112404-79-2Relevant academic research and scientific papers
Efficient method for tetrahydropyranylation/depyranylation of phenols and alcohols using a solid acid catalyst with Wells-Dawson structure
Romanelli, Gustavo P.,Baronetti, Graciela,Thomas, Horacio J.,Autino, Juan C.
, p. 7589 - 7591 (2002)
A simple and efficient procedure to form 2-tetrahydropyranyl acetals of phenols and alcohols is reported. Wells-Dawson heteropolyacid catalyst is used both in bulk form or supported on silica, reaction conditions include room temperature and toluene as solvent. Fast deprotection of THP-acetals can be attained by mere change of the solvent using THF-1% MeOH. In both reactions the supported catalyst is easily recoverable and reusable, and the yields are good to excellent.
Efficient tetrahydropyranylation of phenols and alcohols catalyzed by supported Mo and W Keggin heteropolyacids
Romanelli,Vazquez,Pizzio,Caceres,Blanco,Autino
, p. 1359 - 1365 (2003)
The protection of phenols as tetrahydropyranyl acetals is studied using supported Keggin heteropolyacids as catalysts, specifically molybdophosphoric or tungstophosphoric acids supported on silica. Phenol tetrahydropyranyl acetals are obtained in short times at room temperature with excellent yields. Protection of alcohols is also performed under mild conditions using both supported heteropolyacids, with yields ranging between good and quantitative. The reactions are clean and their workup is very simple. The use of these solid catalysts allows replacing the usual soluble inorganic acids, contributing to waste reduction.
SUBSTITUENT MODIFICATION IN TRI-O-THYMOTIDE AND ITS EFFECTS ON HOST GEOMETRY AND GUEST ENCLATHRATION. 1. SYNTHESIS
Harris, Thomas D.,Oruganti, Subra R.,Davis, Lawrence M.,Keehn, Philip M.,Green, Bernard S.
, p. 1519 - 1540 (2007/10/02)
A new synthesis is described for the preparation of tri-o-thymotide (1, TOT) and some TOT analogues.The methodology is based on the sequential coupling of appropriately substituted and protected salicylic acid monomers followed by cyclization of the deprotected open-chain trimers.A variety of protecting methodologies and coupling sequences are disscussed.The procedure seems generally applicable for the preparation of salicylides and has been used to prepare TOT in 25percent overall yield (for the coupling-deprotection-coupling-deprotection-cyclization sequence).In addition, two new modified TOT-analogues 9 (25percent), and 10 (14percent) were prepared in which the isopropyl group(s) ortho to the phenolic units in TOT is replaced by one (9) or two (10) ethyl groups.A third analogue 66, where the methyl group ortho to the carboxyl group is removed in one of the salicylic acid monomer units of TOT, requires only the last cyclization step for completion of its synthesis.This methodology represents an important breakthrough for the controlled preparation of selected thymotide (salicylide) trimers and allows easy access to a variety of modified thymotides (salicylides) for structural, conformational and host-guest studies.
