Did 75% of my Ph.D. on steroid partial synthesis and do know the old literature pretty well but that one is tricky.
Somehow in starting material B the position of the methyl group is illegitimate. Bromo and methyl have to be interchanged.
For the six-membered ring I would follow disco´s way. 2-Step reduction of the naphthol to the corrsponding tetralone, then Robinson Annulation using but-4-en-2-one will give the A, B and C rings (all six-membered). But for the five-membered ring I have no clue so far.