ChemInform Abstract: Ring Opening/C-N Cyclization of Activated Aziridines with Carbon Nucleophiles: Highly Diastereo- and Enantioselective Synthesis of Tetrahydroquinolines

The ring opening/cyclization proceeds as a two‐step reaction with high yields.

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Bibliographic Details
Published inChemInform Vol. 42; no. 51; p. no
Main Authors Ghorai, Manas K., Nanaji, Y., Yadav, A. K.
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 20.12.2011
WILEY‐VCH Verlag
Subjects
diastereoselective syntheses
diastereoselective syntheses, enantioselective syntheses (incl. cis/trans‐isomerism)
enantioselective syntheses (incl. cis/trans-isomerism)
fused pyridine derivatives
quinoline derivatives
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Summary:The ring opening/cyclization proceeds as a two‐step reaction with high yields.
Bibliography:ArticleID:CHIN201151138
istex:79053133C09FE0D073FEBAFC1158B0ABBCF7F949
ark:/67375/WNG-MF15BPJ8-B
ISSN:0931-7597
1522-2667
DOI:10.1002/chin.201151138