التفاصيل البيبلوغرافية
العنوان:
Oxidative cyclization of γ-alkylidene butenolides. Stereoselective preparation of spirolactones
المؤلفون:
David Clemente-Tejeda , Francisco Bermejo , Raquel Galán Fernández
المصدر:
ARKIVOC, Vol 2012, Iss 9, Pp 171-184 (2012)
بيانات النشر:
ARKAT USA, Inc., 2012.
سنة النشر:
2012
مصطلحات موضوعية:
lcsh:QD241-441 , chemistry.chemical_compound , Oxidative cyclization , Methyl cinnamate , lcsh:Organic chemistry , chemistry , Organic Chemistry , Total synthesis , Stereoselectivity , Medicinal chemistry
الوصف:
A new route to 1,6-dioxaspiro[4.4]non-3-en-2-ones is established by bromoetherification of dihydroxybutenolides. An asymmetric total synthesis of 8-epi-crassalactone D starting from methyl cinnamate has been accomplished.
تدمد:
1551-7012
URL الوصول:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5326593da46cac00f6ae680c35a6c92e https://doi.org/10.3998/ark.5550190.0013.915
حقوق:
OPEN
رقم الأكسشن:
edsair.doi.dedup.....5326593da46cac00f6ae680c35a6c92e
قاعدة البيانات:
OpenAIRE
