Dehydrohalogenation via (heterogenic) Palladium catalysis is well known to the experienced chemist - "state of the art". No papers have to be cited for that.
I agree with this. I was not clear in my past post. I should have stated that I was unaware of any catalytic reductions of vinyl bromides to bromoalkanes as precedence for your reaction.
Let me try to explain my thinking again. If you reacted acetic acid with phosgene and got acetyl chloride, I would not put that reaction as a failed attempt to make pyruvyl chloride. No one would expect pyruvyl chloride as the product. If you put it in, you would expose a line of thinking that needs explanation or reveals a lack of knowledge. If there was literature to suggest that pyruvyl chloride should be expected, then I might think differently (but probably not with this example).
Nothing has made me think you should obtain a bromoalkane as the product. Will anyone reading your thesis think that should have been the product? In what way is this a contribution to science? If no contribution is being made, why are you reporting it?