Synthesis of (+)-solenopsin via Pd-catalyzed N-alkylation and cyclization

التفاصيل البيبلوغرافية
العنوان: Synthesis of (+)-solenopsin via Pd-catalyzed N-alkylation and cyclization
المؤلفون: Hidefumi Makabe, Atsushi Kawamura, Kana Suzuki, Yasunao Hattori
المصدر: Bioscience, Biotechnology, and Biochemistry. 85:223-227
بيانات النشر: Informa UK Limited, 2021.
سنة النشر: 2021
مصطلحات موضوعية: Models, Molecular, Alkylation, Double bond, Molecular Conformation, Chemistry Techniques, Synthetic, 010402 general chemistry, Ring (chemistry), 01 natural sciences, Applied Microbiology and Biotechnology, Biochemistry, Medicinal chemistry, Catalysis, Analytical Chemistry, chemistry.chemical_compound, Alkaloids, Solenopsin, Moiety, Molecular Biology, chemistry.chemical_classification, 010405 organic chemistry, Organic Chemistry, Stereoisomerism, General Medicine, 0104 chemical sciences, chemistry, Cyclization, Stereoselectivity, Piperidine, Palladium, Biotechnology
الوصف: Synthesis of (+)-solenopsin, a 2,6-disubstituted piperidine alkaloid, isolated from fire ants (Solenopsis), was achieved. Stereoselective construction of trans-2,6-piperidine ring moiety was performed using palladium-catalyzed cyclization. Chain elongation using Grubbs 2nd catalyst followed by the reduction of double bond and the deprotection of the Cbz group afforded (+)-solenopsin.
تدمد: 1347-6947
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::404f47984227c622f22d089d5df71987
https://doi.org/10.1093/bbb/zbaa014
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....404f47984227c622f22d089d5df71987
قاعدة البيانات: OpenAIRE