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A bulk RNA Seq data set is not a single cell RNA data set, and there is no R package that can convert bulk data to single cell data. If you want a single cell data set, you have to do a single cell experiment. Is this a useful activity for a cell line? What are you actually trying to acheive?
To paraphrase another poster here, you are asking how to get a cow out of a steak. You can't do it. A bulk RNASeq experiment does not contain the information about which read came from which cell. No R program can a magically create that information.