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

Solid State Deprotection of Acetals and Thioacetals Using Benzyltriphenylphosphonium Peroxymonosulfate

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 (CC BY 3.0).

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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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