A synthesis of (+)-nonactic acid by means of the sulfur-ylide rearrangement

Autor:	Saeko Akimoto, Kazuo Hirayama, Junko Araki, Hirohide Ishige, Toshio Honda, Masayoshi Tsubuki
Rok vydání:	1992
Předmět:	chemistry.chemical_classification Organic Chemistry Condensation Methyl nonactate chemistry.chemical_element Condensation reaction Biochemistry Sulfur Medicinal chemistry Rhodium Catalysis chemistry Ylide Drug Discovery Organic chemistry Enantiomer
Zdroj:	Tetrahedron. 48:79-88
ISSN:	0040-4020
Popis:	(+)-Nonactic acid (1) has been synthesized by employing a condensation of the tetrahydro-2-furanthione (9) with dimethyl α-diazomalonate in the presence of rhodium acetate as a key reaction.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::4dabe84a246fe6df3f4e0a5105319e89 https://doi.org/10.1016/s0040-4020(01)80580-9 Zobrazit plný text záznamu