Stereocontrolled Syntheses of 6-epi-Trehazolin and 6-epi-Trehalamine from D-Ribonolactone

Autor:	Atsushi Kasuya, Masami Arai, Masao Shiozaki, Shuichi Miyamoto, Hideyuki Haruyama, Youji Furukawa, Tomoko Takayama, Yoshiyuki Kobayashi
Rok vydání:	1994
Předmět:	Aminocyclitol Glycosylamine chemistry.chemical_compound chemistry Bicyclic molecule Stereochemistry Organic Chemistry Aldonic acid Structural isomer Absolute configuration Epimer Stereoselectivity
Zdroj:	The Journal of Organic Chemistry. 59:4450-4460
ISSN:	1520-6904 0022-3263
DOI:	10.1021/jo00095a021
Popis:	6-epi-Trehazolin was synthetized in a stereocontrolled manner, and this synthesis proved that an oxazine structural isomer of 6-epi-trehazolin does not exist
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::f9cc00b2335e3324eae2524c0080836f https://doi.org/10.1021/jo00095a021 Zobrazit plný text záznamu