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Volumn 73, Issue 5, 2008, Pages 1991-1994

General preparation and controlled cyclization of acyclic terpenoids

Author keywords

[No Author keywords available]

Indexed keywords

ACYCLIC TERPENOIDS; DOUBLE BONDS; ELECTROPHILIC CYCLIZATION;

EID: 41149126166     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo702303a     Document Type: Article
Times cited : (15)

References (30)
  • 2
    • 0003787433 scopus 로고    scopus 로고
    • Barton, D, Nakanishi, K, Eds, Elsevier: Oxford, UK
    • (b) Cane, D. E. In Comprehensive Natural Products Chemistry; Barton, D., Nakanishi, K., Eds.; Elsevier: Oxford, UK, 1999; Vol. 2.
    • (1999) Comprehensive Natural Products Chemistry , vol.2
    • Cane, D.E.1
  • 11
    • 0141653948 scopus 로고    scopus 로고
    • The Friedel-Craft allylation of the prenyl group proceeded efficiently without cyclization in the coenzyme Q-10 synthesis, due to the presence of a benzenesulfonyl group; see: Min, J.-H, Lee, J.-S, Yang, J.-D, Koo, S. J. Org. Chem. 2003, 68, 7925-7927
    • The Friedel-Craft allylation of the prenyl group proceeded efficiently without cyclization in the coenzyme Q-10 synthesis, due to the presence of a benzenesulfonyl group; see: Min, J.-H.; Lee, J.-S.; Yang, J.-D.; Koo, S. J. Org. Chem. 2003, 68, 7925-7927.
  • 26
    • 85026889519 scopus 로고    scopus 로고
    • For another stereoselective chain-extension method for 12a, see: Jin, Y.; Roberts, F. G.; Coates, R. M. Org. Synth. 2007, 84, 43-57.
    • For another stereoselective chain-extension method for 12a, see: Jin, Y.; Roberts, F. G.; Coates, R. M. Org. Synth. 2007, 84, 43-57.
  • 30
    • 41149111697 scopus 로고    scopus 로고
    • The controlled cyclization of compound 13b also worked to give the corresponding monocyclization product in 63% yield, which was 21% lower than that of the cyclization of disulfone 3b, presumably due to instability of the C-S bond under an acidic condition.
    • The controlled cyclization of compound 13b also worked to give the corresponding monocyclization product in 63% yield, which was 21% lower than that of the cyclization of disulfone 3b, presumably due to instability of the C-S bond under an acidic condition.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.