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Volumn , Issue 17, 2008, Pages 2686-2694

Manganese(III)-mediated direct introduction of 3-oxobutanamides into methoxynaphthalenes

Author keywords

Aromatic substitutions; Cyclizations; Manganese; Oxidations; Radicals

Indexed keywords

AROMATIC SUBSTITUTIONS; CYCLIZATIONS; GOOD YIELDS; MANGANESE(III); MANGANESE-ACETATE; OPTIMIZED REACTION CONDITIONS; OXIDATIONS; RADICALS;

EID: 51949101203     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2008-1067206     Document Type: Article
Times cited : (15)

References (64)
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    • 4143096437 scopus 로고    scopus 로고
    • 1, For reviews, see: a, Oxford University Press: Oxford
    • (1 ) For reviews, see: (a) Zard, S. Z. Radical Reactions in Organic Synthesis; Oxford University Press: Oxford, 2003, 193.
    • (2003) Radical Reactions in Organic Synthesis , pp. 193
    • Zard, S.Z.1
  • 4
    • 51949115925 scopus 로고    scopus 로고
    • Eguchi, S, Ed, Springer: Berlin
    • (b) Nishino, H. In Bioactive Heterocycles I; Eguchi, S., Ed.; Springer: Berlin, 2006, 39.
    • (2006) Bioactive Heterocycles I , pp. 39
    • Nishino, H.1
  • 43
    • 51949087263 scopus 로고
    • Eur. Pat. Appl. EP 316097, 232794
    • (h) Edwards, P. N.; Large, M. S. Eur. Pat. Appl. EP 316097, 1989; Chem. Abstr. 1989, 111, 232794.
    • (1989) Chem. Abstr , vol.111
    • Edwards, P.N.1    Large, M.S.2
  • 58
    • 51949096051 scopus 로고    scopus 로고
    • The total yield of the products 3aa, 4aa, and 5aa was 48% (entry 1), 54% (entry 2), and 57% yield (entry 3), respectively.
    • The total yield of the products 3aa, 4aa, and 5aa was 48% (entry 1), 54% (entry 2), and 57% yield (entry 3), respectively.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.