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Volumn 35, Issue 50, 1994, Pages 9403-9406

A highly selective asymmetric methoxyselenylation of alkenes with a chiral ferrocenylselenium reagent

Author keywords

[No Author keywords available]

Indexed keywords

ORGANOSELENIUM DERIVATIVE;

EID: 0028147254     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)78554-6     Document Type: Article
Times cited : (40)

References (8)
  • 3
    • 0002548874 scopus 로고
    • Asymmetric trans-addition reactions of a chiral selenobinaphthyl with prochiral olefins. The case of methoxyselenenylation.
    • (1988) Chemistry Letters , pp. 1895
    • Tomoda1    Iwaoka2
  • 5
    • 0002395879 scopus 로고
    • Asymmetric Oxyselenenylation of Olefins Using Optically Active Selenobinaphthyls and d-Menthol as a Nucleophile.
    • (1992) Chemistry Letters , pp. 1123
    • Fujita1    Iwaoka2    Tomoda3
  • 6
    • 0002375914 scopus 로고
    • Synthesis of Diaryl Diselenides Having Chiral Pyrrolidine Rings with C2 Symmetry. Their Application to the Asymmetric Methoxyselenenylation of trans-.BETA.-Methylstyrenes.
    • (1994) Chemistry Letters , pp. 923
    • Fujita1    Iwaoka2    Tomoda3
  • 8
    • 84912971047 scopus 로고    scopus 로고
    • A slight excess of 1 to bromine was required to obtain a high diastereoselctivity; The use of just an equivalent amount of 1 somewhat decreased the diastereoselectivity (70–80 % de). When excess of bromine was used, the diastereoselectivity extremely diminished (Table 1, entry 3).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.