Benzimidazolylidene carbene ligated palladium catalysis of the Heck reaction in aqueous media

dc.contributor.author	Özdemir, İsmail
dc.contributor.author	Gök, Yetkin
dc.contributor.author	Gürbüz, Nevin
dc.contributor.author	Çetinkaya, Bekir
dc.date.accessioned	2020-06-28T12:02:06Z
dc.date.available	2020-06-28T12:02:06Z
dc.date.issued	2007
dc.identifier.citation	İsmail Ö., Yetkin G., Nevin G., Bekir Ç. (2007). Benzimidazolylidene carbene ligated palladium catalysis of the Heck reaction in aqueous media, Turkish Journal of Chemistry, İnönü Üniversitesi, Malatya.	tr_TR
dc.identifier.uri	http://localhost:8080/xmlui/handle/123456789/16133
dc.description.abstract	Yıl: 2007Cilt: 31Sayı: 4ISSN: 1300-0527Sayfa Aralığı: 397 - 402 Metin Dili:İngilizce Öz: Başlık (İngilizce): Öz (İngilizce):A highly effective, easy to handle and environmentally benign process for a palladium mediated Heck reaction was developed. The in situ prepared 3-component system, Pd(OAc)2/1,3-dialkylbenzimidazolium chlorides (LHX = 1a-g) and Cs2CO3, catalyzes quantitatively the Heck coupling of aryl bromides under mild conditions in aqueous media.	tr_TR
dc.language.iso	en	tr_TR
dc.publisher	Turkish Journal of Chemistry	tr_TR
dc.subject	Mühendislik	tr_TR
dc.subject	Kimya	tr_TR
dc.title	Benzimidazolylidene carbene ligated palladium catalysis of the Heck reaction in aqueous media	tr_TR
dc.type	Article	tr_TR