Abstract
A new route to luminescent derivatives of androgenic steroids containing a ketone group in the 3-
or 17-position has been developed. Reaction with the fac-Re(CO)3Cl complex of 3,3’-diamino-2,2’-
bipyridine (complex 1) afforded a cyclic aminal product with different steroids. The rate of reaction
and yield varies according to the conjugation or steric hindrance around the ketone group
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