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Collect. Czech. Chem. Commun. 1958, 23, 1126-1132
https://doi.org/10.1135/cccc19581126

Reaktionen der Diazoketone III. Reaktion des Diazoacetons mit Furan und Homologen. Neue einfache Synthese des Octa-3,5-dien-2,7-dions

J. Novák and F. Šorm

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  • Arora Ritu, Kashyap Kriti, Mittal Anshika, Kakkar Rita: Synthesis and Reactions of Diazoketones. Organic Preparations and Procedures International 2019, 51, 103. <https://doi.org/10.1080/00304948.2019.1569409>
  • Lehner Verena, Davies Huw M. L., Reiser Oliver: Rh(II)-Catalyzed Cyclopropanation of Furans and Its Application to the Total Synthesis of Natural Product Derivatives. Org. Lett. 2017, 19, 4722. <https://doi.org/10.1021/acs.orglett.7b02009>
  • Thornton Aaron R., Martin Véronique I., Blakey Simon B.: π-Nucleophile Traps for Metallonitrene/Alkyne Cascade Reactions: A Versatile Process for the Synthesis of α-Aminocyclopropanes and β-Aminostyrenes. J. Am. Chem. Soc. 2009, 131, 2434. <https://doi.org/10.1021/ja809078d>
  • Hedley Simon J., Ventura Dominic L., Dominiak Paulina M., Nygren Cara L., Davies Huw M. L.: Investigation into Factors Influencing Stereoselectivity in the Reactions of Heterocycles with Donor−Acceptor-Substituted Rhodium Carbenoids. J. Org. Chem. 2006, 71, 5349. <https://doi.org/10.1021/jo060779g>
  • Caballero Ana, Díaz-Requejo M. Mar, Trofimenko Swiatoslaw, Belderrain Tomás R., Pérez Pedro J.: Copper-Catalyzed Addition of Ethyl Diazoacetate to Furans:  An Alternative to Dirhodium(II) Tetraacetate. J. Org. Chem. 2005, 70, 6101. <https://doi.org/10.1021/jo050551d>
  • Tranmer Geoffrey K., Capretta Alfredo: Intermolecular carbenoid insertions: Reactions of 2-substituted thiophenes with ethyl diazoacetate in the presence of rhodium (II) acetate. Tetrahedron 1998, 54, 15499. <https://doi.org/10.1016/S0040-4020(98)01018-7>
  • Franck-Neumann Michel, Geoffroy Philippe, Winling Alain: Tricarbonyl iron complexes bearing a free diazo group. II.1 diene and trimethylenemethane diazoketone complexes as precursors of highly reactive ketocarbenes and diazonium cations. Tetrahedron Letters 1995, 36, 8213. <https://doi.org/10.1016/0040-4039(95)01757-9>
  • Nefedov O. M., Saltykova L. E., Vasil'vitskii A. E., Shostakovskii V. M.: Catalytic reaction of sylvan with alkyl diazoacetates as a method for the synthesis of stereoisomeric 4-acetyl-1,3-butadiene-1-carboxylic acids. Russ Chem Bull 1986, 35, 2409. <https://doi.org/10.1007/BF00953375>
  • Wenkert Ernest, Bakuzis Marinalva L. F., Buckwalter Brian L., Woodgate Paul D.: Methyl β-(2-Methyl-5-Oxocyclopentenyl-) Propionate and Ethyl 3-Methyl-6-Oxohepta-2, 4-Dienoate. Synthetic Communications 1981, 11, 533. <https://doi.org/10.1080/00397918108063621>
  • Nefedov O. M., Shostakovskii V. M., Vasil'vitskii A. E., Kravchenko M. I.: Reaction of ethyl diazoacetate with 2-alkenylfurans. Russ Chem Bull 1980, 29, 425. <https://doi.org/10.1007/BF00949628>
  • Nefedov Oleg M., Schostakovsky Viacheslav M., Vasilvizky Alexander E.: Reaktionen von Alkenylfuranen mit Ethyldiazoacetat. Angew. Chem. 1977, 89, 674. <https://doi.org/10.1002/ange.19770890922>
  • Nefedov Oleg M., Shostakovsky Viacheslav M., Vasilvizky Alexander E.: Reaction of Alkenylfurans with Ethyl Diazoacetate. Angew. Chem. Int. Ed. Engl. 1977, 16, 646. <https://doi.org/10.1002/anie.197706462>
  • Franck-Neumann M., Buchecker C.: Photolyse d'acyl-4 et d'acyl-5 pyrazolenines. Acetyl-1 cyclopropenes, vinylcetocarbenes et vinylcetenes. Tetrahedron Letters 1973, 14, 2875. <https://doi.org/10.1016/S0040-4039(01)96075-7>
  • Nefedov O. M., Shostakovskii V. M., Samoilova M. Ya., Kravchenko M. I.: Reaction of furan and its derivatives with ethyl diazoacetate in the presence of copper sulfate. Russ Chem Bull 1972, 21, 2281. <https://doi.org/10.1007/BF00855322>
  • Nefedov O. M., Shostakovskii V. M., Samoilova M. Ya., Kravchenko M. I.: Unusual reaction of alkenylfurans with diazoacetic ester in the presence of copper sulfate. Russ Chem Bull 1971, 20, 1496. <https://doi.org/10.1007/BF00857433>
  • Schiess P., Chia H. L.: Valenzisomerisierung von cis‐Dienonen I. 2‐Vinyl‐3,4,5,6‐tetrahydrobenzaldehyd; Pyrolyse. von 6‐Oxabicyclo [3,1,0] hex‐2‐en [1]. Helvetica Chimica Acta 1970, 53, 485. <https://doi.org/10.1002/hlca.19700530305>
  • Zhdanov Yu.A., Kornilov V.I., Bogdanova G.V.: α-Oxo carbenes of the carbohydrate series. Carbohydrate Research 1966, 3, 139. <https://doi.org/10.1016/S0008-6215(00)82311-3>
  • von E. Doering W., Pomerantz Martin: 2,4-dimethyltricyclo[1.1.1.02,4]pentan-5-one. Tetrahedron Letters 1964, 5, 961. <https://doi.org/10.1016/S0040-4039(00)90414-3>
  • Schenck Günther Otto, Steinmetz Reinhard: Photochemische Bildungsweisen und Umlagerungen von Thiopheno‐ und Furano‐cyclopropancarbonsäureestern. cis,trans‐Muconaldehydsäureester durch Valenzisomerisierung von 2‐Oxa‐bicyclo[3.1.0]hexen‐(3)‐carbonsäure‐(6)‐ester!!. Justus Liebigs Ann. Chem. 1963, 668, 19. <https://doi.org/10.1002/jlac.19636680104>
  • Weygand F., Bestmann H. J.: Neuere präparative Methoden der organischen Chemie III. Synthesen unter Verwendung von Diazoketonen. Angewandte Chemie 1960, 72, 535. <https://doi.org/10.1002/ange.19600721602>