A One-step and Chemoselective Conversion of Silyl-protected Alcohols into the Corresponding Acetates

DOI: 10.1016/S0040-4039(00)73040-1

Source and publish data:

Tetrahedron Letters p. 2027 - 2030 (1994)

Update date:2022-09-26

Topics:

Authors:

Oriyama, Takeshi

Oda, Mihoko

Gono, Junko

Koga, Gen

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Article abstract of DOI:10.1016/S0040-4039(00)73040-1

A reagent system of acetyl bromide combined with a catalytic amount of tin(II) bromide cleaves readily trialkylsilyl ethers to give the corresponding acetates in high yields under very mild conditions.

Full text of DOI:10.1016/S0040-4039(00)73040-1

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