Arylsulfonyl Group: Activating Properties and Recent Synthetic Applications

التفاصيل البيبلوغرافية
العنوان: Arylsulfonyl Group: Activating Properties and Recent Synthetic Applications
المؤلفون: Marino Petrini, Fabio Martinelli, Alessandro Palmieri
المصدر: Phosphorus, Sulfur, and Silicon and the Related Elements. 186:1032-1045
بيانات النشر: Informa UK Limited, 2011.
سنة النشر: 2011
مصطلحات موضوعية: Inorganic Chemistry, Sulfonyl, chemistry.chemical_classification, Nucleophilic addition, chemistry, Group (periodic table), Stereochemistry, Organic Chemistry, Leaving group, Enantioselective synthesis, Moiety, Biochemistry, Carbanion
الوصف: The carbanion stabilizing effect induced by the arylsulfonyl group has dominated and typified the chemistry of this functional entity for a long time. In addition to this important feature, the activity of the arylsulfonyl moiety as a leaving group has been exploited and a plethora of exciting synthetic applications have been found. The base- or acid-promoted elimination of the sulfonyl group from of α-amido sulfones and sulfonyl indoles is able to produce the in situ generation of reactive N-acylimino and alkylideneindolenine intermediates that can be used in the diastereo and enantioselective synthesis of various amino and heterocyclic compounds.
تدمد: 1563-5325
1042-6507
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eee387ecbe6cd34dce9912116a3f38faTest
https://doi.org/10.1080/10426507.2010.522631Test
حقوق: CLOSED
رقم الانضمام: edsair.doi.dedup.....eee387ecbe6cd34dce9912116a3f38fa
قاعدة البيانات: OpenAIRE