ChemInform Abstract: Three-Component Reaction of a δ-Hydroxy-α,β-unsaturated Aldehyde with Arylamines and 1,3-Diketones: A Novel Synthesis of Oxa-Aza Bicycles
Perlin aldehyde (I) reacts with β‐enamino ketones or esters, generated in situ, to produce the desired heterobicycles (IV) with high selectivity.
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Veröffentlicht in: | ChemInform 2010-10, Vol.41 (40), p.no-no |
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creator | Reddy, Basi V. Subba Divyavani, Ch Begum, Zubeda Yadav, Jhillu S. |
description | Perlin aldehyde (I) reacts with β‐enamino ketones or esters, generated in situ, to produce the desired heterobicycles (IV) with high selectivity. |
doi_str_mv | 10.1002/chin.201040206 |
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subjects | carbohydrates diastereoselective syntheses diastereoselective syntheses, enantioselective syntheses (incl. cis/trans‐isomerism) enantioselective syntheses (incl. cis/trans-isomerism) multi-membered O multicomponent reactions multi‐membered O,N,S‐heterocycles (with at least 2 different heteroatoms) S-heterocycles (with at least 2 different heteroatoms) |
title | ChemInform Abstract: Three-Component Reaction of a δ-Hydroxy-α,β-unsaturated Aldehyde with Arylamines and 1,3-Diketones: A Novel Synthesis of Oxa-Aza Bicycles |
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