دورية أكاديمية

A Radical Addition Approach to a Heptafluoro­isopropyl Substituted Arene, Combined with a Highly Diastereoselective Annulation Reaction To Synthesize the Tricyclic Core of BMS-986251

التفاصيل البيبلوغرافية
العنوان: A Radical Addition Approach to a Heptafluoro­isopropyl Substituted Arene, Combined with a Highly Diastereoselective Annulation Reaction To Synthesize the Tricyclic Core of BMS-986251
المؤلفون: William P. Gallagher (1508725), John R. Coombs (1334916), Carlos A. Guerrero (1264551), Eric M. Simmons (2245837), Francisco González-Bobes (1508401)
سنة النشر: 1753
المجموعة: Smithsonian Institution: Digital Repository
مصطلحات موضوعية: Biophysics, Biochemistry, Microbiology, Genetics, Molecular Biology, Physiology, Biotechnology, Evolutionary Biology, Ecology, Immunology, Developmental Biology, Cancer, Computational Biology, Environmental Sciences not elsewhere classified, Biological Sciences not elsewhere classified, Physical Sciences not elsewhere classified, Information Systems not elsewhere classified, perfluoro isopropyl moiety, novel diastereoselective annulation, 3 isolations using, radical addition approach, 10 , radical mechanism, tricyclic core, step installation, single stereoisomer, pyrrolidine ring, new route, asymmetric route, 6 steps
الوصف: We have devised an asymmetric route to the tricyclic core 10 of BMS-986251. The six-step synthesis utilizes readily available starting materials, involves the one-step installation of the perfluoro isopropyl moiety through a radical mechanism, and leverages a novel diastereoselective annulation to build the pyrrolidine ring. Overall, 10 was obtained in 49% yield as a single stereoisomer in 6 steps and 3 isolations using this new route.
نوع الوثيقة: article in journal/newspaper
اللغة: unknown
العلاقة: https://figshare.com/articles/journal_contribution/A_Radical_Addition_Approach_to_a_Heptafluoro_isopropyl_Substituted_Arene_Combined_with_a_Highly_Diastereoselective_Annulation_Reaction_To_Synthesize_the_Tricyclic_Core_of_BMS-986251/16980645Test
DOI: 10.1021/acs.oprd.1c00338.s001
الإتاحة: https://doi.org/10.1021/acs.oprd.1c00338.s001Test
حقوق: CC BY-NC 4.0
رقم الانضمام: edsbas.C834E04C
قاعدة البيانات: BASE