Synthesis of Biaryl Derivatives by Using Ruthenium-Mediated [2+2+2] Cyclotrimerization and Suzuki-Miyaura Cross-Coupling as Key Steps

Please use this identifier to cite or link to this item: http://dspace.library.iitb.ac.in/jspui/handle/100/14307

Title:	Synthesis of Biaryl Derivatives by Using Ruthenium-Mediated [2+2+2] Cyclotrimerization and Suzuki-Miyaura Cross-Coupling as Key Steps
Authors:	KOTHA, S SEEMA, V MOBIN, SM
Keywords:	RING-CLOSING METATHESIS DIELS-ALDER REACTION TRANSITION-METAL-COMPLEXES OLEFIN-METATHESIS ENYNE METATHESIS CLAISEN REARRANGEMENT CATALYTIC METATHESIS ALKYNE CYCLOTRIMERIZATION CYCLOADDITION REACTIONS STRUCTURAL ELUCIDATION
Issue Date:	2011
Publisher:	GEORG THIEME VERLAG KG
Citation:	SYNTHESIS-STUTTGART,(10)1581-1586
Abstract:	Functionalized biaryl derivatives have been prepared by applying [2+2+2] cyclotrimerization with the aid of Grubbs' first-generation catalyst (G-I). The trimerized products were subjected to the Suzuki-Miyaura cross-coupling reaction sequence to generate highly functionalized biaryl derivatives.
URI:	http://dx.doi.org/10.1055/s-0030-1260009 http://dspace.library.iitb.ac.in/jspui/handle/100/14307
ISSN:	0039-7881
Appears in Collections:	Article

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