Аннотация:
Reaction of ninhydrin with α-mercapto carboxylic acids or the corresponding Bunte salts affords 6’ H-spiro(indene-2,2’ -[1,3]oxa- thiane)-1,3,5’ -triones.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
L. Yu. Ukhin, L. V. Belousova, E. N. Shepelenko, A. S. Morkovnik, “Synthesis of 6’ H-spiro(indene-2,2’ -[1,3]oxathiane)-1,3,5’ -triones”, Mendeleev Commun., 23:6 (2013), 352–353
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc2712
https://www.mathnet.ru/rus/mendc/v23/i6/p352
Эта публикация цитируется в следующих 6 статьяx:
Purak Das, Suvendu Maity, Prasanta Ghosh, Arpita Dutta, Suven Das, “Condensation of ninhydrin with phenols: Regioselective formation of diverse organic scaffolds and crystal structure studies”, Journal of Molecular Structure, 1202 (2020), 127260
Suven Das, “Recent applications of ninhydrin in multicomponent reactions”, RSC Adv., 10:32 (2020), 18875
Pratibha Verma, Ankush Mishra, Swati Chauhan, Sundaram Singh, Vandana Srivastava, “DABCO Catalyzed Synthesis of β‐Hydroxy Ketones Derived from α‐Methyl Ketones and Ninhydrin under Microwave Irradiations”, ChemistrySelect, 4:19 (2019), 5394
Tatsuya Yuki, Morio Yonekawa, Kozo Matsumoto, Yoshihisa Sei, Ikuyoshi Tomita, Takeshi Endo, “Hemithioketal formation of vicinal tricarbonyl compound with thiols and their recovery”, Tetrahedron, 72:32 (2016), 4783
Lev Yu. Ukhin, Lyudmila V. Belousova, Evgenii N. Shepelenko, Anatolii S. Morkovnik, “ChemInform Abstract: Synthesis of 6′ H‐Spiro(indene‐2,2′‐[1,3]oxathiane)‐1,3,5′‐triones.”, ChemInform, 45:18 (2014)
L. O. Khafizova, R. R. Gubaidullin, N. R. Popod'ko, E. S. Meshcheryakova, L. M. Khalilov, U. M. Dzhemilev, “Zirconium-catalyzed one-pot synthesis of ɛ-spirocyclopropyl-ɛ-caprolactones”, Mendeleev Commun., 24:4 (2014), 226–228
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