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Volumn 59, Issue 32, 2003, Pages 6039-6044

Intramolecular Diels-Alder reaction leading to tricyclic derivatives as intermediates of natural products synthesis

Author keywords

1,3 allylic strain; Bicyclo 4.3.0 ring derivatives; Intramolecular Diels Alder reaction; Terpenoid

Indexed keywords

3 (4,6 HEPTADIENYL 3 HYDROXY) 2 BUTEN 4 OLIDE; 3 (4,6 HEPTADIENYL 3 TRIISOPROPYLSILYLOXY) 2 BUTEN 4 OLIDE; 3 OXATRICYCLO[7.3.0.0 1,5 ]DODEC 8 ENE 4,10 DIONE; BUTENOLIDE; CHEMICAL COMPOUND; HYDROXYL GROUP; UNCLASSIFIED DRUG;

EID: 0042346411     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(03)01013-5     Document Type: Article
Times cited : (16)

References (29)
  • 7
  • 24
    • 85031143015 scopus 로고    scopus 로고
    • note
    • 2AlCl) were unsuccessful, and further elaboration to optimize the reaction is in progress.
  • 25
    • 85031131729 scopus 로고    scopus 로고
    • note
    • Since 10 and 11 would be converted into the same 4a, a product ratio of the Diels-Alder reaction could be assessed as a sum of 10 and 11 versus 12 ( 10+11:12 =64:36-76:24).
  • 29
    • 85031135970 scopus 로고    scopus 로고
    • note
    • A possibility of electrostatic effect by the polaritic hydroxyl group is also considered.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.