Journal of the Chemical Society. Chemical communications p. 984 - 985 (1990)
Update date:2022-08-02
Topics:
Philip, Abraham
Pitner, J. Bruce
Joo, Young J.
Triggle, David J.
Carroll, F. Ivy
(±)-6-Methyl-6-azabicyclo[3.2.1]octan-3-one (1c) was prepared in three steps from 6-oxabicyclo[3.2.1]oct-3-en-7-one, and stereoselective reduction of (1c) provided (±)-6-methyl-6-azabicyclo[3.2.1]octan- 3α-ol (1a); adaptation of the sequence provided the
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