MARKOVNIKOV VINYLBORINATES FROM 9-OXA-10-BORABICYCLO[3.3.2]DECANES

التفاصيل البيبلوغرافية
العنوان: MARKOVNIKOV VINYLBORINATES FROM 9-OXA-10-BORABICYCLO[3.3.2]DECANES
المؤلفون: Karl Matos, John A. Soderquist, Jorge Ramos
المصدر: Tetrahedron Letters. 38:6639-6642
بيانات النشر: Elsevier BV, 1997.
سنة النشر: 1997
مصطلحات موضوعية: Coupling (electronics), chemistry.chemical_classification, Group (periodic table), Chemistry, Organic Chemistry, Drug Discovery, Markovnikov's rule, Biochemistry, Medicinal chemistry, Alkyl
الوصف: Alkylborinates 1 react with α-methoxyvinyllithium (LiAMV) to produce stable “ate” complexes, 2 , which undergo BCl 3 -induced alkyl group migration providing new air-stable vinylborinates, 3 . These intermediates which are readily converted to either unsymmetrical 1,1-disubstituted alkenes ( 7 ) via the Suzuki-Miyaura coupling or, oxidatively, to methyl ketones, ( 8 ), one of which was converted to the antihistaminic drug, metron S, 10 . © 1997 Elsevier Science Ltd.
تدمد: 0040-4039
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::b43ba3bffd59c503e35f360a84a2dcbe
https://doi.org/10.1016/s0040-4039(97)01578-5
حقوق: CLOSED
رقم الأكسشن: edsair.doi...........b43ba3bffd59c503e35f360a84a2dcbe
قاعدة البيانات: OpenAIRE