Phthalimidesulfenyl chloride - Part 13. 3,3 '-regioselective thiofunctionalization of atropisomeric 2,2 '-biphenols
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 |
الوصف غير متاح. |