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Molecules 2002, 7(8), 674-680; doi:10.3390/70800674
Article

Solid State Deprotection of Acetals and Thioacetals Using Benzyltriphenylphosphonium Peroxymonosulfate

1,* , 1, 2 and 1
1 Pharmaceutical Research Laboratory, College of Chemistry, Isfahan University of Technology, Isfahan 84156, Iran 2 Department of Chemistry, Isfahan University, Isfahan 81744, Iran
* Author to whom correspondence should be addressed.
Received: 17 January 2002 / Revised: 18 August 2002 / Accepted: 21 August 2002 / Published: 31 August 2002
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Abstract

A variety of acetals and thioacetals 2 are deprotected to the corresponding parent carbonyl compounds 3 under solvent-free conditions using benzyltriphenylphosphonium peroxymonosulfate (1) in the presence of aluminum chloride.
Keywords: Acetals; Benzyltriphenylphosphonium peroxymonosulfate; Carbonyl compounds; Thioacetals; Solvent-free deprotection Acetals; Benzyltriphenylphosphonium peroxymonosulfate; Carbonyl compounds; Thioacetals; Solvent-free deprotection
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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MDPI and ACS Style

Hajipour, A.R.; Mallakpour, S.E.; Mohammadpoor-Baltork, I.; Adibi, H. Solid State Deprotection of Acetals and Thioacetals Using Benzyltriphenylphosphonium Peroxymonosulfate. Molecules 2002, 7, 674-680.

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