Cyclization of Nitroacetamide Derivatives with a Tethered Phenyl Ring in Triflic Acid

التفاصيل البيبلوغرافية
العنوان: Cyclization of Nitroacetamide Derivatives with a Tethered Phenyl Ring in Triflic Acid
المؤلفون: Jerome Marrot, Jean-Marie Coustard, Bamba Fanté, Sorho Siaka, Yaya Soro
المصدر: Synlett. 25:969-974
بيانات النشر: Georg Thieme Verlag KG, 2014.
سنة النشر: 2014
مصطلحات موضوعية: chemistry.chemical_compound, chemistry, Bicyclic molecule, Organic Chemistry, polycyclic compounds, Cationic polymerization, Intramolecular cyclization, Protonation, Ring (chemistry), Triflic acid, Medicinal chemistry
الوصف: N-(3-Hydroxypropyl)-2-nitro-N-(ω-phenylalkyl)acetami-des underwent intramolecular cyclization in triflic acid to afford the corresponding hydroxyimino six- to nine-membered benzofused lactams. The six-membered derivative slowly transformed into 2-(3-hydroxypropyl)isoquinolin-3-one. NMR spectroscopic analysis in situ provided information on the cationic species involved in the reaction, permitting a mechanism to be postulated. This reaction provides a novel and simple route to benzofused lactams.
تدمد: 1437-2096
0936-5214
DOI: 10.1055/s-0033-1340960
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::8440181c13a0f56d38ae7ca38aa63523
https://doi.org/10.1055/s-0033-1340960
رقم الانضمام: edsair.doi...........8440181c13a0f56d38ae7ca38aa63523
قاعدة البيانات: OpenAIRE
الوصف
تدمد:14372096
09365214
DOI:10.1055/s-0033-1340960