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

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; in revised form: 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

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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.

AMA Style

Hajipour AR, Mallakpour SE, Mohammadpoor-Baltork I, Adibi H. Solid State Deprotection of Acetals and Thioacetals Using Benzyltriphenylphosphonium Peroxymonosulfate. Molecules. 2002; 7(8):674-680.

Chicago/Turabian Style

Hajipour, Abdol R.; Mallakpour, Shadpour E.; Mohammadpoor-Baltork, Iraj; Adibi, Hadi. 2002. "Solid State Deprotection of Acetals and Thioacetals Using Benzyltriphenylphosphonium Peroxymonosulfate." Molecules 7, no. 8: 674-680.

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