First asymmetric total synthesis of (+)-steganacin determination of absolute stereochemistry

Autor:	Kenji Koga, Kiyoshi Tomioka, Tsuneo Ishiguro
Rok vydání:	1980
Předmět:	chemistry.chemical_compound chemistry Stereochemistry Organic Chemistry Drug Discovery Synthon Steganacin Total synthesis Absolute (perfumery) Biochemistry
Zdroj:	Tetrahedron Letters. 21:2973-2976
ISSN:	0040-4039
DOI:	10.1016/0040-4039(80)88012-9
Popis:	(+)-Steganacin was synthesized in a new and highly specific asymmetric pathway based on the novel application of chiral γ-lactone as a chiral synthon. By this synthesis the absolute stereochemistry of natural (−)-steganacin could be determined in unequivocal way.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::ddfc8d64d5f80407c215782d0a2384ce https://doi.org/10.1016/0040-4039(80)88012-9 Zobrazit plný text záznamu