Abstract
The methoxy-group directs entering methoxide ion into the substituted (1 -) position but borohydride attacks chiefly at position 3. Results with malonate and phenyl-lithium are confused by side-reactions and low yields; methyl-lithium causes reductive displacement of the methoxy-group. The results are compared with the behaviour of the metal-free ligand. The methoxycarbonyl group directs methoxide, cyanide, and hydride into the adjacent 2-position, but in the last case some attack at the 4-position is also observed.

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