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Volumn 65, Issue 18, 2000, Pages 5514-5521

Preparation, structure, and unique redox properties of mono-, bis-, and tris(diarylmethylene)-1,3,5-trithianes and related compounds

Author keywords

[No Author keywords available]

Indexed keywords

1,3,5 TRITHIANE DERIVATIVE; HETEROCYCLIC COMPOUND; UNCLASSIFIED DRUG;

EID: 0033828414     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo000161l     Document Type: Article
Times cited : (16)

References (28)
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    • p/2 denote the peak potential and half-peak potential, respectively. Myers, R. L.; Shain, I. Anal. Chem. 1969, 41, 980.
    • (1969) Anal. Chem. , vol.41 , pp. 980
    • Myers, R.L.1    Shain, I.2
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    • (a) Nelsen, S. F.; Kessel, C. R. J. Am. Chem. Soc. 1977, 99, 2392. Alder, R. W.; Gill, R.; Goode, N. C. Chem. Commun. 1976, 973. Asmus, K.-D. Acc. Chem. Res. 1979, 12, 436.
    • (1977) J. Am. Chem. Soc. , vol.99 , pp. 2392
    • Nelsen, S.F.1    Kessel, C.R.2
  • 13
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    • (a) Nelsen, S. F.; Kessel, C. R. J. Am. Chem. Soc. 1977, 99, 2392. Alder, R. W.; Gill, R.; Goode, N. C. Chem. Commun. 1976, 973. Asmus, K.-D. Acc. Chem. Res. 1979, 12, 436.
    • (1976) Chem. Commun. , pp. 973
    • Alder, R.W.1    Gill, R.2    Goode, N.C.3
  • 14
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    • (a) Nelsen, S. F.; Kessel, C. R. J. Am. Chem. Soc. 1977, 99, 2392. Alder, R. W.; Gill, R.; Goode, N. C. Chem. Commun. 1976, 973. Asmus, K.-D. Acc. Chem. Res. 1979, 12, 436.
    • (1979) Acc. Chem. Res. , vol.12 , pp. 436
    • Asmus, K.-D.1
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    • (b) Baenziger, N. C.; Buckles, R. E.; Simpson, T. D. J. Am. Chem. Soc. 1967, 89, 3405. Suzuki, T.; Shiohara, H.; Monobe, M.; Sakimura, T.; Tanaka, S.; Yamashita, Y.; Miyashi, T. Angew. Chem., Int. Ed. Engl. 1992, 31, 455.
    • (1967) J. Am. Chem. Soc. , vol.89 , pp. 3405
    • Baenziger, N.C.1    Buckles, R.E.2    Simpson, T.D.3
  • 17
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    • note
    • Such a 2e-process is not surprising when these systems are considered as new examples of the violene/cyanine hybrids (ref 1b).
  • 21
    • 0000171199 scopus 로고
    • Horner, M.; Hünig, S. J. Am. Chem. Soc. 1977, 99, 6122. Freund, W.; Hünig, S. J. Org. Chem. 1987, 52, 2154.
    • (1987) J. Org. Chem. , vol.52 , pp. 2154
    • Freund, W.1    Hünig, S.2
  • 23
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    • Under the EI-MS conditions, 2,4,6-triphenyl-1,3,5-trithiane was reported to undergo skeletal rearrangement by S⋯S bonding: Chattopadhyaya, J. B.; Rao, A. V. R. Org. Mass Spectrom. 1974, 9, 649.
    • (1974) Org. Mass Spectrom. , vol.9 , pp. 649
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    • note
    • 2 although its structure is still ambiguous.
  • 27
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    • note
    • red(AQ) is 1.74, indicating that the 4e-oxidation of 3 in the first process is unlikely.
  • 28
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    • note
    • 3: (the late) Tatsuo Nakamura, Graduate Thesis at the Department of Chemistry, Faculty of Science, Tohoku University, 1995.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.