About: Autoxydation von Kohlenwasserstoffen, IX. Mitteil.: Über Peroxyde von Benzol-Derivaten

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About: Autoxydation von Kohlenwasserstoffen, IX. Mitteil.: Über Peroxyde von Benzol-Derivaten Goto Sponge NotDistinct Permalink

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rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у квітні 1944 (uk) im April 1944 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q56210587-DD4910C5-D525-4E28-B70D-88F5BC5F94E0
publication date	1944-04-26 00:00:00Z (xsd:dateTime)
author name string	wds:Q56210587-0F86289D-0E46-43CD-A747-191A36E6EEFC wds:Q56210587-7F2CDD7E-A544-43B3-ABD9-06FBBE927239
author name string	Heinrich Hock Shon Lang
rdfs:label	Autoxydation von Kohlenwasserstoffen, IX. Mitteil.: Über Peroxyde von Benzol-Derivaten (en) Autoxydation von Kohlenwasserstoffen, IX. Mitteil.: Über Peroxyde von Benzol-Derivaten (nl)
skos:prefLabel	Autoxydation von Kohlenwasserstoffen, IX. Mitteil.: Über Peroxyde von Benzol-Derivaten (en) Autoxydation von Kohlenwasserstoffen, IX. Mitteil.: Über Peroxyde von Benzol-Derivaten (nl)
name	Autoxydation von Kohlenwasserstoffen, IX. Mitteil.: Über Peroxyde von Benzol-Derivaten (en) Autoxydation von Kohlenwasserstoffen, IX. Mitteil.: Über Peroxyde von Benzol-Derivaten (nl)
title	wds:Q56210587-FF2C9292-3F9B-4094-A544-C787A4EC2DD5
title	Autoxydation von Kohlenwasserstoffen, IX. Mitteil.: Über Peroxyde von Benzol-Derivaten (en)
page(s)	wds:Q56210587-76CD256F-0521-46EA-8B96-3DEDE50ADB6B
page(s)	257-264
instance of	wds:Q56210587-B6BADF4E-21C3-44A4-A370-7DE0A9E39C54
instance of	scholarly article
published in	wds:Q56210587-2DBD3434-3E60-448B-8FEB-3B0146FFB80A
published in	Berichte der Deutschen Chemischen Gesellschaft zu Berlin. Abteilung B, Abhandlungen
issue	wds:Q56210587-90A0ED8C-BD08-4FF0-A047-C8DC7488A22F
volume	wds:Q56210587-A0459742-44BF-4E17-9AC9-6035B4E9509E
issue	3-4
volume	77
DOI	wds:Q56210587-6707CDA5-6A9B-41F2-82E0-C3CB74E0E973
DOI	http://dx.doi.org/10.1002/CBER.19440770321
DOI	10.1002/CBER.19440770321
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56210587
is cites work of	Studies on hydroperoxide-dependent substrate hydroxylation by purified liver microsomal cytochrome P-450 Singlet oxygen in organic synthesis Diversity in mechanisms of substrate oxidation by cytochrome P450 2D6. Lack of an allosteric role of NADPH-cytochrome P450 reductase in catalytic regioselectivity Phosphomolybdic and phosphotungstic acids as efficient catalysts for the synthesis of bridged 1,2,4,5-tetraoxanes from β-diketones and hydrogen peroxide. Mechanistic investigations of the 2-coumaranone chemiluminescence. A vanadyl complex grafted to periodic mesoporous organosilica: a green catalyst for selective hydroxylation of benzene to phenol. Approach for the Preparation of Various Classes of Peroxides Based on the Reaction of Triketones with H2O2: First Examples of Ozonide Rearrangements Rearrangements of organic peroxides and related processes Ferrocene-modified carbon nitride for direct oxidation of benzene to phenol with visible light. Phenol Synthesis of Ferrocene-Modified Carbon Nitride Photocatalysts by Surface Amidation Reaction for Phenol Synthesis Maracin und Maracen: neuartige Ethinylvinylether- bzw.α-Chlordivinylether-Antibiotica ausSorangium cellulosum mit spezifischer Wirkung gegen Mycobakterien Direct oxidation of the C(sp2)-C(sp3) bond from benzyltrimethylsilanes to phenols. Experimental and computational studies on the C-H amination mechanism of tetrahydrocarbazoles via hydroperoxides. Selective one-pot synthesis of various phenols from diarylethanes. The Gomberg century: Free radicals 1900–2000 Proteomic analysis of nitrate-dependent acetone degradation by Alicycliphilus denitrificans strain BC. From alkylarenes to anilines via site-directed carbon-carbon amination Co-catalyzed highly selective C(sp3)-H nitration. Photodecomposition of DDA. Aerobic C-H amination of tetrahydrocarbazole derivatives via photochemically generated hydroperoxides Six Peroxide Groups in One Molecule - Synthesis of Nine-Membered Bicyclic Silyl Peroxides
is cites work of	wds:Q48055947-95A49FB9-D865-404B-873B-8137FA8DDDE8 wds:Q50462508-FE5104C7-72EA-477E-8BF6-BA0549953EE9 wds:Q56586342-94041F5E-FF1F-4A5C-B720-C170C7E19F1A wds:Q64218474-7AE17836-3A24-46FC-9973-091D70B16B73 wds:Q40463993-2A26CB00-0490-47CB-A06B-B40AA07402A3 wds:Q47447804-7FD61A27-1723-4E9B-A066-BC2FAF0A5DBF wds:Q55878060-FE384ED7-F477-445F-AB98-7C3098B7252B wds:Q43710136-75659E1F-3823-4D65-9223-45C333D135CD wds:Q44624628-B9F611E7-EA9C-43AF-8AE2-795AAB2EF5F7 wds:Q53234954-FAF7A1E8-5D6E-40C7-B55D-F1052AF6B69B wds:Q50494640-BE6E6E57-2C09-4233-AC4F-77E788590752 wds:Q57585791-F4DEC200-7862-4B8D-8B73-A395221DEC66 wds:Q58105658-B75576A5-886B-4951-B40A-656A467B7B6A wds:Q26738939-79363509-8FB3-45C7-9A49-38026969CB5A wds:Q39109680-F9B787FB-5872-4073-A4C2-AB0459BD487A wds:Q47907992-1FB0ED45-B242-4AFC-BCA3-20B1A9ABB83E wds:Q54560212-6659ED09-9FF5-4177-A18B-DAE0F48E315B wds:Q41498586-2B65C863-AD92-4334-B37F-E37182C868DC wds:Q57363552-F6992E5B-BF22-4435-8FE5-CD86F7D1835A wds:Q45824336-268B7171-EF0D-48E9-A337-1A7C30909A7F wds:Q57585815-AD39B1F9-9DD1-44C3-955C-338096FACDE3 wds:Q104102851-54E5A2FC-A8A8-4A57-935E-D2808020CF8B

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