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Volumn 3, Issue 9, 2012, Pages 2849-2852

A chemical synthesis of 11-methoxy mitragynine pseudoindoxyl featuring the interrupted Ugi reaction

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL SYNTHESIS; DIASTEREOSELECTIVE; ELECTRON-RICH AROMATICS; FUNCTIONALIZED; NEW MEMBERS; PIPERIDINE RINGS; REDUCTIVE CYCLIZATION; UGI REACTION;

EID: 84864480742     PISSN: 20416520     EISSN: 20416539     Source Type: Journal    
DOI: 10.1039/c2sc20669b     Document Type: Article
Times cited : (47)

References (33)
  • 9
    • 0033790476 scopus 로고    scopus 로고
    • The oxidative rearrangement was achieved in three steps with an overall yield of 21%
    • H. Takayama N. Aimi S.-i. Sakai Yakugaku Zasshi 2000 120 10 959 967
    • (2000) Yakugaku Zasshi , vol.120 , Issue.10 , pp. 959-967
    • Takayama, H.1    Aimi, N.2    Sakai, S.I.3
  • 19
    • 84864464756 scopus 로고    scopus 로고
    • This manuscript is based on the PhD thesis of Jimin Kim, Princeton University
    • This manuscript is based on the PhD thesis of Jimin Kim, Princeton University, September 2010
    • (2010)
  • 23
    • 0025865144 scopus 로고
    • Efforts to annulate the spiro-fused indoxyl system onto advanced, piperidine-containing intermediates were frustrated by low yields. Discussions are found in ref. 9
    • H. Takahata Y. Banba T. Momose Tetrahedron: Asymmetry 1991 2 445 448
    • (1991) Tetrahedron: Asymmetry , vol.2 , pp. 445-448
    • Takahata, H.1    Banba, Y.2    Momose, T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.