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Volumn 80, Issue 12, 2007, Pages 2443-2445

Novel photoinduced reduction of conjugate dienes by the combination of benzenethiol and diphenyl diselenide

Author keywords

[No Author keywords available]

Indexed keywords

BENZENETHIOL; BINARY SYSTEMS; DIPHENYL DISELENIDE; MILD CONDITIONS; PHOTO INDUCED; XENON LAMPS;

EID: 58149287940     PISSN: 00092673     EISSN: 13480634     Source Type: Journal    
DOI: 10.1246/bcsj.80.2443     Document Type: Article
Times cited : (5)

References (20)
  • 1
    • 0004126864 scopus 로고
    • ed. by R. F. Burk, Springer-Verlag, New York
    • Selenium in Biology and Human Health, ed. by R. F. Burk, Springer-Verlag, New York, 1994.
    • (1994) Selenium in Biology and Human Health
  • 10
    • 14744290401 scopus 로고    scopus 로고
    • ed. by H. Yamamoto, K. Oshima, Wiley-VCH, Weinheim
    • i) A. Ogawa, in Main Group Metals in Organic Synthesis, ed. by H. Yamamoto, K. Oshima, Wiley-VCH, Weinheim, 2004, Vol. 2, p. 813.
    • (2004) Main Group Metals in Organic Synthesis , vol.2 , pp. 813
    • Ogawa, A.1
  • 11
    • 58149290207 scopus 로고    scopus 로고
    • The diene reduction using PhSeH may proceed via (i) the addition of the selenol to diene to form allylic selenide;
    • The diene reduction using PhSeH may proceed via (i) the addition of the selenol to diene to form allylic selenide;
  • 12
    • 58149300208 scopus 로고    scopus 로고
    • the generation of allylic radical from allylic selenide upon photo-irradiation or by the attack of seleno radical;
    • (ii) the generation of allylic radical from allylic selenide upon photo-irradiation or by the attack of seleno radical;
  • 13
    • 0001459562 scopus 로고    scopus 로고
    • -l, see: M. Newcomb, M. B. Manek, J. Am, Chem. Soc. 1990, 112, 9662.
    • -l, see: M. Newcomb, M. B. Manek, J. Am, Chem. Soc. 1990, 112, 9662.
  • 14
    • 33947480236 scopus 로고
    • For the synthesis of 2,3-dimethyl-2-butenyl phenyl sulfide 3a, see for example
    • For the synthesis of 2,3-dimethyl-2-butenyl phenyl sulfide (3a), see for example: A. A. Oswald, K. Griesbaum, W. A. Thaler, B. E. Hudson, Jr., J. Am. Chem. Soc. 1962, 84, 3897.
    • (1962) J. Am. Chem. Soc , vol.84 , pp. 3897
    • Oswald, A.A.1    Griesbaum, K.2    Thaler, W.A.3    Hudson Jr., B.E.4
  • 16
    • 33845183210 scopus 로고    scopus 로고
    • -l. See for example: J. A. Franz, B. A. Bushaw, M. S. Alnajjar, J. Am. Chem. Soc. 1989, 111, 268.
    • -l. See for example: J. A. Franz, B. A. Bushaw, M. S. Alnajjar, J. Am. Chem. Soc. 1989, 111, 268.
  • 17
    • 0001086740 scopus 로고    scopus 로고
    • -1, respectively. See for example: a) G. A. Russell, H. Tashtoush, J. Am. Chem. Soc. 1983, 105, 1398.
    • -1, respectively. See for example: a) G. A. Russell, H. Tashtoush, J. Am. Chem. Soc. 1983, 105, 1398.
  • 20
    • 58149286552 scopus 로고    scopus 로고
    • 2 successfully afforded the thioselenated dienes without the formation of any polymerization products (see: Ref. 2b).
    • 2 successfully afforded the thioselenated dienes without the formation of any polymerization products (see: Ref. 2b).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.