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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ndltd-bl.uk-oai-ethos.bl.uk-7196142018-11-27T03:20:34ZNew methods for the arylation of trivalent phosphorus species, and, Studies towards the synthesis of sesqui-lignan natural productsFearnley, Adam2017Chapter 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.547QD241 Organic chemistryUniversity of Nottinghamhttps://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.719614http://eprints.nottingham.ac.uk/42420/Electronic Thesis or Dissertation |
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547 QD241 Organic chemistry |
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547 QD241 Organic chemistry Fearnley, Adam New methods for the arylation of trivalent phosphorus species, and, Studies towards the synthesis of sesqui-lignan natural products |
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. |
author |
Fearnley, Adam |
author_facet |
Fearnley, Adam |
author_sort |
Fearnley, Adam |
title |
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_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_sort |
new methods for the arylation of trivalent phosphorus species, and, studies towards the synthesis of sesqui-lignan natural products |
publisher |
University of Nottingham |
publishDate |
2017 |
url |
https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.719614 |
work_keys_str_mv |
AT fearnleyadam newmethodsforthearylationoftrivalentphosphorusspeciesandstudiestowardsthesynthesisofsesquilignannaturalproducts |
_version_ |
1718797179792916480 |