CSIR-NCL Digital Repository

Development of novel methodologies in Aryne chemistry and their application in the total synthesis of bioactive natural products

Show simple item record

dc.contributor.advisor Mhaske, Santosh, B
dc.contributor.author Dhokale, Ranjeet , A
dc.date.accessioned 2018-09-28T08:30:03Z
dc.date.available 2018-09-28T08:30:03Z
dc.date.issued 2018-05
dc.identifier.uri http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/4351
dc.description.abstract The present thesis demonstrates a creative exploration of aryne as versatile building blocks to construct new C–C and C–heteroatom bonds for the synthesis of various scaffolds and complex natural products. Chapter 1 describes a brief history of aryne, different methods available for their generation and various types of aryne reactions. Representative examples of insertion, pericyclic, annulation and multicomponent reactions of aryne are described in detail. Chapter 2 deals with our studies on C–C, C–P and C–N bond forming reactions of aryne, which is divided into three sections. Section 1 covers the transition-metal-free C–arylation of malonamide esters. We have achieved a selective mono- or di-arylation and quaternary centre generation using arynes. Section 2 demonstrates a novel process for C–P bond construction to afford aryl phosphonates, -phosphinates and phosphine oxides for the first time using transition-metal-free protocol. Section 3 describes an unusual nucleophilic nitration protocol using aryne chemistry, and the concept has been further extended for the synthesis of ortho-difuntionalized nitro-aromatics via a multicomponent reaction. Chapter 3 describes our studies on the total synthesis of bioactive natural products using aryne in two sections. Section 1 deals with the synthesis of the spiroannulated benzofuran-3-one scaffold of Leptosphaerins C and congeners via insertion reaction of aryne, whereas section 2 covers the study towards the total synthesis of Lycorane family of natural products via cycloaddition reaction of aryne. en_US
dc.format.extent 200 p. en_US
dc.language.iso en en_US
dc.publisher CSIR-National Chemical Laboratory, Pune en_US
dc.subject Aryne chemistry en_US
dc.subject Bioactive Naturalroducts en_US
dc.title Development of novel methodologies in Aryne chemistry and their application in the total synthesis of bioactive natural products en_US
dc.type Thesis(Ph.D.) en_US
local.division.division Organic Chemistry Division en_US
dc.description.university AcSIR en_US
dc.identifier.accno TH2336
local.embargo.lift 31-12-2021

Files in this item

This item appears in the following Collection(s)

Show simple item record