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Volumn 60, Issue 40, 2004, Pages 8855-8860

Reaction of (diacetoxyiodo)benzene with excess of trifluoromethanesulfonic acid. A convenient route to para-phenylene type hypervalent iodine oligomers

Author keywords

(Diacetoxyiodo)benzene; Hypervalent iodine oligomer; para Phenylene structure; Trifluoromethanesulfonic acid

Indexed keywords

(DIACETOXYIODO)BENZENE; BENZENE DERIVATIVE; IODINE DERIVATIVE; OLIGOMER; SODIUM BROMIDE; TRIFLUOROMETHANESULFONIC ACID; UNCLASSIFIED DRUG;

EID: 4444295065     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2004.07.026     Document Type: Article
Times cited : (15)

References (34)
  • 1
    • 4444254504 scopus 로고
    • Patai, S., Rappoport, Z., Eds.; Wiley: New York, Chapters 18 and 25.
    • For recent reviews and books, see: Koser, G. F. In The Chemistry of Functional Groups, Supplement D; Patai, S., Rappoport, Z., Eds.; Wiley: New York, 1983, Chapters 18 and 25.
    • (1983) The Chemistry of Functional Groups, Supplement D
    • Koser, G.F.1
  • 33
    • 4444261222 scopus 로고    scopus 로고
    • Biological evaluations have been conducted at the Agricultural Chemical Research Laboratory of Sumitomo Chemical Co., Ltd., Takarazuka, Japan.
    • Biological evaluations have been conducted at the Agricultural Chemical Research Laboratory of Sumitomo Chemical Co., Ltd., Takarazuka, Japan.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.