New methods for the arylation of trivalent phosphorus species and Studies towards the synthesis of sesqui-lignan natural products

Chapter one describes two efficient synthesis methods for the preparation of functionalised phosphonium salts. The first method utilises aryl radicals generated by a photo-induced decomposition of diaryliodonium salts, with the second method generating aryl radicals from arylboronic acids and mangan...

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Main Author: Fearnley, Adam
Format: Thesis (University of Nottingham only)
Language:English
Published: 2017
Online Access:https://eprints.nottingham.ac.uk/42420/
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author Fearnley, Adam
author_facet Fearnley, Adam
author_sort Fearnley, Adam
building Nottingham Research Data Repository
collection Online Access
description Chapter one describes two efficient synthesis methods for the preparation of functionalised phosphonium salts. The first method utilises aryl radicals generated by a photo-induced decomposition of diaryliodonium salts, with the second method generating aryl radicals from arylboronic acids and manganese acetate. In both cases a broad substrate scope is demonstrated with respect to both the phosphorus and arylating species. Chapter two describes approaches to the total synthesis of plant sesqui-neolignans. The synthesis of macranthol was achieved in 5 steps from commercially available 4-allylanisole in 7% yield. As well as the first synthesis of the core [4.3.0] ring structure of the fargenin/fargenone family of natural products.
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spelling nottingham-424202025-02-28T13:45:19Z https://eprints.nottingham.ac.uk/42420/ New methods for the arylation of trivalent phosphorus species and Studies towards the synthesis of sesqui-lignan natural products Fearnley, Adam Chapter one describes two efficient synthesis methods for the preparation of functionalised phosphonium salts. The first method utilises aryl radicals generated by a photo-induced decomposition of diaryliodonium salts, with the second method generating aryl radicals from arylboronic acids and manganese acetate. In both cases a broad substrate scope is demonstrated with respect to both the phosphorus and arylating species. Chapter two describes approaches to the total synthesis of plant sesqui-neolignans. The synthesis of macranthol was achieved in 5 steps from commercially available 4-allylanisole in 7% yield. As well as the first synthesis of the core [4.3.0] ring structure of the fargenin/fargenone family of natural products. 2017-07-18 Thesis (University of Nottingham only) NonPeerReviewed application/pdf en arr https://eprints.nottingham.ac.uk/42420/1/Adam%20Fearnley%20Thesis.pdf Fearnley, Adam (2017) New methods for the arylation of trivalent phosphorus species and Studies towards the synthesis of sesqui-lignan natural products. PhD thesis, University of Nottingham.
spellingShingle Fearnley, Adam
New methods for the arylation of trivalent phosphorus species and Studies towards the synthesis of sesqui-lignan natural products
title New methods for the arylation of trivalent phosphorus species and Studies towards the synthesis of sesqui-lignan natural products
title_full New methods for the arylation of trivalent phosphorus species and Studies towards the synthesis of sesqui-lignan natural products
title_fullStr New methods for the arylation of trivalent phosphorus species and Studies towards the synthesis of sesqui-lignan natural products
title_full_unstemmed New methods for the arylation of trivalent phosphorus species and Studies towards the synthesis of sesqui-lignan natural products
title_short New methods for the arylation of trivalent phosphorus species and Studies towards the synthesis of sesqui-lignan natural products
title_sort new methods for the arylation of trivalent phosphorus species and studies towards the synthesis of sesqui-lignan natural products
url https://eprints.nottingham.ac.uk/42420/