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N-Heterocyclic Carbene-Catalyzed Oxidation of Unactivated Aldehydes to Esters
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Section:Citing Articles
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This article has been cited by 13 ACS Journal articles (5 most recent appear below).
Total Synthesis of Bryostatin 7 via C–C Bond-Forming Hydrogenation
Yu Lu, Sang Kook Woo, and Michael J. KrischeJournal of the American Chemical Society2011 Article ASAPTotal Synthesis of Bryostatin 7 via C–C Bond-Forming Hydrogenation
Yu Lu, Sang Kook Woo, and Michael J. KrischeJournal of the American Chemical Society2011 Article ASAPThe marine macrolide bryostatin 7 is prepared in 20 steps (longest linear sequence) and 36 total steps with five C–C bonds formed using hydrogenative methods. This approach represents the most concise synthesis of any bryostatin reported, to date.
Enantioselective N-Heterocyclic Carbene-Catalyzed Michael Addition to α,β-Unsaturated Aldehydes by Redox Oxidation
Zi-Qiang Rong, Min-Qiang Jia, and Shu-Li YouOrganic Letters2011 Article ASAPEnantioselective N-Heterocyclic Carbene-Catalyzed Michael Addition to α,β-Unsaturated Aldehydes by Redox Oxidation
Zi-Qiang Rong, Min-Qiang Jia, and Shu-Li YouOrganic Letters2011 Article ASAPEnantioselective N-heterocyclic carbene-catalyzed Michael addition reactions to α,β-unsaturated aldehydes by redox oxidation were realized. With 10 mol % of camphor-derived triazolium salt D, 15 mol % of DBU, 5 mol % of NaBF4, and 100 mol % of quinone ...
NHC-Catalyzed Oxidative Cyclization Reactions of 2-Alkynylbenzaldehydes under Aerobic Conditions: Synthesis of O-Heterocycles
Jong Hyub Park, Sachin V. Bhilare, and So Won YounOrganic Letters2011 13 (9), 2228-2231NHC-Catalyzed Oxidative Cyclization Reactions of 2-Alkynylbenzaldehydes under Aerobic Conditions: Synthesis of O-Heterocycles
Jong Hyub Park, Sachin V. Bhilare, and So Won YounOrganic Letters2011 13 (9), 2228-2231An NHC-catalyzed, regio- and stereoselective oxidative cyclization of o-alkynylbenzaldehydes bearing an unactivated alkyne moiety as an internal electrophile has been developed to afford phthalides and isocoumarins. A single organocatalytic system enabled ...
N-Heterocyclic Carbene-Mediated Oxidative Esterification of Aldehydes: Ester Formation and Mechanistic Studies
Biswajit Maji, Seenuvasan Vedachalan, Xin Ge, Shuting Cai, and Xue-Wei LiuThe Journal of Organic Chemistry2011 76 (9), 3016-3023N-Heterocyclic Carbene-Mediated Oxidative Esterification of Aldehydes: Ester Formation and Mechanistic Studies
Biswajit Maji, Seenuvasan Vedachalan, Xin Ge, Shuting Cai, and Xue-Wei LiuThe Journal of Organic Chemistry2011 76 (9), 3016-3023An unexpected N-heterocyclic carbene-catalyzed esterification of α,β-unsaturated aldehydes including aromatic aldehydes with reactive cinnamyl bromides in the presence of air oxygen or MnO2 as an oxidant is described. In the presence of oxygen, ...
Efficient Catalytic, Oxidative Lactonization for the Synthesis of Benzodioxepinones Using Thiazolium-Derived Carbene Catalysts
Christopher A. Rose and Kirsten ZeitlerOrganic Letters2010 12 (20), 4552-4555Efficient Catalytic, Oxidative Lactonization for the Synthesis of Benzodioxepinones Using Thiazolium-Derived Carbene Catalysts
Christopher A. Rose and Kirsten ZeitlerOrganic Letters2010 12 (20), 4552-4555An efficient, oxidative carbene-catalyzed lactonization reaction has been developed. Using thiazolium precatalysts, a variety of benzodioxepinone products are accessible in good to excellent yields under mild and operationally simple conditions. The ...
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History
- Published In Issue October 02, 2008
- Article ASAPAugust 30, 2008
- Received: August 8, 2008
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