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Volumn 44, Issue 1, 2003, Pages 119-122

Installation of carbon chain onto 2-cyclohexene-1,4-diol monoacetate

Author keywords

Copper catalyst; Coupling reaction; Cyclohexene 1,4 diol monoacetate; Grignard reagent; Lithium borates; Nickel catalyst

Indexed keywords

2 CYCLOHEXENE 1,4 DIOL MONOACETATE; ACETIC ACID DERIVATIVE; BORIC ACID; CARBON; COPPER DERIVATIVE; NICKEL; UNCLASSIFIED DRUG;

EID: 0037213616     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(02)02494-2     Document Type: Article
Times cited : (3)

References (30)
  • 9
    • 0012019271 scopus 로고    scopus 로고
    • 2 and RCu(CN)(MgX) are used to indicate the 10∼15:1, 2:1, and 1:1 ratios of RMgX/CuCN, respectively, though the precise structures of the latter two reagents are not elucidated.
    • 2 and RCu(CN)(MgX) are used to indicate the 10∼15:1, 2:1, and 1:1 ratios of RMgX/CuCN, respectively, though the precise structures of the latter two reagents are not elucidated.
  • 25
    • 37049072971 scopus 로고
    • Alkylation of (SAMP)- or (RAMP)-hydrazone i might be an alternative way to compounds such as 8 and 9. To the best of our knowledge, however, alkylation of hydrazone i takes place at the α′-position instead of the α- or γ-position: (a) Iio, H.; Monden, M.; Okada, K.; Tokoroyama, T. J. Chem. Soc., Chem. Commun. 1987, 358-359; (b) Enders, D.; Eichenauer, H. Chem. Ber. 1979, 112, 2933-2960. Such ketones in optically active forms are accessible by the present method (Eqs. (2) and (3)) using optically active cyclohexene 1.
    • (1987) J. Chem. Soc., Chem. Commun. , pp. 358-359
    • Iio, H.1    Monden, M.2    Okada, K.3    Tokoroyama, T.4
  • 26
    • 84982456512 scopus 로고
    • Such ketones in optically active forms are accessible by the present method (Eqs. (2) and (3)) using optically active cyclohexene 1.
    • Alkylation of (SAMP)- or (RAMP)-hydrazone i might be an alternative way to compounds such as 8 and 9. To the best of our knowledge, however, alkylation of hydrazone i takes place at the α′-position instead of the α- or γ-position: (a) Iio, H.; Monden, M.; Okada, K.; Tokoroyama, T. J. Chem. Soc., Chem. Commun. 1987, 358-359; (b) Enders, D.; Eichenauer, H. Chem. Ber. 1979, 112, 2933-2960. Such ketones in optically active forms are accessible by the present method (Eqs. (2) and (3)) using optically active cyclohexene 1.
    • (1979) Chem. Ber. , vol.112 , pp. 2933-2960
    • Enders, D.1    Eichenauer, H.2
  • 28
    • 0012080927 scopus 로고    scopus 로고
    • note
    • 4Cl. The mixture was extracted with EtOAc and the crude product was purified by chromatography on silica gel to afford the products shown in Table 2.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.