Cyclopropanation using flow-generated diazo compounds.
暂无分享,去创建一个
Richard J Ingham | Claudio Battilocchio | Joel M Hawkins | Steven V Ley | S. Ley | Richard Ingham | D. N. Tran | C. Battilocchio | J. Hawkins | Ricardo Labes | Nuria M Roda | Duc N Tran | Ricardo Labes | Nuria M. Roda
[1] C. Wiles,et al. Continuous flow reactors: a perspective , 2012 .
[2] Ryan L. Hartman,et al. Deciding whether to go with the flow: evaluating the merits of flow reactors for synthesis. , 2011, Angewandte Chemie.
[3] J. N. Johnston,et al. To protonate or alkylate? Stereoselective Brønsted acid catalysis of C-C bond formation using diazoalkanes. , 2010, Angewandte Chemie.
[4] Flavien Susanne,et al. Continuous flow synthesis. A pharma perspective. , 2012, Journal of medicinal chemistry.
[5] H. Schechter,et al. Advantageous Syntheses of Diazo Compounds by Oxidation of Hydrazones with Lead Tetraacetate in Basic Environments , 1995 .
[6] Claudio Battilocchio,et al. A prototype device for evaporation in batch and flow chemical processes , 2013 .
[7] Jun-ichi Yoshida,et al. A flow-microreactor approach to protecting-group-free synthesis using organolithium compounds. , 2011, Nature communications.
[8] G. Maas,et al. Diazo Compounds: Properties and Synthesis , 2012 .
[9] L. Wojtas,et al. Highly asymmetric intramolecular cyclopropanation of acceptor-substituted diazoacetates by Co(II)-based metalloradical catalysis: iterative approach for development of new-generation catalysts. , 2011, Journal of the American Chemical Society.
[10] G. Maas. New syntheses of diazo compounds. , 2009, Angewandte Chemie.
[11] Steven V Ley,et al. Accelerating spirocyclic polyketide synthesis using flow chemistry. , 2014, Angewandte Chemie.
[12] Claudio Battilocchio,et al. Process Intensification for the Continuous Flow Hydrogenation of Ethyl Nicotinate , 2014 .
[13] T. Jamison,et al. Continuous-flow synthesis of functionalized phenols by aerobic oxidation of Grignard reagents. , 2014, Angewandte Chemie.
[14] Huan Xu,et al. Enantioselective iron-catalyzed intramolecular cyclopropanation reactions. , 2014, Angewandte Chemie.
[15] Ian R. Baxendale,et al. The integration of flow reactors into synthetic organic chemistry , 2013 .
[16] C. Tung,et al. Inside Cover: Graphene‐Supported Ultrafine Metal Nanoparticles Encapsulated by Mesoporous Silica: Robust Catalysts for Oxidation and Reduction Reactions (Angew. Chem. Int. Ed. 1/2014) , 2014 .
[17] Stefan France,et al. Intramolecular donor-acceptor cyclopropane ring-opening cyclizations. , 2014, Chemical Society reviews.
[18] D. Werz,et al. A new golden age for donor-acceptor cyclopropanes. , 2014, Angewandte Chemie.
[19] R. Cox,et al. Diastereoselective synthesis of cyclopropane amino acids using diazo compounds generated in situ. , 2003, The Journal of organic chemistry.
[20] W. A. Donaldson,et al. Synthesis of cyclopropane containing natural products , 2001 .
[21] J. Wegner,et al. Flow Chemistry – A Key Enabling Technology for (Multistep) Organic Synthesis , 2012 .
[22] V. Lindsay,et al. Stereoselective Rh2(S-IBAZ)4-catalyzed cyclopropanation of alkenes, alkynes, and allenes: asymmetric synthesis of diacceptor cyclopropylphosphonates and alkylidenecyclopropanes. , 2013, Journal of the American Chemical Society.
[23] S. Ley,et al. The rapid synthesis of oxazolines and their heterogeneous oxidation to oxazoles under flow conditions. , 2015, Organic & biomolecular chemistry.
[24] M. Baumann,et al. The rapid generation of isothiocyanates in flow , 2013, Beilstein journal of organic chemistry.
[25] Claudio Battilocchio,et al. Flow chemistry as a discovery tool to access sp2–sp3 cross-coupling reactions via diazo compounds† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c4sc03072a Click here for additional data file. , 2014, Chemical science.
[26] V. Rendina,et al. Titration of nonstabilized diazoalkane solutions by fluorine NMR. , 2012, The Journal of organic chemistry.
[27] L. Wessjohann,et al. Biosynthesis and metabolism of cyclopropane rings in natural compounds. , 2003, Chemical reviews.
[28] A. Maguire,et al. Taming hazardous chemistry in flow: the continuous processing of diazo and diazonium compounds. , 2015, Chemistry.
[29] Peter H Seeberger,et al. Continuous-flow synthesis of the anti-malaria drug artemisinin. , 2012, Angewandte Chemie.
[30] James H. Bannock,et al. Controlled multistep synthesis in a three-phase droplet reactor , 2014, Nature Communications.
[31] A. Charette,et al. Stereoselective cyclopropanation reactions. , 2003, Chemical reviews.
[32] Th. Röder. Book review, Modern Catalytic Methods for Organic Synthesis with Diazo Compounds , 1999 .
[33] A. de Meijere,et al. Natural occurrence, syntheses, and applications of cyclopropyl-group-containing alpha-amino acids. 1. 1-aminocyclopropanecarboxylic acid and other 2,3-methanoamino acids. , 2007, Chemical reviews.
[34] M. V. George,et al. Oxidation with metal oxides. III. Oxidation of diamines and hydrazines with manganese dioxide , 1968 .
[35] Steven V Ley,et al. Flow chemistry syntheses of natural products. , 2013, Chemical Society reviews.
[36] J. S. Kingsbury,et al. Synthesis of acyclic ketones by catalytic, bidirectional homologation of formaldehyde with nonstabilized diazoalkanes. Application of a chiral diazomethyl(pyrrolidine) in total syntheses of erythroxylon alkaloids. , 2013, The Journal of organic chemistry.
[37] Xiaolei Fan,et al. Facile stoichiometric reductions in flow: An example of artemisinin , 2012 .
[38] J. Perman,et al. A general and efficient cobalt(II)-based catalytic system for highly stereoselective cyclopropanation of alkenes with α-cyanodiazoacetates. , 2010, Journal of the American Chemical Society.
[39] C. Oliver Kappe,et al. Continuous flow generation and reactions of anhydrous diazomethane using a Teflon AF-2400 tube-in-tube reactor. , 2013, Organic letters.
[40] M. Doyle. Exceptional selectivity in cyclopropanation reactions catalyzed by chiral cobalt(II)-porphyrin catalysts. , 2009, Angewandte Chemie.
[41] I. Hemeon,et al. Manganese dioxide allylic and benzylic oxidation reactions in ionic liquids , 2004 .