Lewis acid catalyzed synthetic approaches toward unsymmetrical diaryl- and triarylmethanes

dc.contributor.authorMahesh, S.
dc.date.accessioned2018-09-06T10:37:54Z
dc.date.available2018-09-06T10:37:54Z
dc.date.issued2018-09-06
dc.description.abstractThe 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.provenanceSubmitted by Naresh Naresh (nareshkumar0372@gmail.com) on 2018-09-06T10:37:54Z No. of bitstreams: 1 PH11088 .: 8078 bytes, checksum: a4d8916d512e8e25320de6c393d5af28 (MD5)en
dc.description.provenanceMade available in DSpace on 2018-09-06T10:37:54Z (GMT). No. of bitstreams: 1 PH11088 .: 8078 bytes, checksum: a4d8916d512e8e25320de6c393d5af28 (MD5) Previous issue date: 2018-09-06en
dc.description.sponsorshipIISERMen_US
dc.guideAnand, R.V.
dc.identifier.urihttp://hdl.handle.net/123456789/1011
dc.language.isoenen_US
dc.publisherIISERMen_US
dc.subjectTriarylmethanesen_US
dc.subjectSynthesisen_US
dc.subjectPyrrolizidine alkaloidsen_US
dc.subjectBenzyl alcoholen_US
dc.subjectFused-aryl substratesen_US
dc.titleLewis acid catalyzed synthetic approaches toward unsymmetrical diaryl- and triarylmethanesen_US
dc.typeThesisen_US

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