Аннотация:
A new one-pot synthesis of 3-R-1H-phospholane oxides (57–65% yield) was implemented by reaction of phosphorus tri- or pentahalides with 3-R-1-aluminacyclopentanes (in situ generated by Zr-catalyzed cycloalumination of alkenes). The products are readily P-vinylated by Cu-promoted reaction with alkynes.
Образец цитирования:
L. K. Dil'mukhametova, T. V. Tyumkina, V. A. D'yakonov, U. M. Dzhemilev, “Zirconium-catalyzed cycloalumination of alkenes in the one-pot synthesis of 3-substituted 1H-phospholane oxides”, Mendeleev Commun., 27:1 (2017), 23–25
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc1883
https://www.mathnet.ru/rus/mendc/v27/i1/p23
Эта публикация цитируется в следующих 6 статьяx:
A. L. Makhamatkhanova, E. Yu. Bulykina, T. V. Tyumkina, “Atom-economical addition of aldehydes to 3-alkyl-1H-phospholane oxides”, Russ Chem Bull, 73:8 (2024), 2332
A. L. Makhamatkhanova, T. V. Tyumkina, V. M. Yanybin, E. A. Paramonov, “3-Substituted 1H-Phospholane Oxides in the Synthesis of 1-Hydroxy- and 1-Mercaptophospholane Oxides”, Russ J Gen Chem, 92:12 (2022), 2640
Samia Guezane Lakoud, Rim Aissa, Regis Guillot, Martial Toffano, Louisa Aribi‐Zouioueche, “Novel One‐Pot Access to Diastereoisomeric Tertiary Phospholanes Oxides by Using Enantiomerically Pure Phospholane Oxides Under Catalyst‐Free Conditions”, ChemistrySelect, 5:1 (2020), 379
S. A. Kondrashova, Yu. S. Ganushevich, S. V. Kharlamov, V. A. Milyukov, Sh. K. Latypov, “NMR study of the Ni complexes based on 1-alkyl-1,2-diphospholes”, Russ Chem Bull, 68:2 (2019), 374
A. V. Shamsieva, K. R. Trigulova, R. R. Fayzullin, V. V. Khrizanforova, Yu. H. Budnikova, E. I. Musina, A. A. Karasik, “Synthesis of water-soluble bis-N,O-chelate nickel(II) complexes based on new ligands – P-pyridyl-containing phospholane oxides”, Russ Chem Bull, 67:7 (2018), 1206
S. F. Malysheva, N. K. Gusarova, N. A. Belogorlova, A. O. Sutyrina, A. I. Albanov, B. G. Sukhov, V. A. Kuimov, Yu. I. Litvintsev, B. A. Trofimov, “Phosphorus halide free synthesis of 1,2,3,4-tetrahydroisophosphinoline 2-oxides”, Mendeleev Commun., 28:1 (2018), 29–30
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