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Creators/Authors contains: "Wang, Tinghua"

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  1. ; (, Organic & Biomolecular Chemistry)
    Discussed herein is the synthesis of partially protected carbohydrates by manipulating only one type of a protecting group for a given substrate. The first focus of this review is the uniform protection of an unprotected starting material in a way that only one (or two) hydroxyl group remains unprotected. The second focus involves regioselective partial deprotection of uniformly protected compounds in a way that only one (or two) hydroxyl group becomes liberated. 
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  2. ; ; ; ; ; (, Organic & Biomolecular Chemistry)
    null (Ed.)
    In an attempt to refine a CAN-mediated synthesis of 1,3,4,6-tetra- O -acetyl-α- d -glucopyranose (2-OH glucose) we unexpectedly discovered that this reaction proceeds via the intermediacy of glycosyl nitrates. Improved mechanistic understanding of this reaction led to the development of a more versatile synthesis of 2-OH glucose from a variety of precursors. Also demonstrated is the conversion of 2-OH glucose into a variety of building blocks differentially protected at C-2, a position that is generally hard to protect regioselectively in the glucopyranose series. 
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  3. ; ; (, European Journal of Organic Chemistry)
  4. ; ; ; (, European Journal of Organic Chemistry)