Аннотация:
The hydrogenation of internal 3,5-diene-1,7-diynes over (η6-naphthalene)tricarbonylchromium affords homoconjugated (Z,Z,Z)-1,4,7-trienes as major products.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
E. P. Serebryakov, A. A. Vasil'ev, D. Yu. Titskii, I. P. Beletskaya, “(η6-Naphthalene)tricarbonylchromium-mediated hydrogenation of 3,5-diene-1,7-diynes as a route to (Z,Z,Z)-1,4,7-trienes”, Mendeleev Commun., 10:5 (2000), 168–170
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc4439
https://www.mathnet.ru/rus/mendc/v10/i5/p168
Эта публикация цитируется в следующих 3 статьяx:
Georgy K. Fukin, Anton V. Cherkasov, Evgeny V. Baranov, Roman V. Rumyantcev, Elena V. Sazonova, Alexander N. Artemov, “The Electron Density Distribution in Crystals of η6–[1,4–dihydrospiro(2H–3,1–benzoxazine–2,1′–cyclohexane)]tricarbonylchromium(0): Experiment vs Molecular Invariom”, ChemistrySelect, 4:37 (2019), 10976
Valentine P. Ananikov, Oleg V. Hazipov, Irina P. Beletskaya, “1,4‐Diiodo‐1,3‐dienes: Versatile Reagents in Organic Synthesis”, Chemistry — An Asian Journal, 6:2 (2011), 306
Edward P. Serebryakov, Andrei A. Vasil'ev, Dmitrii Yu. Titskii, Irina P. Beletskaya, “ChemInform Abstract: (η6‐Naphthalene)tricarbonylchromium‐Mediated Hydrogenation of 3,5‐Diene‐1,7‐diynes as a Route to (Z,Z,Z)‐1,4‐7‐Trienes.”, ChemInform, 32:8 (2001)
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