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Volumn 120, Issue 30, 1998, Pages 7411-7419

Enantioselective total synthesis of (-)-chlorothricolide via the tandem inter- and intramolecular Diels-Alder reaction of a hexaenoate intermediate

Author keywords

[No Author keywords available]

Indexed keywords

CHLOROTHRICOLIDE;

EID: 0032486756     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja980611f     Document Type: Article
Times cited : (115)

References (101)
  • 4
    • 0016428086 scopus 로고
    • and references therein
    • Schindlet, P. W. Eur. J. Biochem. 1975, 51. 579 and references therein.
    • (1975) Eur. J. Biochem. , vol.51 , pp. 579
    • Schindlet, P.W.1
  • 57
    • 0000048482 scopus 로고
    • Trost, B. M., Ed.; Pergamon Press: Oxford
    • Roush, W. R. In Comprehensive Organic Synthesis: Trost, B. M., Ed.; Pergamon Press: Oxford, 1991; Vol. 5, pp 513-550.
    • (1991) Comprehensive Organic Synthesis , vol.5 , pp. 513-550
    • Roush, W.R.1
  • 80
    • 3543018657 scopus 로고    scopus 로고
    • note
    • Cycloadduct 48 was also obtained as the second most predominant product of the IMDA reaction of 19 performed (125 °C, 24 h, toluene, BHT inhibitor) in the absence of (R)-12. The major product of this reaction, 45. was obtained in 40-47% yield following HPLC purification, while a mixture of 48 and a third IMDA product (presumably corresponding to 47) was obtained in 13-17% yield.
  • 85
    • 3543000625 scopus 로고    scopus 로고
    • note
    • 2.
  • 101
    • 3543022849 scopus 로고    scopus 로고
    • Complete experimental details are provided in the Supporting Information
    • Complete experimental details are provided in the Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.