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Intramolecular Arylation (intramolecular + arylation)
Selected AbstractsChemInform Abstract: Rhodium-Catalyzed Silylation and Intramolecular Arylation of Nitriles via the Silicon-Assisted Cleavage of Carbon,Cyano Bonds.CHEMINFORM, Issue 16 2009Mamoru Tobisu Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source] ChemInform Abstract: Convenient Synthesis of 3-Alkoxy-3-aryloxindoles by Intramolecular Arylation of Mandelic Amides.CHEMINFORM, Issue 52 2008J. Mikael Hillgren Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source] Direct Intramolecular Arylation of Unactivated Arenes: Application to the Synthesis of Aporphine Alkaloids.CHEMINFORM, Issue 18 2005Marc Lafrance Abstract For Abstract see ChemInform Abstract in Full Text. [source] Synthesis of the Dibenzo[f,h]phthalazine and Dibenzo[f,h]cinnoline Skeleton via a "Suzuki,Pd-Catalyzed Intramolecular Arylation" and a "Suzuki,Pschorr" Approach.CHEMINFORM, Issue 44 2003Pal Tapolcsanyi Abstract For Abstract see ChemInform Abstract in Full Text. [source] Evaluation of N -hydroxymethylphthalimide in alkaline medium: Novel entry to the tricyclic [1,3]oxazepine core via an intramolecular , and O -cationic cyclizationJOURNAL OF HETEROCYCLIC CHEMISTRY, Issue 3 2003Armelle Cul Fused isoindolo[1,3]benzo(or thieno)oxazepines 8a,b and one of their positional isomers aromatic tricyclic N,O -acetals 13b are reported to occur efficiently in a three-step sequence from N -hydroxy-methylphthalimide (6). The key step of this methodology is the intramolecular arylation of an endocyclic and/or exocyclic N -acyliminium cation. The mechanism leading to these species, in particular to a tricyclic lactam 13b, is discussed. [source] |