Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/1011
Title: Lewis acid catalyzed synthetic approaches toward unsymmetrical diaryl- and triarylmethanes
Authors: Mahesh, S.
Keywords: Triarylmethanes
Synthesis
Pyrrolizidine alkaloids
Benzyl alcohol
Fused-aryl substrates
Issue Date: 6-Sep-2018
Publisher: IISERM
Abstract: The research work carried out is primarily focused on the Lewis acid catalyzed 5-endo-dig cyclization and/or conjugate addition approaches for the synthesis of unsymmetrical diaryl- and triarylmethanes using 2-(2-enynyl)-pyridines or p-quinone methides (p-QMs) as synthetic precursors.
URI: http://hdl.handle.net/123456789/1011
Appears in Collections:PhD-2011

Files in This Item:
File Description SizeFormat 
PH11088.pdf13.18 MBAdobe PDFView/Open


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

Admin Tools