ChemInform Abstract: Synthesis of Chromen[4,3-b]pyrrolidines by Intramolecular 1,3-Dipolar Cycloadditions of Azomethine Ylides: An Experimental and Computational Assessment of the Origin of Stereocontrol

Reaction of the azomethine ylides, generated from aldehydes (I) or (XI) and α‐amino acids, under conditions A) and B) is investigated.

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Veröffentlicht in:ChemInform 2015-12, Vol.46 (49), p.no-no
Hauptverfasser: Costa, Paulo R. R., Sansano, Jose M., Cossio, Unai, Barcellos, Julio C. F., Dias, Ayres G., Najera, Carmen, Arrieta, Ana, de Cozar, Abel, Cossio, Fernando P.
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container_end_page no
container_issue 49
container_start_page no
container_title ChemInform
container_volume 46
creator Costa, Paulo R. R.
Sansano, Jose M.
Cossio, Unai
Barcellos, Julio C. F.
Dias, Ayres G.
Najera, Carmen
Arrieta, Ana
de Cozar, Abel
Cossio, Fernando P.
description Reaction of the azomethine ylides, generated from aldehydes (I) or (XI) and α‐amino acids, under conditions A) and B) is investigated.
doi_str_mv 10.1002/chin.201549142
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source Wiley Online Library Journals
subjects benzopyran derivatives
cycloaddition reactions
diastereoselective syntheses
diastereoselective syntheses, enantioselective syntheses (incl. cis/trans‐isomerism)
enantioselective syntheses (incl. cis/trans-isomerism)
fused pyrrole derivatives
mechanochemistry
microwave chemistry
microwave chemistry, sonochemistry, mechanochemistry
sonochemistry
title ChemInform Abstract: Synthesis of Chromen[4,3-b]pyrrolidines by Intramolecular 1,3-Dipolar Cycloadditions of Azomethine Ylides: An Experimental and Computational Assessment of the Origin of Stereocontrol
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