Phthalimidesulfenyl chloride - Part 13. 3,3 '-regioselective thiofunctionalization of atropisomeric 2,2 '-biphenols

التفاصيل البيبلوغرافية
العنوان: Phthalimidesulfenyl chloride - Part 13. 3,3 '-regioselective thiofunctionalization of atropisomeric 2,2 '-biphenols
المؤلفون: Capozzi, G, Delogu, G, Dettori, MA Fabbri, D, Menichetti, S, Nativi, C, Nuti, R.
المصدر: Tetrahedron letters 40 (1999): 4421–4424. doi:10.1016/S0040-4039(99)00762-5
info:cnr-pdr/source/autori:Capozzi, G ; Delogu, G ; Dettori, MA Fabbri, D ; Menichetti, S ; Nativi, C ; Nuti, R./titolo:Phthalimidesulfenyl chloride-Part 13. 3,3 '-regioselective thiofunctionalization of atropisomeric 2,2 '-biphenols/doi:10.1016%2FS0040-4039(99)00762-5/rivista:Tetrahedron letters/anno:1999/pagina_da:4421/pagina_a:4424/intervallo_pagine:4421–4424/volume:40
بيانات النشر: Pergamon Press, Frankfurt , Regno Unito, 1999.
سنة النشر: 1999
مصطلحات موضوعية: Regioselective reaction, Atropisomeric, Biphenols
الوصف: Regioselective 3,3'-thiofunctionalization of atropisomeric biphenol 2 can be achieved using phthalimidesulfenyl chloride as the key reagent. The bis-thiophthalimide derivative 3 is the starting material for the preparation of linear (7a-d) and macrocyclic (15a-d) C-2 symmetric ligands containing the biphenyl moiety. (C) 1999 Elsevier Science Ltd. All rights reserved.
اللغة: English
URL الوصول: https://explore.openaire.eu/search/publication?articleId=cnr_________::d5a6a65a80b832086b3ffc13d284526a
http://www.cnr.it/prodotto/i/226699
حقوق: OPEN
رقم الأكسشن: edsair.cnr...........d5a6a65a80b832086b3ffc13d284526a
قاعدة البيانات: OpenAIRE