메뉴 건너뛰기




Volumn , Issue 4, 1999, Pages 664-668

Generation of γ-oxy-substituted benzylithium derivatives by reductive lithiation of 4-phenyl-1,3-dioxanes

Author keywords

Acetals; Carbanions; Electron transfer; Lithiation; Reduction

Indexed keywords

3 PHENYLPROPAN 1 OL DERIVATIVE; ACETAL; ALKALI METAL; ANION; BENZYLLITHIUM DERIVATIVE; DIOXANE DERIVATIVE; LITHIUM DERIVATIVE; NAPHTHALENE; UNCLASSIFIED DRUG;

EID: 0032949502     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1999-3442     Document Type: Article
Times cited : (18)

References (27)
  • 3
    • 0005165550 scopus 로고
    • (a) Bartmann, E. Angew. Chem. 1986, 98, 629; Angew. Chem., Int. Ed. Engl. 1986, 25, 653.
    • (1986) Angew. Chem. , vol.98 , pp. 629
    • Bartmann, E.1
  • 4
    • 84985566360 scopus 로고
    • (a) Bartmann, E. Angew. Chem. 1986, 98, 629; Angew. Chem., Int. Ed. Engl. 1986, 25, 653.
    • (1986) Angew. Chem., Int. Ed. Engl. , vol.25 , pp. 653
  • 11
    • 0001290261 scopus 로고
    • Trost, B. M.; Fleming, I.; Heathcock, C. H., Eds.; Pergamon: Oxford
    • (a) B. B. Snider In Comprehensive Organic Synthesis; Trost, B. M.; Fleming, I.; Heathcock, C. H., Eds.; Pergamon: Oxford, 1991; Vol. 2, p 527.
    • (1991) Comprehensive Organic Synthesis , vol.2 , pp. 527
    • Snider, B.B.1
  • 14
    • 37049104911 scopus 로고
    • (a) Reduction of la with Na/K alloy in DME afforded 2-phenylbutane-1,4-diol (60%), 3-phenylpropan-1-ol (4aa, 23%), as well as minor amounts of dimeric products: Bailey, W. F.; Cioffi, E. A. J. Chem. Soc., Chem. Commun. 1981, 155.
    • (1981) J. Chem. Soc., Chem. Commun. , pp. 155
    • Bailey, W.F.1    Cioffi, E.A.2
  • 15
    • 0345663178 scopus 로고
    • and references cited therein. See also Ref. 12
    • (b) Reduction of la with Na in toluene/butan-1-ol led to the formation of 4aa in 80% yield: Shriner, R. L.; Ruby, P. R. Org. Synth. Coll. Vol. IV, 1963, 798, and references cited therein. See also Ref. 12.
    • (1963) Org. Synth. Coll. , vol.4 , pp. 798
    • Shriner, R.L.1    Ruby, P.R.2
  • 16
    • 85087574584 scopus 로고    scopus 로고
    • note
    • 2O or t-BuOMe as solvents under otherwise identical reaction conditions.
  • 18
    • 0027416797 scopus 로고
    • and references cited therein
    • (a) Diol 6 was prepared by a minor variation of a known procedure: Guijarro, D.; Mancheño, B.; Yus, M. Tetrahedron 1993, 49, 1327, and references cited therein.
    • (1993) Tetrahedron , vol.49 , pp. 1327
    • Guijarro, D.1    Mancheño, B.2    Yus, M.3
  • 23
    • 18944401957 scopus 로고
    • US Patent 2 526 601 (1950)
    • Coes, L. Jr. US Patent 2 526 601 (1950); Chem. Abstr. 1953, 47, 5160h.
    • (1953) Chem. Abstr. , vol.47
    • Coes L., Jr.1
  • 26
    • 0013910921 scopus 로고
    • Pagliarini, G.; Cignarella, G.; Testa, E. Il Farmaco Ed. Sci. 1966, 21, 355; Chem. Abstr. 1966, 65, 7125a.
    • (1966) Chem. Abstr. , vol.65


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.