On the selective deprotection of trityl ethers
…, G Hynd, JM Wright, A Sharma
Index: Jones, Graham B.; Hynd, George; Wright, Justin M.; Sharma, Anu Journal of Organic Chemistry, 2000 , vol. 65, # 1 p. 263 - 265
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Citation Number: 37
Abstract
The triphenylmethyl (trityl) protecting group has enjoyed widespread use in contemporary organic synthesis since its original applications in classic carbohydrate chemistry. 1 Its lipophilic nature renders it particularly attractive for the protection of polar water soluble alcohols, including monosaccharides. A variety of methods have been employed for its introduction, including trityl triflate, 2 tritylpyridinium fluoroborate, 3 and the commercially ...
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