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Volumn 2, Issue 2, 2005, Pages 147-155

Utilization of phenyl trialkylstannyl selenide as a promising reagent for introduction of the phenylseleno group

Author keywords

Acetal; Aroyl halide; Aryl halide; Carbon monoxide; Epoxide; Lewis acid; Organoselenium compound; Palladium catalyst; Phenyl tributylstannyl selenide; bromo ketone

Indexed keywords

CATALYSTS; KETONES; PALLADIUM COMPOUNDS; SELENIUM COMPOUNDS;

EID: 33646039392     PISSN: 1570193X     EISSN: None     Source Type: Journal    
DOI: 10.2174/1570193053544463     Document Type: Review
Times cited : (9)

References (30)
  • 3
    • 0002045618 scopus 로고
    • Trost, B. M, Ed. Pergamon Press; Oxford
    • a) Kricf. A. In Comprehensive Organic Synthesis; Trost, B. M., Ed. Pergamon Press; Oxford, 1991; Vol. 3, pp. 85-192
    • (1991) Comprehensive Organic Synthesis , vol.3 , pp. 85-192
    • Kricf, A.1
  • 6
    • 85189271477 scopus 로고    scopus 로고
    • Patai, S.; Rappoport, Z. In The Chemistry of Organic Selenium and Tellurium Compounds; Wiley: New York, 1986; Vols. I and 2
    • d) Patai, S.; Rappoport, Z. In The Chemistry of Organic Selenium and Tellurium Compounds; Wiley: New York, 1986; Vols. I and 2
  • 7
    • 85189267847 scopus 로고    scopus 로고
    • 0 = 98.2 + 3 kcal/mol. See: Ho. K. C. M. In Thermodynamic Data for Inoganic Sulfides, Selenides, and Tellurides; Rechhood Press: England, 1974; p 594.
    • 0 = 98.2 + 3 kcal/mol. See: Ho. K. C. M. In Thermodynamic Data for Inoganic Sulfides, Selenides, and Tellurides; Rechhood Press: England, 1974; p 594.
  • 8
    • 85189261718 scopus 로고    scopus 로고
    • The other application of organoselenium compounds having a Se-Sn bond are very few 6-12.
    • The other application of organoselenium compounds having a Se-Sn bond are very few 6-12.
  • 16
    • 0004171901 scopus 로고
    • Beletskaya's group has also reported the utilization of phenyl tributylstannyl selenide, which was generated in situ by the reaction of diphenyl diselenide with hexabutyl ditannnane under the irradiation of daylight in organic synthesis. See: a
    • Beletskaya's group has also reported the utilization of phenyl tributylstannyl selenide, which was generated in situ by the reaction of diphenyl diselenide with hexabutyl ditannnane under the irradiation of daylight in organic synthesis. See: a) Bumagin, N. A.; Gulevich, Y. V.; Beletskaya, I. P. Izu. Akad. Nauk SSSR, Ser. Khim. 1984, 953.
    • (1984) Izu. Akad. Nauk SSSR, Ser. Khim , pp. 953
    • Bumagin, N.A.1    Gulevich, Y.V.2    Beletskaya, I.P.3
  • 21
    • 85189253179 scopus 로고    scopus 로고
    • 2 in 83 % isolated yield. See: Han, L. -B.; Shimada, S.; Tanaka, M. J. Am. Chem. Soc. 1997, 119, 8133.
    • 2 in 83 % isolated yield. See: Han, L. -B.; Shimada, S.; Tanaka, M. J. Am. Chem. Soc. 1997, 119, 8133.
  • 24
    • 0001729405 scopus 로고
    • For recent reviews on selenol esters: a, Trost, B. M, Fleming, I, Eds; Pergamon: Oxford
    • For recent reviews on selenol esters: (a) Ogawa, A.; Sonoda, N. In Comprehensive Organic Synthesis; Trost, B. M.; Fleming, I., Eds; Pergamon: Oxford, 1991; Vol. 6. pp. 461-484.
    • (1991) Comprehensive Organic Synthesis , vol.6 , pp. 461-484
    • Ogawa, A.1    Sonoda, N.2
  • 26
    • 85189273007 scopus 로고    scopus 로고
    • Palladium-catalyzed carbonylation has been extensively investigated and widely used in organic synthesis. See: a Schoenberg, A, Bartolettic, I, Heck, R. F. J. Org. Chem. 1974, 39, 3318
    • Palladium-catalyzed carbonylation has been extensively investigated and widely used in organic synthesis. See: a) Schoenberg, A.; Bartolettic, I.; Heck, R. F. J. Org. Chem. 1974, 39, 3318.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.