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Cross Coupling Reaction (cross + coupling_reaction)
Selected AbstractsChemInform Abstract: Synthesis of Highly Functionalized 2-(Substituted Biphenyl) Benzimidazole via Suzuki,Miyaura Cross Coupling Reaction.CHEMINFORM, Issue 12 2008Ramanatham Vinodkumar 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] Palladium and Phase Transfer Catalyzed Heck Cross Coupling Reaction in Water under Microwave Irradiation.CHEMINFORM, Issue 39 2002Jin-Xian Wang Abstract For Abstract see ChemInform Abstract in Full Text. [source] ChemInform Abstract: First Examples of a Tosylate in the Palladium-Catalyzed Heck Cross Coupling Reaction.CHEMINFORM, Issue 16 2002Xiaoyong Fu Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 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] A Highly Efficient Synthesis of a Naphthalenoid Histamine-3 AntagonistADVANCED SYNTHESIS & CATALYSIS (PREVIOUSLY: JOURNAL FUER PRAKTISCHE CHEMIE), Issue 11-12 2009Yi-Yin Ku Abstract A highly efficient synthesis of the potent and selective histamine-3 receptor antagonist 1A was accomplished in four chemical steps and a salt formation step in 36% overall yield from 6-bromo-2-naphthalenol 9. The key features are a regioselective Suzuki coupling protocol for selective vinylation of 12 with potassium vinyltrifluoroborate in high yield (92%) with excellent regioselectivity (90:2) and a base-catalyzed hydroamination reaction of 11 in an anti-Markovnikov fashion under mild reaction conditions. An optimized copper-catalyzed cross coupling reaction is used to incorporate the pyridazinone 4. [source] |