Academic Journal

Synthesis of 1,1,4,4‐Tetracyanobuta‐1,3‐Dienes using Tetracyanoethylene Oxide via [3+2]‐Cycloaddition‐Ring Opening Reaction

التفاصيل البيبلوغرافية
العنوان: Synthesis of 1,1,4,4‐Tetracyanobuta‐1,3‐Dienes using Tetracyanoethylene Oxide via [3+2]‐Cycloaddition‐Ring Opening Reaction
المؤلفون: Dar, Arif Hassan, Gowri, Vijayendran, Neethu, K. M., Jayamurugan, Govindasamy
المصدر: ChemistrySelect ; volume 5, issue 40, page 12437-12441 ; ISSN 2365-6549 2365-6549
بيانات النشر: Wiley
سنة النشر: 2020
المجموعة: Wiley Online Library (Open Access Articles via Crossref)
الوصف: Unlike the [3+2] cycloadduct of electron‐donating group (EDG)‐free alkynes with tetracyanoethylene oxide (TCNEO), the EDG induced [3+2] cycloadduct underwent one‐pot ring‐opening and deoxygenation reactions to provide the established EDG‐substituted non‐planar 1,1,4,4‐tetracyanobuta‐1,3‐dienes (TCBDs) push‐pull chromophores. This is an alternate synthetic method that provides access to TCBDs other than the [2+2] cycloaddition–retroelectrocyclization reactions with tetracyanoethene.
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1002/slct.202003179
الاتاحة: http://dx.doi.org/10.1002/slct.202003179
https://onlinelibrary.wiley.com/doi/pdf/10.1002/slct.202003179
https://onlinelibrary.wiley.com/doi/full-xml/10.1002/slct.202003179
Rights: http://onlinelibrary.wiley.com/termsAndConditions#vor
رقم الانضمام: edsbas.6E5CB37A
قاعدة البيانات: BASE