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Palladium‐Catalyzed [3,3] Sigmatropic Rearrangement of (Allyloxy)iminodiazaphospholidines: Allylic Transposition of CO and CN Functionality
Author(s) -
Lee Ernest E.,
Batey Robert A.
Publication year - 2004
Publication title -
angewandte chemie
Language(s) - German
Resource type - Journals
eISSN - 1521-3757
pISSN - 0044-8249
DOI - 10.1002/ange.200353284
Subject(s) - chemistry , allylic rearrangement , palladium , transposition (logic) , medicinal chemistry , catalysis , stereochemistry , sigmatropic reaction , organic chemistry , philosophy , linguistics
Die thermodynamische Triebkraft der Titelreaktion ist die Umwandlung einer P V N‐ in eine P V O‐Gruppe: Iminodiazaphospholidine 1 liefern Phosphorsäuretriamide 2 , die anschließend unter milden sauren Bedingungen zu (geschützten) primären Aminen 3 hydrolysiert werden. R=Alkyl, Phenyl; Ts= p ‐Toluolsulfonyl.

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