Literature DB >> 11670236

C-Hydroxydicarba-closo-dodecaboranes.

Ilya Zharov1, Anil Saxena, Josef Michl, Robert D. Miller.   

Abstract

An improved synthesis and a full characterization of all three 12-vertex C-hydroxydicarba-closo-dodecaboranes 1-3 are reported. These inorganic analogues of phenols are highly acidic, but unlike phenols, they are transparent in the near-UV region and are stable to oxidation. The structure of their oxyanions 1a-3a poses an interesting issue of a closo versus a bridged nido form. Also described is an introduction of a functionalized spacer in position 2 of 1 designed to permit incorporation into more complex organic structures.

Entities:  

Year:  1997        PMID: 11670236     DOI: 10.1021/ic970796b

Source DB:  PubMed          Journal:  Inorg Chem        ISSN: 0020-1669            Impact factor:   5.165


  1 in total

1.  Synthesis and evaluation of carbaborane derivatives of indomethacin as cyclooxygenase inhibitors.

Authors:  Matthias Scholz; Anna L Blobaum; Lawrence J Marnett; Evamarie Hey-Hawkins
Journal:  Bioorg Med Chem       Date:  2011-03-27       Impact factor: 3.641

  1 in total

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