Please use this identifier to cite or link to this item: http://dspace.library.iitb.ac.in/xmlui/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
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