Эта публикация цитируется в 2 научных статьях (всего в 2 статьях)
Communications
Reversible intramolecular Dieckmann-type condensation of 2-(2-hydroxymethyl-5,5,6-trimethoxytetrahydropyran-3-ylcarbonyl)-cyclopentanone: an alternative access to medium-sized lactones
Аннотация:
Levoglucosenone-derived 2-[(2S,3S,6S)-2-hydroxymethyl-5,5,6-trimethoxytetrahydro-2H-pyran-3-ylcarbonyl]cyclo-pentanone upon boiling in benzene in the presence of NaH undergoes the retro-Dieckmann-type reaction to afford 10-membered lactone, while storing this reaction mixture at room temperature brings about the starting cyclopentanone derivative. Several structurally analogous compounds were examined in respect of similar transformations.
Образец цитирования:
L. Kh. Faizullina, Yu. S. Galimova, M. Yu. Ovchinnikov, Sh. M. Salikhov, S. L. Khursan, F. A. Valeev, “Reversible intramolecular Dieckmann-type condensation of 2-(2-hydroxymethyl-5,5,6-trimethoxytetrahydropyran-3-ylcarbonyl)-cyclopentanone: an alternative access to medium-sized lactones”, Mendeleev Commun., 29:1 (2019), 64–66
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc1423
https://www.mathnet.ru/rus/mendc/v29/i1/p64
Эта публикация цитируется в следующих 2 статьяx:
L. Kh. Faizullina, A. R. Tagirov, Sh. M. Salikhov, F. A. Valeev, “Ene reaction of Diels–Alder adducts of levoglucosenone and 1,3-dienes with acetaldehyde”, Mendeleev Commun., 33:1 (2023), 9–10
L. Kh. Faizullina, Yu. A. Khalilova, F. A. Valeev, “Intramolecular aldol condensation of Michael adducts of levoglucosenone and cyclododecanone”, Mendeleev Commun., 31:4 (2021), 493–494