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Volumn 61, Issue 25, 1996, Pages 9041-9044

Synthesis of highly lodinated icosahedral mono- and dicarbon carboranes

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EID: 0001329148     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo961560c     Document Type: Article
Times cited : (69)

References (36)
  • 1
    • 1542544858 scopus 로고
    • WoliT, M. E., Ed.; John Wiley & Sons, Inc.: New York, Part III, Chapter 61
    • Peng, C. T. In Burger's Medicinal Chemistry, 4th ed.; WoliT, M. E., Ed.; John Wiley & Sons, Inc.: New York, 1981; Part III, Chapter 61, pp 1139-1203.
    • (1981) Burger's Medicinal Chemistry, 4th Ed. , pp. 1139-1203
    • Peng, C.T.1
  • 26
    • 0345350422 scopus 로고
    • Olah, G. E., Ed.; Interscience: New York, Part 2, Chapter XLVI
    • (a) Braendlin, H. P.; McBee, E. T. In Friedel-Crafts and Related Reactions; Olah, G. E., Ed.; Interscience: New York, 1964; Vol. III, Part 2, Chapter XLVI, pp 1517-1593.
    • (1964) Friedel-Crafts and Related Reactions , vol.3 , pp. 1517-1593
    • Braendlin, H.P.1    McBee, E.T.2
  • 34
    • 33646839873 scopus 로고    scopus 로고
    • note
    • N,N-Dimethylamino-l-carbaborane was also periodinated, but a mixture of two compounds was obtained (1:3 ratio by HPLC). Attempts to purify this mixture were unsuccessful. It is likely that the minor product is the monomethyl amine as it is known that demethylation can occur with iodine, and the 'H NMR was consistent with this.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.