The rhodium‐catalyzed hydroformylation‐hydrogenation of 1,2‐allenyl‐phosphine oxides and ‐phosphonates is reported in this paper. The regioselectivity was well controlled, affording only saturated linear γ‐phosphinyl aldehydes under the standard conditions: (carbonyl)tris(triphenylphosphine)‐rhodium hydride [RhH(CO)(PPh3)3] (3 mol%), triphenylphosphine (PPh3) (10 mol%), carbon monoxide (CO) (2.4×106 Pa), hydrogen (H2) (subsequently charged to 4.8×106 Pa), toluene, 100 °C, 24 h.
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Guo et al. (2008) studied this question.
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