As described above.
Show me lit. ref. if there are examples.
Thanks from a boy inaccessible to scifinder o(╥﹏╥)o
Jukka Salminen
This is not a trivial task. You can start by studying this article https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3430791/
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Shaema Kh. Mohamed
You can benefit from this article
https://doi.org/10.1016/j.tet.2006.01.118
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James Demers
Swern oxidation should give you the aldehyde without trouble. Pinnick oxidation is worth a try to get to the acid, although oxidation of the thioether might be competitive. (Chlorite is known to oxidize both substrates.)
If you don't mind adding protection/deprotection steps, it is possible to protect the thioether as a sulfonium salt:
Article Thioether protection via selectively cleavable sulfonium salts
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