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Volumn , Issue 14, 1989, Pages 916-919

Synthesis of the esperamicin A1/calicheamicin γ-trisulphide functionality: Thermal stability and reduction

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EID: 37049086057     PISSN: 00224936     EISSN: None     Source Type: Journal    
DOI: 10.1039/C39890000916     Document Type: Article
Times cited : (43)

References (32)
  • 4
    • 0023820894 scopus 로고
    • For a study on the cleavage of double-stranded DNA
    • For a study on the cleavage of double-stranded DNA,: N. Zein, A. M. Sinha, W. J. McGahren, and G. A. Ellestad, Science, 1988, 240, 1198.
    • (1988) Science , vol.240 , pp. 1198
    • Zein, N.1    Sinha, A.M.2    McGahren, W.J.3    Ellestad, G.A.4
  • 8
    • 0023837723 scopus 로고
    • For previous synthetic work in this area see
    • For previous synthetic work in this area see: P. Magnus and P. A. Carter, J. Am. Chem. Soc., 1988, 110, 1626.
    • (1988) J. Am. Chem. Soc , vol.110 , pp. 1626
    • Magnus, P.1    Carter, P.A.2
  • 20
    • 0016151938 scopus 로고
    • It is interesting to note that diallyl trisulphide and methyl allyl trisulphide are natural products
    • It is interesting to note that diallyl trisulphide and methyl allyl trisulphide are natural products: K. T. Augusti and P. T. Mathew, Experientia, 1974,30,468
    • (1974) Experientia , vol.30 , pp. 468
    • Augusti, K.T.1    Mathew, P.T.2
  • 26
    • 0001595745 scopus 로고
    • The thermal behaviour of dialkyl polysulphides has been studied in connection with vulcanization chemistry
    • The thermal behaviour of dialkyl polysulphides has been studied in connection with vulcanization chemistry. T. L. Pickering, K. J. Saunders, and K. Tobolsky, J. Am. Chem. Soc., 1967, 89, 2364
    • (1967) J. Am. Chem. Soc , vol.89 , pp. 2364
    • Pickering, T.L.1    Saunders, K.J.2    Tobolsky, K.3
  • 27
    • 0002218401 scopus 로고
    • 3Pr
    • B. D. Trivette and A. Y. Coran, J. Org. Chem., 1966, 31, 100. Heating a mixture of EtS3Et and PrS3Pr established an equilbrium containing the latter and EtS3Pr.
    • (1966) J. Org. Chem , vol.31 , pp. 100
    • Trivette, B.D.1    Coran, A.Y.2
  • 31
    • 33845283266 scopus 로고
    • For an extensive study of the thiol-disulphide interchange process
    • For an extensive study of the thiol-disulphide interchange process,: J. Houk and G. M. Whitesides, J. Am. Chem. Soc., 1987, 109, 6825.
    • (1987) J. Am. Chem. Soc , vol.109 , pp. 6825
    • Houk, J.1    Whitesides, G.M.2
  • 32
    • 33947481936 scopus 로고
    • The analysis of the thermolysis and reduction mixture was readily achieved by 1H n.m.r. spectroscopy: (9) δ 4.09 (CH2Ph) and 3.50 (CH2) (12) 3.91 (CH2Ph) and 3.09 (CH2) (22) 4.08 (CH2Ph) (23) 2.55 (CH2Ph) (26) 3.91 (CH2Ph)
    • The analysis of the thermolysis and reduction mixture was readily achieved by 1H n.m.r. spectroscopy: (9) δ 4.09 (CH2Ph) and 3.50 (CH2) (12) 3.91 (CH2Ph) and 3.09 (CH2) (22) 4.08 (CH2Ph) (23) 2.55 (CH2Ph) (26) 3.91 (CH2Ph): D. Grant and J. R. Van Wazer, J. Am.JOURNAL-ISSUE Chem. Soc., 1964, 86, 3012.
    • (1964) J. Am.Journal-Issue Chem. Soc. , vol.86 , pp. 3012
    • Grant, D.1    Van Wazer, J.R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.