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Volumn , Issue 6, 2001, Pages 919-923

The first intramolecular Friedel-Crafts reaction of Baylis-Hillman adducts: Synthesis of functionalized indene and indane derivatives

Author keywords

Baylis Hillman reaction; DABCO; Indanes; Indenes; Intramolecular Friedel Crafts reaction; Phosphorus pentoxide

Indexed keywords

DERIVATIVES; HYDROGENATION; SYNTHESIS (CHEMICAL);

EID: 0035039376     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2001-13416     Document Type: Article
Times cited : (48)

References (19)
  • 4
    • 0004106186 scopus 로고
    • McGraw-Hill: New York
    • Smith, M. B. Organic Synthesis; McGraw-Hill: New York, 1994, 1313.
    • (1994) Organic Synthesis , pp. 1313
    • Smith, M.B.1
  • 17
    • 0032552142 scopus 로고    scopus 로고
    • Recently Kim and co-workers have reported the Friedel-Crafts reaction of the Baylis-Hillman adducts of N-tosylimine derivatives with aromatic compounds in the presence of sulfuric acid: Lee, H. J.; Seong, M. R.; Kim, J. N. Tetrahedron Lett. 1998, 39, 6223.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 6223
    • Lee, H.J.1    Seong, M.R.2    Kim, J.N.3
  • 18
    • 85087999734 scopus 로고    scopus 로고
    • note
    • 4 provided the required indene derivative in trace amounts only.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.