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
Hauptverfasser: Reddy, Basi V. Subba, Divyavani, Ch, Begum, Zubeda, Yadav, Jhillu S.
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container_issue 40
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container_title ChemInform
container_volume 41
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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source Wiley Online Library - AutoHoldings Journals
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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