Lewis acid catalyzed synthetic approaches toward unsymmetrical diaryl- and triarylmethanes

Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/937

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DC Field	Value	Language
dc.contributor.author	MAHESH, S	-
dc.date.accessioned	2018-11-09T11:34:38Z	-
dc.date.available	2018-11-09T11:34:38Z	-
dc.date.issued	2018-11-09	-
dc.identifier.uri	http://hdl.handle.net/123456789/937	-
dc.description.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.	en_US
dc.description.sponsorship	IISERM	en_US
dc.language.iso	en	en_US
dc.publisher	IISERM	en_US
dc.subject	Triarylmethanes	en_US
dc.subject	Synthesis	en_US
dc.subject	Pyrrolizidine alkaloids	en_US
dc.subject	Benzyl alcohol	en_US
dc.title	Lewis acid catalyzed synthetic approaches toward unsymmetrical diaryl- and triarylmethanes	en_US
dc.type	Thesis	en_US
Appears in Collections:	PHD-2011

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