Tetrahedron Letters p. 4417 - 4420 (1980)
Update date:2022-08-02
Topics:
Williams, David R.
Nishitani, Kiyoshi
Phenylselenenyl chloride reacts with enamines at -110° C to give α-phenylselenoaldehydes, and oxidative elimination yields α,β-unsaturated aldehydes.
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(1950)
