Thank you.
Yes. However, you usually need something to active the silicon, tin, or boron atom. The "literature" is full of this type of reaction, generally conducted on aldehydes.
Please find the link given below.
http://www.arkat-usa.org/get-file/46383/
http://dspace.xmu.edu.cn:8080/dspace/bitstream/handle/2288/10353/BiCl3-Catalyzed%20propargylic%20substitution%20reaction%20of%20propargylic%20alcohols%20with%20C-,%20O-,%20S-%20and%20N-centered%20nucleophiles.pdf?sequence=1
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