Journal of the Chemical Society. Chemical communications p. 1201 - 1203 (1993)
Update date:2022-09-26
Topics:
Yamamoto, Yoshinori
Asao, Naoki
Meguro, Masaki
Tsukada, Naofumi
Nemoto, Hisao
et al.
Amide cuprate reagents attack the less hindered carbon atom of epoxides to give 1,2-amino alcohols in good yields; this procedure is applied to the synthesis of an aziridine alcohol bearing a carborane framework which is a potentially useful 10B carrier for boron neutron capture therapy.
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