Total Synthesis of (+)-Pleuromutilin

التفاصيل البيبلوغرافية
العنوان: Total Synthesis of (+)-Pleuromutilin
المؤلفون: Felix Schäfers, Sean S. Feng, Elliot P. Farney, Sarah E. Reisman
المصدر: Journal of the American Chemical Society. 140:1267-1270
بيانات النشر: American Chemical Society (ACS), 2018.
سنة النشر: 2018
مصطلحات موضوعية: 010405 organic chemistry, Extramural, Chemistry, Molecular Conformation, Total synthesis, Stereoisomerism, General Chemistry, 010402 general chemistry, Ring (chemistry), 01 natural sciences, Biochemistry, Combinatorial chemistry, Article, Catalysis, 0104 chemical sciences, Stereocenter, chemistry.chemical_compound, Colloid and Surface Chemistry, Stereospecificity, Polycyclic Compounds, Stereoselectivity, Diterpenes, Pleuromutilin
الوصف: An 18-step synthesis of the antibiotic (+)-pleuromutilin is disclosed. The key steps of the synthesis include a highly stereoselective SmI2-mediated cyclization to establish the eight-membered ring, and a stereospecific transannular [1,5]-hydrogen atom transfer to set the C10 stereocenter. This strategy was also used to prepare (+)-12-epi-pleuromutilin. The chemistry described here will enable efforts to prepare new mutilin antibiotics.
وصف الملف: application/pdf; application/zip
تدمد: 1520-5126
0002-7863
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5db7f9f1c42ad5d550c872798ede6aaTest
https://doi.org/10.1021/jacs.7b13260Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....d5db7f9f1c42ad5d550c872798ede6aa
قاعدة البيانات: OpenAIRE