ChemInform Abstract: A Stereoselective Hydroamination Transform to Access Polysubstituted Indolizidines

The indolizines are accessed from simple dieneamines by an intramolecular, diastereo‐, regio‐, and chemoselective directed hydroboration/oxidative migration strategy.

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Bibliographic Details
Published inChemInform Vol. 43; no. 25; p. no
Main Authors Pronin, Sergey V., Tabor, M. Greg, Jansen, Daniel J., Shenvi, Ryan A.
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 19.06.2012
WILEY‐VCH Verlag
Wiley Subscription Services, Inc
Subjects
alkaloids
diastereoselective syntheses
diastereoselective syntheses, enantioselective syntheses (incl. cis/trans‐isomerism)
enantioselective syntheses (incl. cis/trans-isomerism)
fused pyridine derivatives
ring closure reactions
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Summary:The indolizines are accessed from simple dieneamines by an intramolecular, diastereo‐, regio‐, and chemoselective directed hydroboration/oxidative migration strategy.
Bibliography:istex:296787540BE4240E51712B2BB7419D05C8898BDE
ArticleID:CHIN201225167
ark:/67375/WNG-Q2W3TMF6-9
ISSN:0931-7597
1522-2667
DOI:10.1002/chin.201225167