Azomethin-Ylide (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "Azomethin-Ylide" in German language version.

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doi.org

  • Iain Coldham, Richard Hufton: Intramolecular Dipolar Cycloaddition Reactions of Azomethine Ylides. In: Chemical Reviews. Band 105, Nr. 7, Juli 2005, S. 2765–2810, doi:10.1021/cr040004c.
  • L. M. Harwood, R. J. Vickers: Azomethine Ylides: Azomethine Ylides. In: Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., New York, USA 2003, ISBN 978-0-471-38726-8, S. 169–252, doi:10.1002/0471221902.ch3.
  • Javier Adrio, Juan C. Carretero: Novel dipolarophiles and dipoles in the metal-catalyzed enantioselective 1,3-dipolar cycloaddition of azomethine ylides. In: Chemical Communications. Band 47, Nr. 24, 2011, S. 6784, doi:10.1039/c1cc10779h.
  • Philippe Dauban, Guillaume Malik: A Masked 1,3-Dipole Revealed from Aziridines. In: Angewandte Chemie International Edition. Band 48, Nr. 48, 16. November 2009, S. 9026–9029, doi:10.1002/anie.200904941.
  • Rolf Huisgen, Wolfgang Scheer, Helmut Huber: Stereospecific Conversion of cis-trans Isomeric Aziridines to Open-Chain Azomethine Ylides. In: Journal of the American Chemical Society. 89. Jahrgang, Nr. 7, 1967, S. 1753–1755, doi:10.1021/ja00983a052.
  • Harold D. Banks: Torquoselectivity Studies in the Generation of Azomethine Ylides from Substituted Aziridines. In: Journal of Organic Chemistry. 75. Jahrgang, Nr. 8, 2010, S. 2510–2517, doi:10.1021/jo902600y, PMID 20329779.
  • Ana L. Cardoso, Teresa M. V. D. Pinho e Melo: Aziridines in Formal [3+2] Cycloadditions: Synthesis of Five-Membered Heterocycles. In: European Journal of Organic Chemistry. 4. Juli 2012, S. n/a–n/a, doi:10.1002/ejoc.201200406.
  • Edward Huie: Intramolecular [3 + 2] cycloaddition routes to carbon-bridged dibenzocycloheptanes and dibenzazepines. In: Journal of Organic Chemistry. 48. Jahrgang, Nr. 18, 1983, S. 2994–2997, doi:10.1021/jo00166a011.
  • Albert Padwa, Henry L. Gingrich, Richard Lim: Regiochemistry of intramolecular munchnone cycloadditions: preparative and mechanistic implications. In: The Journal of Organic Chemistry. Band 47, Nr. 12, Juni 1982, S. 2447–2456, doi:10.1021/jo00133a041.
  • Kendall N. Houk, Javier Gonzalez, Yi Li: Pericyclic Reaction Transition States: Passions and Punctilios, 1935-1995. In: Accounts of Chemical Research. Band 28, Nr. 2, Februar 1995, S. 81–90, doi:10.1021/ar00050a004.
  • Brad R. Henke, Andrew J. Kouklis, Clayton H. Heathcock: Intramolecular 1,3-dipolar cycloaddition of stabilized azomethine ylides to unactivated dipolarophiles. In: The Journal of Organic Chemistry. Band 57, Nr. 26, Dezember 1992, S. 7056–7066, doi:10.1021/jo00052a015.
  • Chuo Chen, Xiaodong Li, Stuart L. Schreiber: Catalytic Asymmetric [3+2] Cycloaddition of Azomethine Ylides. Development of a Versatile Stepwise, Three-Component Reaction for Diversity-Oriented Synthesis. In: Journal of the American Chemical Society. Band 125, Nr. 34, August 2003, S. 10174–10175, doi:10.1021/ja036558z.
  • Javier Adrio, Juan C. Carretero: Novel dipolarophiles and dipoles in the metal-catalyzed enantioselective 1,3-dipolar cycloaddition of azomethine ylides. In: Chemical Communications. Band 47, Nr. 24, 2011, S. 6784, doi:10.1039/c1cc10779h.
  • Wenzhong Gao, Xumu Zhang, Malati Raghunath: Cu(I)-Catalyzed Highly Exo-selective and Enantioselective [3 + 2] Cycloaddition of Azomethine Ylides with Acrylates. In: Organic Letters. Band 7, Nr. 19, September 2005, S. 4241–4244, doi:10.1021/ol0516925.
  • Ichiro Oura, Kenta Shimizu, Kenichi Ogata, Shin-ichi Fukuzawa: Highly Endo-Selective and Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Ylide with α-Enones Catalyzed by a Silver(I)/ThioClickFerrophos Complex. In: Organic Letters. Band 12, Nr. 8, 16. April 2010, S. 1752–1755, doi:10.1021/ol100336q.
  • Philip Allway, Ronald Grigg: Chiral Co(II) and Mn(II) catalysts for the 1,3-dipolar cycloaddition reactions of azomethine ylides derived from arylidene imines of glycine. In: Tetrahedron Letters. Band 32, Nr. 41, Oktober 1991, S. 5817–5820, doi:10.1016/S0040-4039(00)93563-9.
  • Xiao-Hua Chen, Qiang Wei, Shi-Wei Luo, Han Xiao, Liu-Zhu Gong: Organocatalytic Synthesis of Spiro[pyrrolidin-3,3′-oxindoles] with High Enantiopurity and Structural Diversity. In: Journal of the American Chemical Society. Band 131, Nr. 38, 30. September 2009, S. 13819–13825, doi:10.1021/ja905302f.
  • N. A. Nedolya, B. A. Trofimov: [1,7]-Electrocyclization reactions in the synthesis of azepine derivatives. In: Chemistry of Heterocyclic Compounds. Band 49, Nr. 1, April 2013, S. 152–176, doi:10.1007/s10593-013-1236-y.
  • Judit Tóth, András Dancsó, Gábor Blaskó, László Tőke, Paul W. Groundwater: 1,7-Electrocyclization reactions of stabilized α,β:γ,δ-unsaturated azomethine ylides. In: Tetrahedron. Band 62, Nr. 24, Juni 2006, S. 5725–5735, doi:10.1016/j.tet.2006.03.088.
  • Jean-François Eckert, Cyril Bourgogne, Jean-François Nierengarten: An unexpected Diels–Alder reaction on the fullerene core rather than an expected 1,3-dipolar cycloaddition. In: Chemical Communications. Nr. 7, 21. März 2002, S. 712–713, doi:10.1039/b201122k.
  • Barry B. Snider, Yong Ahn, Sean M. O’Hare: Total Synthesis of (±)-Martinellic Acid. In: Organic Letters. Band 3, Nr. 26, Dezember 2001, S. 4217–4220, doi:10.1021/ol016884o.
  • Tomoyuki Onishi, Paul R. Sebahar, Robert M. Williams: Concise, Asymmetric Total Synthesis of Spirotryprostatin A. In: Organic Letters. Band 5, Nr. 17, August 2003, S. 3135–3137, doi:10.1021/ol0351910.
  • Nadia Spiccia, Jose Basutto, Pawel Jokisz, Leon S.-M. Wong, Adam G. Meyer: 1,3-Dipolar Cycloaddition-Decarboxylation Reactions of an Azomethine Ylide with Isatoic Anhydrides: Formation of Novel Benzodiazepinones. In: Organic Letters. Band 13, Nr. 3, 4. Februar 2011, S. 486–489, doi:10.1021/ol102824k.

nih.gov

ncbi.nlm.nih.gov

  • Harold D. Banks: Torquoselectivity Studies in the Generation of Azomethine Ylides from Substituted Aziridines. In: Journal of Organic Chemistry. 75. Jahrgang, Nr. 8, 2010, S. 2510–2517, doi:10.1021/jo902600y, PMID 20329779.