3.9 Article

IMPROVED SYNTHESIS OF [closo-1-CB9H10](-) ANION AND NEW C-SUBSTITUTED DERIVATIVES

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INST ORGANIC CHEM AND BIOCHEM
DOI: 10.1135/cccc2008151

关键词

Boranes; Carboranes; Monocarbaborane anions; Weakly coordinating and low nucleophilic anions; Brellochs reaction; Halogenations; Methylations

资金

  1. Ministry of Education, Youth and Sports of the Czech Republic [LC523]
  2. National Science Foundation [CHE-0446688, OISE-0532040]
  3. [ME857]

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The Brellochs method was utilized to gain access to the [closo-1-CB9H10](-) anion (1). Previous work describing the details of the synthesis of 1 via the [closo-2-CB9H10](-) anion (2) was brief and insufficient. Therefore, we report an optimized procedure for the synthesis of 1, the preparation of the unknown C-halogenated series using N-halosuccinimides and bis(benzene-sulfonyl) fluoroamine, and the unknown C-methylated product using CH3I. NMR properties and regularities within the series were also investigated.

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