Аннотация:
Ninhydrin oxime and mercaptoalkanoic acids in the presence of trifluoroacetic acid form 2,2′-spiranes incorporating indane-1,3-dione and 3-hydroxy-1,3-thiazolidin-4-one or 3-hydroxytetrahydro-1,3-thiazin-4-one moieties. On heating in acetic anhydride, the same reactants undergo replacement of oxime hydroxy group by sulfur thus affording thiooxime-containing alkanoic acids.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
L. Yu. Ukhin, L. G. Kuz'mina, D. V. Alexeenko, L. V. Belousova, E. N. Shepelenko, V. A. Podshibyakin, A. S. Morkovnik, “Novel reactions of ninhydrin oxime with mercaptoalkanoic acids”, Mendeleev Commun., 28:3 (2018), 300–302
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc1745
https://www.mathnet.ru/rus/mendc/v28/i3/p300
Эта публикация цитируется в следующих 6 статьяx:
Azadeh Parhami, Issa Yavari, Gholam Reza Najafi, “A consecutive synthesis of spiro[cyclopenta[b]pyrrole-5,2′-indene] derivatives via spirocyclization/annulation reactions”, Mol Divers, 27:5 (2023), 2001
Jennifer R. Baker, Adam McCluskey, Cecilia C. Russell, Comprehensive Heterocyclic Chemistry IV, 2022, 583
Suven Das, Arpita Dutta, “Ninhydrin Adducts as Valid Synthon in Organic Synthesis: A Review”, ChemistrySelect, 5:36 (2020), 11361
Suven Das, “Recent applications of ninhydrin in multicomponent reactions”, RSC Adv., 10:32 (2020), 18875
L. Yu. Ukhin, L. G. Kuz´mina, D. V. Alexeenko, L. V. Belousova, A. S. Morkovnik, E. N. Shepelenko, V. A. Podshibyakin, G. S. Borodkin, O. I. Dmitrieva, “Novel derivatives of 3,5-di-tert-butylpyrocatechol with pharmacophore substituents”, Russ Chem Bull, 68:12 (2019), 2290
L. Yu. Ukhin, L. G. Kuz'mina, D. V. Alexeenko, L. V. Belousova, A. S. Morkovnik, G. S. Borodkin, T. N. Gribanova, “Uncommon condensations of 1,2,3-triketone 2-oximes with o-phenylenediamine”, Mendeleev Commun., 29:1 (2019), 111–113