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Volumn , Issue 13, 2006, Pages 2035-2038

A single-step synthesis of symmetrical 1,3-diarylisobenzofurans

Author keywords

Diels Alder reactions; Fused ring systems; Grignard reactions; Heterocycles; Nucleophilic addition

Indexed keywords

1,3 DIARYLISOBENZOFURAN DERIVATIVE; 3 METHOXY 3H ISOBENZOFURAN 1 ONE; 3 METHOXYPHTHALIDE; ALDEHYDE DERIVATIVE; BENZOFURAN DERIVATIVE; ISOBENZOFURAN DERIVATIVE; PHTHALALDEHYDIC ACID; PHTHALIDE DERIVATIVE; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE; POLYMETHOXYLATED ISOBENZOFURAN; UNCLASSIFIED DRUG;

EID: 33748270858     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-948179     Document Type: Article
Times cited : (18)

References (22)
  • 3
    • 24944468882 scopus 로고    scopus 로고
    • Thomas, E. J., Ed.; Thieme: Stuttgart
    • (c) Steel, P. G. Science of Synthesis, Vol. 10; Thomas, E. J., Ed.; Thieme: Stuttgart, 2001, 87.
    • (2001) Science of Synthesis , vol.10 , pp. 87
    • Steel, P.G.1
  • 4
    • 0023952038 scopus 로고
    • For a review, see: Rodrigo, R. Tetrahedron 1988, 44, 2093.
    • (1988) Tetrahedron , vol.44 , pp. 2093
    • Rodrigo, R.1
  • 21
    • 33748277257 scopus 로고    scopus 로고
    • note
    • An alternative pathway could be nucleophilic addition of 3a to the carbonyl group of 1a as the first step. This seems unlikely, as the sole isolated compound resulting from reaction of 1a with only one equiv of 3a was phthalide 4a.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.