ChemInform Abstract: Diepoxy(15)annulenones Undergo Photochemical Carbonyl-O/Divinyl Ether- O Transportation Rearrangements: Mechanistic Probing of the Rearrangement Sequences Facilitated by 13C/17O NMR Spectroscopy

Autor:	Taiji Imoto, Yuko Kato, Yasuyoshi Nogami, Hideaki Ogawa, Toru Koga, Yuko Ohokubo
Rok vydání:	2010
Předmět:	chemistry.chemical_compound Chemistry mental disorders Ether General Medicine Photochemistry Spectroscopy Annulenone
Zdroj:	ChemInform. 26
ISSN:	0931-7597
DOI:	10.1002/chin.199543077
Popis:	On irradiation, diepoxy[15]annulenone 1 and monobromo-diepoxy[15]annulenone 2 undergo an intriguing rearrangement, whereby all of the ether and carbonyl oxygens of 1 and 2 can travel freely and change their positions in the rings to give 15 position isomers in all.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::33d45ceb0757a35c2002f875a14d889b https://doi.org/10.1002/chin.199543077 Zobrazit plný text záznamu Plný text