Search Results - "Peacock, Lucy R"

Aza-Conjugate Addition Methodology for the Synthesis of N‑Hydroxy-isoindolin-1-ones by Royo, Santiago, Chapman, Robert S. L, Sim, Alisia M, Peacock, Lucy R, Bull, Steven D

“…Aryl-aldehydes containing ortho-substituted propiolate fragments react with hydroxylamine to afford carbinolamine intermediates that undergo intramolecular…”
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Simple aza-conjugate addition methodology for the synthesis of isoindole nitrones and 3,4-dihydroisoquinoline nitrones by Peacock, Lucy R, Chapman, Robert S L, Sedgwick, Adam C, Mahon, Mary F, Amans, Dominique, Bull, Steven D

“…Aryl-aldehydes containing ortho-substituted α,β-unsaturated carboxylic acid derivatives react with hydroxylamine to afford reactive N-hydroxy-carbinolamine…”
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Dihydroxylation-Based Approach for the Asymmetric Syntheses of Hydroxy-γ-butyrolactones by Peed, Jennifer, Davies, Iwan R, Peacock, Lucy R, Taylor, James E, Kociok-Köhn, Gabriele, Bull, Steven D

“…A method of preparing enantiopure hydroxy-γ-butyrolactones containing multiple contiguous stereocenters in high yield with good diastereoselectivity has been…”
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Simple Aza-Conjugate Addition Methodology for the Synthesis of Isoindole Nitrones and 3,4-Dihydro­isoquinoline Nitrones by Peacock, Lucy R, Chapman, Robert S. L, Sedgwick, Adam C, Mahon, Mary F, Amans, Dominique, Bull, Steven D

“…Aryl-aldehydes containing ortho-substituted α,β-unsaturated carboxylic acid derivatives react with hydroxylamine to afford reactive N-hydroxy-carbinolamine…”
Get full text