A total synthesis of 6,7-dihydroeponemycin and determination of stereochemistry of the epoxide ring

التفاصيل البيبلوغرافية
العنوان: A total synthesis of 6,7-dihydroeponemycin and determination of stereochemistry of the epoxide ring
المؤلفون: Toshikazu Oki, Masataka Konishi, Takeshi Ohnuma, Hideaki Hoshi, Shimpei Aburaki
المصدر: Tetrahedron Letters. 34:1047-1050
بيانات النشر: Elsevier BV, 1993.
سنة النشر: 1993
مصطلحات موضوعية: Sharpless epoxidation, chemistry.chemical_compound, Chemistry, Stereochemistry, Organic Chemistry, Drug Discovery, Absolute configuration, Total synthesis, Epoxide, Dihydroeponemycin, Eponemycin, Ring (chemistry), Biochemistry
الوصف: A total synthesis of 6,7-dihydroeponemycin 2 was achieved via the epoxide intermediate 8a . Unresolved absolute configuration of the epoxide ring in 2 and eponemycin 1 was determined to be 2 R by application of the asymmetric Sharpless epoxidation of 9 .
تدمد: 0040-4039
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::239e07c162f640eb1cd300d733a44ae0
https://doi.org/10.1016/s0040-4039(00)77488-0
حقوق: CLOSED
رقم الأكسشن: edsair.doi...........239e07c162f640eb1cd300d733a44ae0
قاعدة البيانات: OpenAIRE