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Volumn 65, Issue 14, 2000, Pages 4309-4314

PhSeSiR3-catalyzed group transfer radical reactions

Author keywords

[No Author keywords available]

Indexed keywords

ASCORBIC ACID; PHENYL GROUP; SELENIUM;

EID: 0034647518     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo000128z     Document Type: Article
Times cited : (18)

References (76)
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    • note
    • (b) For leading references, see: reference 40a and the references therein.
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    • note
    • For leading references, see: reference 2 and the references therein.
  • 18
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    • (a) Amato, J. Science 1993, 259, 1538.
    • (1993) Science , vol.259 , pp. 1538
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  • 19
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    • (b) Illman, D. L. Chem. Eng. News 1993, 71 (13), 5; 1994, 72 (36), 22.
    • (1993) Chem. Eng. News , vol.71 , Issue.13 , pp. 5
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    • (b) Illman, D. L. Chem. Eng. News 1993, 71 (13), 5; 1994, 72 (36), 22.
    • (1994) Chem. Eng. News , vol.72 , Issue.36 , pp. 22
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    • Ph.D. Thesis, submitted to University of Pune
    • Rao, K. S. S. P., Ph.D. Thesis, submitted to University of Pune, 1998.
    • (1998)
    • Rao, K.S.S.P.1
  • 42
    • 23244464458 scopus 로고
    • John Wiley & Sons: New York
    • - to PhSeSePh is not known, it is understood to be much higher than the oxidative dimerization of PhSeH. Encyclopaedia of Reagents in Organic Synthesis; Paquette, L. A., Ed.; John Wiley & Sons: New York, 1995; Vol. 1, p 270.
    • (1995) Encyclopaedia of Reagents in Organic Synthesis , vol.1 , pp. 270
    • Paquette, L.A.1
  • 52
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    • whereas compound 17 was prepared by the nucleophilic displacement of phenylselenyl anion on the corresponding bromide
    • (a) For the preparation of compound 15 and 16, see: Engman, L.; Gupta, V. J. Org. Chem. 1997, 62, 157 whereas compound 17 was prepared by the nucleophilic displacement of phenylselenyl anion on the corresponding bromide (cf: Sharpless, K. B. J. Am. Chem. Soc. 1973, 95, 2697).
    • (1997) J. Org. Chem. , vol.62 , pp. 157
    • Engman, L.1    Gupta, V.2
  • 53
    • 0007590568 scopus 로고
    • (a) For the preparation of compound 15 and 16, see: Engman, L.; Gupta, V. J. Org. Chem. 1997, 62, 157 whereas compound 17 was prepared by the nucleophilic displacement of phenylselenyl anion on the corresponding bromide (cf: Sharpless, K. B. J. Am. Chem. Soc. 1973, 95, 2697).
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 2697
    • Sharpless, K.B.1
  • 56
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    • Trost, B. M., Flemming, I., Eds.; Pergamon: Oxford
    • (b) Curran, D. P. In Comprehensive Organic Synthesis; Trost, B. M., Flemming, I., Eds.; Pergamon: Oxford, 1991; Vol. 4, p 715.
    • (1991) Comprehensive Organic Synthesis , vol.4 , pp. 715
    • Curran, D.P.1
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    • note
    • (c) Also see: reference 37c.
  • 71
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    • Van Nostrand Reinhold Company: New York
    • This strategy could be considered ecologically compatible as in this approach the only molecule which undergoes chemical destruction is the ascorbic acid. No selenium-containing compound is produced as byproduct. Moreover, organoselenium compounds are known to be less toxic than their inorganic counterparts. Aromatic selenium compounds seems to be still less toxic than aliphatic selenium compounds. For detailed toxicological data on selenium compounds see: In Selenium; Zingaro, R. A., Cooper, C. W., Ed.; Van Nostrand Reinhold Company: New York, 1974; p 669.
    • (1974) Selenium , pp. 669
    • Zingaro, R.A.1    Cooper, C.W.2
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    • note
    • (b) Also see references 21 and 22.
  • 76
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    • note
    • (b) For a modified synthesis, see: reference 14b.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.