About: Synergistic effect of ketone and hydroperoxide in Brønsted acid catalyzed oxidative coupling reactions

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About: Synergistic effect of ketone and hydroperoxide in Brønsted acid catalyzed oxidative coupling reactions Goto Sponge NotDistinct Permalink

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scientific article published on 22 October 2013

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description	videnskabelig artikel (da) article científic (ca) article scientific (oc) articol științific (ro) articolo scientifico (it) artigo científico (gl) artigo científico (pt) artigo científico (pt-br) artikull shkencor (sq) artikulong pang-agham (tl) artykuł naukowy (pl) bilimsel makale (tr) scienca artikolo (eo) teaduslik artikkel (et) tieteellinen artikkeli (fi) tudományos cikk (hu) vedecký článok (sk) vetenskaplig artikel (sv) vitenskapelig artikkel (nb) vitskapeleg artikkel (nn) vědecký článek (cs) wetenschappelijk artikel (nl) wissenschaftlicher Artikel (de) επιστημονικό άρθρο (el) научна статия (bg) научная статья (ru) научни чланак (sr) מאמר מדעי (he) სამეცნიერო სტატია (ka) บทความทางวิทยาศาสตร์ (th) artikel ilmiah (id) bài báo khoa học (vi) naučni članak (sr-el) мақолаи илмӣ (tg-cyrl) научни чланак (sr-ec) article scientifique (fr) artículu científicu espublizáu en 2013 (ast) 2013 nî lūn-bûn (nan) 2013年の論文 (ja) 2013년 논문 (ko) artículo científico publicado en 2013 (es) наукова стаття, опублікована в жовтні 2013 (uk) 2013年学术文章 (zh-cn) 2013年学术文章 (zh-sg) 2013年学术文章 (zh-hans) 2013年学术文章 (wuu) 2013年学术文章 (zh-my) 2013年學術文章 (zh-hk) 2013年學術文章 (zh-tw) 2013年學術文章 (zh-hant) 2013年學術文章 (yue) 2013年學術文章 (zh-mo) 2013年学术文章 (zh) ২২ অক্টোবর ২০১৩-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ (bn) scientific article published on 22 October 2013 (en) scientific article published on 22 October 2013 (en-ca) scientific article published on 22 October 2013 (en-gb) مقالة علمية نشرت في 22 أكتوبر 2013 (ar)
publication date	wds:Q43680337-D723B4F2-3451-4180-B444-DECDEAF609C3
publication date	2013-10-22 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q43680337-8A885A2B-F1BE-433F-B2F7-2FBCBB97C81F
language of work or name	English
cites work	wds:Q43680337-078F0514-A34A-4A1C-A898-0AA8B58C9323 wds:Q43680337-12E56DF0-D227-49D1-B093-C9F5C97F1AAB wds:Q43680337-1F091F5A-F4F9-4C7D-ADFC-F9007003D639 wds:Q43680337-2A3AAEC6-A99D-4F2F-BDEB-2DC0AA3E8B54 wds:Q43680337-52133C92-506B-4CEA-89BB-5D50CE8E730D wds:Q43680337-5E72D448-13AD-4336-A535-EF19B5AC8D3B wds:Q43680337-6F27AEC2-116F-4A61-A05B-0EF6A8B1329B wds:Q43680337-7A9AAEB5-3829-4D11-95C8-41E15DC75A33 wds:Q43680337-7CB6BB58-8338-4076-A789-CD422FC9BF8E wds:Q43680337-A14F221A-AFCF-44FB-9425-A64F6C3C8B9D wds:Q43680337-A196B043-93CB-453E-9BB2-611C16EFDE35 wds:Q43680337-B41E2BF3-E859-4ACD-93C5-0DE4414E7B66 wds:Q43680337-B59342CC-2D51-41E2-A158-A73998D9274B wds:Q43680337-BEDB44F8-1D56-4CCF-BE72-0FACE1E06EDF wds:Q43680337-CF882F2A-7578-4D06-BCCC-44BDB56FCF52 wds:Q43680337-D55EB055-F2A8-4B2C-B774-61E44505DA4E wds:Q43680337-F414281A-B341-424E-8B47-7203B32E871F
cites work	Unexpected acid catalysis in reactions of peroxyl radicals with phenols A new reagent for direct difluoromethylation Eosin Y catalyzed visible light oxidative C-C and C-P bond formation. Beyond traditional cross couplings: the scope of the cross dehydrogenative coupling reaction Dioxygen-triggered oxidative radical reaction: direct aerobic difunctionalization of terminal alkynes toward β-keto sulfones Versatile hypervalent-iodine(III)-catalyzed oxidations with m-chloroperbenzoic acid as a cooxidant Iodobenzene-catalyzed alpha-acetoxylation of ketones. in situ generation of hypervalent (diacyloxyiodo)benzenes using m-chloroperbenzoic acid Cu-catalyzed cross-dehydrogenative coupling: a versatile strategy for C-C bond formations via the oxidative activation of sp(3) C-H bonds. Ruthenium-catalyzed oxidative cyanation of tertiary amines with hydrogen peroxide and sodium cyanide. Azobisisobutyronitrile initiated aerobic oxidative transformation of amines: coupling of primary amines and cyanation of tertiary amines. Quaternary ammonium (hypo)iodite catalysis for enantioselective oxidative cycloetherification. Organocatalytic asymmetric intermolecular dehydrogenative α-alkylation of aldehydes using molecular oxygen as oxidant. Mild and efficient strontium chloride hexahydrate-catalyzed conversion of ketones and aldehydes into corresponding gem-dihydroperoxides by aqueous H2O2. Synthesis of Geminal Bisperoxides by Acid-Catalyzed Reaction of Acetals and Enol Ethers with tert-Butyl Hydroperoxide To the core of autocatalysis in cyclohexane autoxidation. A facile, metal- and solvent-free, autoxidative coupling of quinolines with indoles and pyrroles Direct functionalization of (un)protected tetrahydroisoquinoline and isochroman under iron and copper catalysis: two metals, two mechanisms
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