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Synlett 1994; 1994(2): 110-112
DOI: 10.1055/s-1994-22757
DOI: 10.1055/s-1994-22757
letter
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.
Convergent Synthesis of Aminobicyclo[3.3.0]octenes Using Zirconium Chemistry An Unusual Anti-1,3-Amine Shift.
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Publikationsverlauf
Publikationsdatum:
22. März 2002 (online)
Insertion of phenyl isocyanide into zirconacyclopentenes affords iminoacyl complexes which rearrange to give α,β-unsaturated zirconocene η2-imine complexes. These insert alkenes or alkynes to afford elaborated cyclopentenylamines on protic work-up.The products undergo a facile anti-1,3-amine-shift to afford 1-anilinobicyclo[3.3.0]oct-2-enes.