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1.
Petro P Onys'ko Olena A SuvalovaYuliya V Rassukana Tetyana I ChudakovaAnatolii D Sinitsa 《Tetrahedron letters》2003,44(9):1855-1857
The reaction of alkyl trifluoro(organylsulfonylimino)propionates with phosphites occurs with NC transfer of the RSO2 group and leads to sulfonyl-substituted trifluoroalanine derivatives. The novel rearrangement is interpreted as cheletropic 1,4-cycloaddition of the phosphite and subsequent 1,2-shift of the sulfonyl group in the intermediate cyclic phosphorane. 相似文献
2.
Mohamed R. Mahran Wafaa M. Abdou Maha D. Khidre 《Monatshefte für Chemie / Chemical Monthly》1990,121(1):51-58
Summary The reaction of furil (1) with trialkyl phosphites2 yielded caged phosphorane derivatives of types3a-c. Dry hydrogen chloride gas converted3a-c into the respectivea-hydroxyvinyl-phosphates8a-c which are equally produced by reacting furil with the appropriate dialkyl phosphite7. The reaction of furil with ylide-phosphoranes10 proceeded according to the Wittig reaction mechanism to give the respective ethylenes11a-c. The new compounds have been characterized by their spectroscopic data (IR, PMR,31P-NMR, MS) and elementary analyses.Dedicated to Prof. M. Sidky on the occasion of his 60th birthday 相似文献
3.
T. A. Mastryukova 《Phosphorus, sulfur, and silicon and the related elements》2013,188(1-4):65-68
Abstract The ability of the phosphoryl group to undergo enolization has been studied. The introduction of strongly electronegative substituents at thee α-carbon atom is shown to increase CH- acidity greately and result in the enolization of the P=O group. 相似文献
4.
《Mendeleev Communications》2020,30(1):34-37
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5.
A Sterically Constrained Tricyclic PC3 Phosphine: Coordination Behavior and Insertion of Chalcogen Atoms into P−C Bonds
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Dr. Anne Hentschel M. Sc. Alexander Brand Dr. Philipp Wegener Prof. Dr. Werner Uhl 《Angewandte Chemie (International ed. in English)》2018,57(3):832-835
A tricyclic phosphine has been generated that has a rigid molecular backbone with the P atoms exclusively bound to C(sp2) atoms as well as a very large Tolman angle and buried volume. It is an interesting new ligand in coordination chemistry (Au, Pd complexes) and shows unusual insertion reactions into its endocyclic P?C bonds facilitated by its inherent molecular strain. 相似文献
6.
A method for the synthesis ofO,O-diethyl (N-benzoyl)trichloroacetimidoylphosphonate (1) by successive reaction ofN-(1-diethoxyphosphoryl-2,2-dichlorovinyl)benzamide with Me3SiCl and Cl2 was proposed. The reaction of phosphonate1 with R3P follows the [4+1] cycloaddition mechanism to give phosphoranes, whose stability and further transformations are controlled
by the nature of R.
Dedicated to the memory of Academician M. I. Kabachnik on his 90th birthday.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 10, pp. 2101–2104, October, 1998. 相似文献
7.
Derek P. Gates Ron Rulkens Regina Dirk Paul Nguyen John K. Pudelski Rui Resendes 《Phosphorus, sulfur, and silicon and the related elements》2013,188(1):561-565
Abstract The limits of cyclopentadienyl ring-tilting in [l]ferrocenophanes are explored with the incorporation of group 16 elements and a first row element. In this paper the synthesis and ring-opening polymerisation (ROP) behaviour of highly strained chalcogen-and boron- bridged [l]ferrocenophanes will be described. 相似文献
8.
Davood Aghaei Afshar Mohammad Reza Islami 《Phosphorus, sulfur, and silicon and the related elements》2013,188(9):2238-2246
N-Acetyl-N′-methyl urea or ethyl urea in the presence of an acetylenic ester and a desired phosphine functioned as a NH-acid and added to the triple bond in a chemoselective reaction. One of the obtained products underwent lactonization to the corresponding imidazolidine containing ylide moiety when heated in the presence of a base such as triethyl amine. 相似文献
9.
M. I. Kabachnik T. A. Mastryukova I. M. Aladzheva 《Phosphorus, sulfur, and silicon and the related elements》2013,188(1-3):249-252
Abstract Two new types of tautomerism are discussed: phosphoryl-hydroxyylide and thiophosphoryl-mercaptoylide tautomerism. 相似文献
10.
Vladislava Timofeeva José Miguel Léon Baeza Dr. Raphael Nougué Dr. Mikhail Syroeshkin Prof. Dr. Rene Segundo Rojas Guerrero Dr. Nathalie Saffon-Merceron Dr. Gül Altınbaş Özpınar Dr. Saskia Rathjen Prof. Dr. Thomas Müller Dr. Antoine Baceiredo Dr. Tsuyoshi Kato 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(44):e202201615
A stable (amino)plumbylene-substituted phosphaketene 3 was synthesized by the successive reactions of PbCl2 with two anionic reagents (lithium amidophosphine and NaPCO). Of particular interest, the thermal evolution of 3 , at 80 °C, leads to the transient formation of corresponding amino- and phosphanylidene-phosphaketenes ( 6 and 7 ), via a reductive elimination at the PbII center forming new N−P and P−P bonds. Further evolution of 6 gives a new cyclic (amino)phosphanylidene phosphorane 4 , which shows a unique reactivity as a phosphinidene. This result provides a new synthetic route to phosphinidenes, extending and facilitating further their access. 相似文献