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Volumn 125, Issue 27, 2003, Pages 8118-8119

From azides to nitro compounds in a few seconds using HOF·CH3CN

Author keywords

[No Author keywords available]

Indexed keywords

1 AZIDOADAMANTANE; 1 AZIDODECANE; 1 NITROADAMANTANE; 4 AZIDONITROBENZENE; 4 METHOXYAZIDOBENZENE; 5 NITROPENTYLACETATE; ALPHA NITROTOLUENE; AZIDE; AZIDOBENZENE; BENZYL AZIDE; CHEMICAL COMPOUND; NITRO DERIVATIVE; NITROBENZENE; NITROCYCLOHEXANE; NITROSOBENZENE; UNCLASSIFIED DRUG;

EID: 0038006070     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja035616d     Document Type: Article
Times cited : (85)

References (27)
  • 23
    • 0038479356 scopus 로고    scopus 로고
    • note
    • 2O. The development of the oxidizing power was monitored by reacting aliquots with acidic aqueous solution of KI. The liberated iodine was then titrated with thiosulfate. Typical concentrations of the oxidizing reagent were around 0.4-0.6 mol/L. With the exception of the [18]O-labeled 11, the final nitro products are known. Their spectral properties are in full agreement with those described in the literature.
  • 25
    • 0014439171 scopus 로고
    • Compound 6 was made previously in 42% yield in a 3-day reaction: Zee-Cheng, K. Y.; Cheng, C. C. J. Med. Chem. 1969, 12, 157.
    • (1969) J. Med. Chem. , vol.12 , pp. 157
    • Zee-Cheng, K.Y.1    Cheng, C.C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.