Аннотация:
The reaction path in cycloaddition reactions of λ3-iminophosphines with alkoxy- and amino-alkynes depends on the type of starting compound and solvents employed and leads to the formation of phosphirenes or 1,2-diphosphetenes.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
A. D. Averin, N. V. Lukashev, M. A. Kazankova, I. P. Beletskaya, “Phosphirenes and Diphosphetenes: the Products of the Reaction of λ3-lminophosphines with 1-Alkoxy- and 1-Aminoalkynes”, Mendeleev Commun., 3:2 (1993), 68–70
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc5272
https://www.mathnet.ru/rus/mendc/v3/i2/p68
Эта публикация цитируется в следующих 4 статьяx:
Duanghathai Panichakul, François Mathey, “Synthesis, Structure, and Chemistry of 2-Amino-Substituted Phosphirenes”, Organometallics, 28:19 (2009), 5705
M. A. Yurovskaya, “Chemistry of heterocyclic compounds at the Department of Organic Chemistry, Chemical Faculty, M. V. Lomonosov State University. (Review)”, Chem Heterocycl Compd, 41:1 (2005), 24
Annette Ostrowski, Jörg Jeske, Peter G. Jones, Rainer Streubel, “Easy access to C,C′-bifunctionalized 1H-phosphirene–tungsten complexes: evidence for ambiphilic reaction behaviour of a phosphanediyl–tungsten complex”, J. Chem. Soc., Chem. Commun., 1995, no. 24, 2507
A. D. AVERIN, N. V. LUKASHEV, M. A. KAZANKOVA, I. P. BELETSKAYA, “ChemInform Abstract: Phosphirenes and Diphosphetenes: The Products of the Reaction of . lambda.3‐Iminophosphines (I) with 1‐Alkoxy‐ and 1‐Aminoalkynes (II).”, ChemInform, 25:33 (1994)