J
Joanne E. Harvey
Researcher at Victoria University of Wellington
Publications - 64
Citations - 690
Joanne E. Harvey is an academic researcher from Victoria University of Wellington. The author has contributed to research in topics: Ring (chemistry) & Cyclopropane. The author has an hindex of 15, co-authored 62 publications receiving 630 citations. Previous affiliations of Joanne E. Harvey include University of York & Victoria University, Australia.
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Total Synthesis of Aigialomycin D Using a Ramberg−Bäcklund/RCM Strategy§
TL;DR: A novel combination of ring-closing metathesis (RCM) and Ramberg-Bäcklund reactions enables the C1'-C2' alkene to be masked as a sulfone during formation of the macrocycle by ring closing meetingathesis at the C7'-C8' olefin, thus avoiding competing formation of a cyclohexene.
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Synthesis of oxepines and 2-branched pyranosides from a d-glucal-derived gem-dibromo-1,2-cyclopropanated sugar.
TL;DR: The conversion of cyclopropane-fused carbohydrates into oxepines is an attractive method for accessing diverse members of the septanoside family of carbohydrate mimetics, and 2-Bromooxepines are obtained through silver(I)-promoted thermal ring expansion of a d-glucal-derived gem-dihalocyclopropanated sugar.
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Highly functionalised organolithium and organoboron reagents for the preparation of enantiomerically pure α-amino acids
Christopher W. Barfoot,Joanne E. Harvey,Martin N. Kenworthy,John Paul Kilburn,Mahmood Ahmed,Richard J. K. Taylor +5 more
TL;DR: In this paper, homochiral, highly functionalised organolithium reagents derived from l -serine have been generated and reacted with electrophiles, and the novel enantiomerically pure adducts thus obtained were then converted, through β-amino alcohols, into novel non-proteinogenic αamino acids.
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Pd-catalyzed allylic alkylation cascade with dihydropyrans: regioselective synthesis of furo[3,2-c]pyrans.
TL;DR: A regioselective palladium-catalyzed allylic alkylation cascade forms furo[3,2-c]pyrans from various cyclic β-dicarbonyl bis-nucleophiles and 3,6-dihydro-2H-pyran bis-electrophiles by combination of allylic carbonate and anomeric siloxy leaving groups in the dihydropyran substrate.
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An overview on chemical derivatization and stability aspects of selected avermectin derivatives.
TL;DR: This coherent review will contribute towards the better understanding of the correlation of chemical processes, stability profile and biological activity; therefore, it will help to design the shelf-life stable formulations containing AVMs.