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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 31, 2001 - Issue 21
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Original Articles

DESILYLATION OF TBDMS ETHERS OF PHENOLS SUSCEPTIBLE TO POLYMERIZATION

A. S. Suleman Departments of Chemistry, University of Toledo, Toledo, OH, 43606-3390, U.S.A.
,
L. M. V. Tillekeratne Department of Medicinal and Biological Chemistry, College of Pharmacy, University of Toledo, Toledo, OH, 43606-3390, U.S.A.
&
R. A. Hudson Department of Medicinal and Biological Chemistry, College of Pharmacy, University of Toledo, Toledo, OH, 43606-3390, U.S.A.Correspondence[email protected]
Pages 3303-3308 | Received 10 Jan 2001, Published online: 20 Aug 2006

Citations (4)

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Read on this site (1)

NadiaL. D. Cabral, LucianoJ.Hoeltgebaum Thiessen & Bogdan Doboszewski. (2008) Protecting Groups Transfer: Unusual Method of Removal of Tr and Tbdms Groups by Transetherification. Nucleosides, Nucleotides & Nucleic Acids 27:8, pages 931-948.
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Articles from other publishers (3)

Sean M. Kerwin & Jonathan Cha. (2014) A concise synthesis of rooperol and related 1,5-diarylpent-1-en-4-ynes. Tetrahedron Letters 55:1, pages 137-141.
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Elias Arkoudis, Ioannis N. Lykakis, Charis Gryparis & Manolis Stratakis. (2009) Biomimetic Synthesis of Dimeric Metabolite Acremine G via a Highly Regioselective and Stereoselective Diels−Alder Reaction. Organic Letters 11:14, pages 2988-2991.
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A. S. Suleman, L. M. V. Tillekeratne & R. A. Hudson. (2010) ChemInform Abstract: Desilylation of TBDMS Ethers of Phenols Susceptible to Polymerization.. ChemInform 33:3.
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