Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/2121
Title: Facile synthesis of alkylidene cyclopentenes via palladium catalyzed ring opening of fulvene derived bicyclic hydrazines
Authors: Anas, S
Sajisha, V S
Jubi John
Nayana Joseph, J
Sholly, C G
Radhakrishnan, K V
Keywords: Pentafulvenes
Alkylidene cyclopentenes
Fulvene
Palladium
Bicyclic hydrazines
Enantioselective total-synthesis
Fischer carbene complexes
Linearly fused tricyclopentanoids
Cycloaddition
Functionalized cyclopentenes
Stereoselective-synthesis
Organoindium reagents
Efficient synthesis
Asymmetric-synthesis
3-oxidopyrylium betaine
Issue Date: 2008
Publisher: Elsevier
Citation: Tetrahedron 64(41):9689-9697;06 Oct 2008
Abstract: A facile synthesis of substituted alkylidene cyclopentenes through a palladium catalyzed ring opening of fulvene derived bicyclic hydrazines with various organometallic reagents is described. The products are versatile synthons with multiple points for functionalization and can be used in the synthesis of a number of biologically active molecules.
URI: http://ir.niist.res.in:8080/jspui/handle/123456789/2121
ISSN: 0040-4020
Appears in Collections:2008

Files in This Item:
File Description SizeFormat 
2008_0156.pdf
  Restricted Access
698.31 kBAdobe PDFView/Open Request a copy


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.