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Volumn 12, Issue 20, 2010, Pages 4560-4563

Erratum: Synthesis of the tetracyclic core of tetrapetalone A enabled by a pyrrole reductive alkyation (Organic Letters (2010) 12:20 (4560) DOI:10.1021/ol1018536);Synthesis of the tetracyclic core of tetrapetalone a enabled by a pyrrole reductive alkyation

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EID: 77957824344     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol501550u     Document Type: Erratum
Times cited : (56)

References (41)
  • 5
    • 77957851240 scopus 로고    scopus 로고
    • For a discussion, see ref 1b.
    • For a discussion, see ref 1b.
  • 7
    • 77957838644 scopus 로고    scopus 로고
    • Porco's earlier report of an advanced tetracyclic intermediate has been retracted, see
    • Porco's earlier report of an advanced tetracyclic intermediate has been retracted, see
  • 11
    • 77957827778 scopus 로고    scopus 로고
    • For selected examples, see
    • For selected examples, see
  • 21
    • 77957845803 scopus 로고    scopus 로고
    • Several conditions including those popularized by Buchwald and Hartwig were attempted, see
    • Several conditions including those popularized by Buchwald and Hartwig were attempted, see
  • 28
    • 77957853933 scopus 로고    scopus 로고
    • For details, see the Supporting Information.
    • For details, see the Supporting Information.
  • 31
    • 77957855358 scopus 로고    scopus 로고
    • 3 inhibits this oxidation reaction, suggesting the importance of acid for the transformation.
    • 3 inhibits this oxidation reaction, suggesting the importance of acid for the transformation.
  • 37
    • 77957830107 scopus 로고    scopus 로고
    • Deprotonation alpha to the ketone group is presumably not favorable because of poor orbital overlap of the C - H bond and the π* of the C=O bond.
    • Deprotonation alpha to the ketone group is presumably not favorable because of poor orbital overlap of the C - H bond and the π* of the C=O bond.
  • 39
    • 77957856916 scopus 로고    scopus 로고
    • Modification of the original conditions included addition of a CuCl.
    • Modification of the original conditions included addition of a CuCl.
  • 41
    • 77957852921 scopus 로고    scopus 로고
    • Prolonged exposure of 20 to Dess - Martin periodinane resulted in the formation of 24, which is closely related to the tetracyclic core of tetrapetalones C and D.
    • Prolonged exposure of 20 to Dess - Martin periodinane resulted in the formation of 24, which is closely related to the tetracyclic core of tetrapetalones C and D.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.