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General combinatorial synthesis of tertiary amines on solid support. A novel conditional release strategy based on traceless linking at nitrogen

✍ Scribed by Magnus Gustafsson; Roger Olsson; Carl-Magnus Andersson


Book ID
104211446
Publisher
Elsevier Science
Year
2001
Tongue
French
Weight
105 KB
Volume
42
Category
Article
ISSN
0040-4039

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✦ Synopsis


A novel solid phase synthesis of tertiary amines involving iodide-induced cleavage of the N O bond of resin bound alkoxyammonium intermediates is described. The quaternary intermediates were assembled via sequential reductive aminations followed by alkylation. Cleavage from the solid support was induced by iodide ion or base, to afford the target tertiary amines in excellent purity.