ChemInform Abstract: Cycloaddition of a Nitrone to 2-Aminobut-3-en-1-ol for Large-Scale Preparation of 3-Aminopiperidin-4-ols: A New Asymmetric Synthesis of ( 2R,4R,5S)-Tetrahydropseudodistomin

Autor:	Kuniko Fujimoto, Takeaki Naito, Ichiya Ninomiya, Mitsuko Shirakawa, Toshiko Kiguchi, Miho Ikai
Rok vydání:	2010
Předmět:	chemistry.chemical_classification Scale (ratio) Chemistry Enantioselective synthesis Organic chemistry General Medicine Cycloaddition Nitrone
Zdroj:	ChemInform. 25
ISSN:	0931-7597
DOI:	10.1002/chin.199432215
Popis:	Cycloaddition of the nitrone, derived from tetradecanal, to 2-aminobut-3-en-1-ol provides a practical asymmetric synthesis of both (2R,4R,5S)-tetrahydropseudodistomin and all the stereoisomers of racemic tetrahydropseudodistomin.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::aeec997853fcaac0fa0ea2a4d31047a2 https://doi.org/10.1002/chin.199432215 Zobrazit plný text záznamu Plný text