Studies toward the total synthesis of allocolchicine, parvifolal A/B & Ru-catalyzed direct arylation of 2-aroylbenzofurans

Paymode, D. J.

dc.contributor.advisor	Ramana, C. V.	en
dc.contributor.author	Paymode, D. J.	en
dc.date.accessioned	2018-09-28T06:58:10Z	en
dc.date.available	2018-09-28T06:58:10Z	en
dc.date.issued	15-12-2017	en
dc.identifier.uri	http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/4347	en
dc.description.abstract	The proposed thesis is divided into three chapters. The first chapter deals with the total synthesis of (±)-allocolchicine and its analogues using cobalt catalyzed alkyne [2 + 2 + 2]-cyclotrimerization along with their biological activity study. The second chapter describes studies toward the total synthesis of resveratrol dimers parvifolal A/B. The third chapter is focused on the ruthenium(II)-catalyzed carbonyl directed arylation of 2- aroylbenzofurans by using arylboronic acids and (hetero)aryltrifluoroborates via C–H bond activation.	en
dc.format.extent	274 p.	en
dc.language.iso	en	en
dc.publisher	CSIR-National Chemical Laboratory, Pune	en
dc.subject	Synthesis of Allocolchicine	en
dc.title	Studies toward the total synthesis of allocolchicine, parvifolal A/B & Ru-catalyzed direct arylation of 2-aroylbenzofurans	en
dc.type	Thesis(Ph.D.)	en
local.division.division	Organic Chemistry Division	en
dc.description.university	AcSIR	en
dc.identifier.accno	TH2341	en