Development and Application of Effective Protocols for the Synthesis of Arylheteroarenes and Biheteroaryls, Including Bioactive Derivatives, by Highly Regioselective Transition Metal-Catalyzed Direct Intermolecular Arylation Reactions of Five-Membered Heteroarenes with (Hetero)aryl Halides

Publisher： Bentham Science Publishers

E-ISSN： 1875-5348|12|9|774-790

ISSN： 1385-2728

Source： Current Organic Chemistry, Vol.12, Iss.9, 2008-06, pp. : 774-790

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

The Construction of Five-Membered Heterocycles by Transition Metal-Catalyzed Cyclization of Propargylic Compounds

By  

Current Organic Chemistry, Vol. 15, Iss. 10, 2011-05 ,pp. : 1625-1643

Bentham Science Publishers

Access to resources Recommend Favorite

Recent Progress Towards Transition-Metal-Catalyzed Direct Arylation of Heteroarenes

By  

Mini-Reviews in Organic Chemistry, Vol. 9, Iss. 1, 2012-02 ,pp. : 87-117

Bentham Science Publishers

Access to resources Recommend Favorite

Metal-catalyzed Heterocyclization: Synthesis of five- and six-membered Nitrogen Heterocycles Through Carbon-Nitrogen Bond Forming Reactions

By  

Current Organic Chemistry, Vol. 15, Iss. 11, 2011-06 ,pp. : 1760-1801

Bentham Science Publishers

Access to resources Recommend Favorite

Cu/Pd-Catalyzed C-2–H Arylation of ­Quinazolin-4(3H)-ones with (Hetero)aryl Halides

By Godeau Julien   Harari Marine   Laclef Sylvain   Deau Emmanuel   Fruit Corinne   Besson Thierry  

European Journal of Organic Chemistry, Vol. 2015, Iss. 35, 2015-12 ,pp. : 7705-7717

Blackwell Publishing

Access to resources Recommend Favorite

Five-membered cyclopalladated complex containing bidentate phosphine ligands; Synthesis, characterization, and highly efficient Suzuki cross-coupling reactions

By SABOUNCHEI SEYYED JAVAD   AHMADI MOHSEN   NASRI ZAHRA  

Journal of Coordination Chemistry, Vol. 66, Iss. 3, 2013-02 ,pp. : 411-423

Taylor & Francis Ltd

Access to resources Recommend Favorite