2015
DOI: 10.1002/chin.201507250
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ChemInform Abstract: Efficient Synthesis of Eight‐Membered Nitrogen Heterocycles from O‐Propargylic Oximes by Rhodium‐Catalyzed Cascade Reactions.

Abstract: A series of azocine‐1‐oxides (II) is prepared by a Rh‐catalyzed 2,3‐rearrangement/heterocyclization reaction sequence of corresponding O‐propargylic oximes (I).

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“…Optically active oximes undergo the reaction with good levels of chirality transfer (eq 29). 105 Five-membered cyclic nitrones are prepared simply by hydroamination of alkenyl ketoximes mediated by inorganic base, K 3 PO 4 (eq 30). 106 Various five-menbered nitrones can be prepared also from allenyl oximes upon treatment of 2,2dimethylpentane-3,4-dienal oxime with aqueous KOH or with aqueous NH 3 (eq 31).…”
Section: Reaction Of Oximesmentioning
confidence: 99%
“…Optically active oximes undergo the reaction with good levels of chirality transfer (eq 29). 105 Five-membered cyclic nitrones are prepared simply by hydroamination of alkenyl ketoximes mediated by inorganic base, K 3 PO 4 (eq 30). 106 Various five-menbered nitrones can be prepared also from allenyl oximes upon treatment of 2,2dimethylpentane-3,4-dienal oxime with aqueous KOH or with aqueous NH 3 (eq 31).…”
Section: Reaction Of Oximesmentioning
confidence: 99%