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Volumn 66, Issue 31, 2010, Pages 5775-5785

Fluoroalcohols: Versatile solvents in hypervalent iodine chemistry and syntheses of diaryliodonium(III) salts

Author keywords

Diaryliodonium salt; Fluoroalcohol; Hypervalent iodine; Oxidation

Indexed keywords

1,1,1,3,3,3 HEXAFLUOROISOPROPANOL; ALCOHOL DERIVATIVE; CATION; IODINE; ORGANOIODINE DERIVATIVE; PHENYLIODINE BIS TRIFLUOROACETATE; SODIUM CHLORIDE; SOLVENT; TRIFLUOROACETIC ACID; TRIFLUOROETHANOL; UNCLASSIFIED DRUG;

EID: 77955471751     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2010.04.116     Document Type: Article
Times cited : (244)

References (161)
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    • Note
    • 2 under the conditions described in Ref. 21, but afforded a mixture of 6t-OTs and 6t′-OTs or 6u-OTs and 6u′-OTs in low product yields and chemoselectivities.
  • 126
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    • Note
    • In contrast, the corresponding boronic acid did not produce the condensation product 6 and caused the boron-iodine(III) exchange. See, Ref. 20e.
  • 132
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    • Note
    • PhI(OH)OMs was used instead of Koser's reagent to avoid the contamination of the formed polymer with a small amount of p-TsOH.
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    • Note
    • In our measurement, the solubility of the polymer 6al-OMs in MeOH at 25 °C was at least more than 30 mg/mL.
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    • Other reports have appeared after we first introduced the fluoroalcohols for the catalytic utilization of hypervalent iodine reagents. See: A. Moroda, and H. Togo Synthesis 2008 1257
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    • Moroda, A.1    Togo, H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.