Collect. Czech. Chem. Commun.
1957, 22, 1836-1851
https://doi.org/10.1135/cccc19571836
Reaktionen von Diazoketonen I. Die Reaktion des Diazoacetons mit ungesättigten Verbindungen
J. Novák, J. Ratuský, V. Šneberk and F. Šorm
Crossref Cited-by Linking
- 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>
- Zhang Fuyi, Kulesza Anna, Rani Shikha, Bernet Bruno, Vasella Andrea: 6‐(Diazomethyl)‐1,3‐bis(methoxymethyl)uracil, Synthesis and Transformation into Annulated Pyrimidinediones. Helvetica Chimica Acta 2008, 91, 1201. <https://doi.org/10.1002/hlca.200890132>
- Komissarov I. V., Semenov N. S., Luk'yanenko V. I., Donets V. F., Dolzhenko A. T., Dulenko L. V., Dulenko V. I.: Synthesis and pharmacological properties of derivatives of harman and harmine. Pharm Chem J 1977, 11, 677. <https://doi.org/10.1007/BF00780829>
- Trost Barry M., Kinson Philip L.: On the applicability of the wolff rearrangement to strained hydrocarbons. Tetrahedron Letters 1973, 14, 2675. <https://doi.org/10.1016/S0040-4039(01)96110-6>
- Wenkert Ernest, Buckwalter Brian L., Sathe S. S.: β, γ-Unsaturated Carbonyl Compounds. Synthetic Communications 1973, 3, 261. <https://doi.org/10.1080/00397917308065913>
- Biellmann J.F., Goeldner M.P.: Réactions de l'acide diméthyl-2,6 diacétyl-3,5 dihydro-1,4 pyridine et d'un analogue. Tetrahedron 1971, 27, 1789. <https://doi.org/10.1016/S0040-4020(01)98043-3>
- Mc Murry John E., Glass Thomas E.: A new synthesis of 1,4-diketones: application to the synthesis of -jasmone. Tetrahedron Letters 1971, 12, 2575. <https://doi.org/10.1016/S0040-4039(01)96923-0>
- Hampel Winfried, Kapp Melitta: Reaktionen mit Diazoketonen. X. Synthese von 1,2,3‐Triaroyl‐cyclopropanen und 3,4,5‐Triaroyl‐Δ2‐pyrazolinen. J. Prakt. Chem. 1970, 312, 394. <https://doi.org/10.1002/prac.19703120228>
- Zhdanov Yu.A., Kornilov V.I., Bogdanova G.V.: A new method of synthesis of indolyl glycoses. Carbohydrate Research 1967, 4, 492. <https://doi.org/10.1016/S0008-6215(00)81841-8>
- 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>
- Obata Naruyoshi, Moritani Ichiro: Cyclopropene Derivatives. II. The Reaction of Diazoketone with Triple Bond. Bulletin of the Chemical Society of Japan 1966, 39, 1975. <https://doi.org/10.1246/bcsj.39.1975>
- Doering W.von E., Fossel E.T., Kaye R.L.: Synthesis of tricyclic ketones by copper-catalyzed cyclization of monocyclic olefinic diazoketones. Tetrahedron 1965, 21, 25. <https://doi.org/10.1016/S0040-4020(01)82198-0>
- Moritani Ichiro, Obata Naruyoshi: Syntheses of acylcyclopropene derivatives. Tetrahedron Letters 1965, 6, 2817. <https://doi.org/10.1016/S0040-4039(01)83915-0>
- Huisgen Rolf, Binsch Gerhard, Ghosez Léon: 1.3‐Dipolare Cycloadditionen, VII. Abfangen der Ketocarben‐Zwischenstufe bei der Thermolyse von Diazoketonen. Chem. Ber. 1964, 97, 2628. <https://doi.org/10.1002/cber.19640970930>
- Huisgen R., König H., Binsch G., Sturm H. J.: 1.3‐Dipolare Additionen der Ketocarbene. Angewandte Chemie 1961, 73, 368. <https://doi.org/10.1002/ange.19610731105>
- 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>
