ChemInform Abstract Oxidations of Alkenes with Hypervalent Iodine Reagents An Alternative Ozonolysis of Phenyl Substituted Alkenes and Allylic Oxidation of Unsubstituted Cyclic Alkenes
Yazarlar (3)
Dr. Öğr. Üyesi Hande USANMAZ Sinop Üniversitesi, Türkiye
Ufuk Atmaca Atatürk Üniversitesi, Türkiye
Murat Çelik
Makale Türü Özgün Makale (SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale)
Dergi Adı TETRAHEDRON LETTERS (Q2)
Dergi ISSN 0040-4039 Dergi Bilgileri (2014)
Dergi Tarandığı Indeksler SSCI
Makale Dili İngilizce Basım Tarihi 04-2014
Kabul Tarihi Yayınlanma Tarihi 01-04-2014
Cilt / Sayı / Sayfa 55 / 14 / 2230–2232 DOI 10.1016/j.tetlet.2014.02.076
Makale Linki http://doi.wiley.com/10.1002/chin.201437043
UAK Araştırma Alanları
Fen Bilimleri ve Matematik
Özet
Unsaturated Cdouble bondC double bonds with a phenyl substituent can be cleaved with iodylbenzene and iodosylbenzene to give carbonyl compounds. It is believed that the reactions occur via a radical pathway. The allylic oxidation of cyclic alkenes lacking a phenyl substituent was achieved in acetonitrile/water mixture (3:1) also using iodylbenzene and iodosylbenzene.
Anahtar Kelimeler
Allylic hydroperoxide | Oxidative cleavage | Hypervalent iodine | Ozonolysis | Alkenes