Journal of the Chemical Society. Chemical communications p. 2321 - 2322 (1995)
Update date:2022-08-11
Topics:
Nishibayashi, Yoshiaki
Srivastava, Sanjay Kumar
Takada, Hiroya
Fukuzawa, Shin-ichi
Uemura, Sakae
Asymmetric intramolecular selenocyclisation of alkenoic acids, alkenols and olefinic urethanes using chiral ferrocenylselenenyl cations proceeds smoothly to give the corresponding lactones, cyclic ethers and nitrogen-heterocyclic compounds, respectively, in moderate yields with very high diastereoselectivities.
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