:Q37294999-75568EAB-8C77-4A6F-B5BB-EA03DC270534 wds:Q42365644-2AAA3656-6FEF-443C-846F-6E8E77E27D51 wds:Q41926874-03141C30-8F87-4921-826A-588723248BCF wds:Q37853955-AE775147-D2AA-4291-9E3F-F7592A532E07 wds:Q42202343-045BE4BF-6D81-4B68-B1F9-12DA83F9C19B wds:Q47966049-0997CB56-5E54-49A2-865B-8B7782FBD305 wds:Q91933120-16881E58-77ED-461D-B001-439D17E1F197 wds:Q38736922-BA4D9C5A-BD35-4B2F-8C16-A499759FA6A6 wds:Q47148513-A8A0FC17-FDB5-4CFF-9FBC-13246D005ECD wds:Q52599173-CDF943C9-08CE-40BD-8188-21C312F6736B wds:Q41016417-4D8BD35E-9067-44A2-8C60-A0F6A01BB6B9 wds:Q56288501-8D3C1DE3-99DC-4D00-BFBA-984EDCA660E3 wds:Q41013531-F40E7956-9891-4EE5-A9E2-C240A00448F4

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