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Volumn 15, Issue 19, 2013, Pages 4952-4955

Synthetic studies toward the citrinadin A and B core architecture

Author keywords

[No Author keywords available]

Indexed keywords

CITRINADIN A; INDOLE ALKALOID; PYRIDINE DERIVATIVE;

EID: 84885120101     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol402177a     Document Type: Article
Times cited : (17)

References (24)
  • 16
    • 84885088133 scopus 로고    scopus 로고
    • The Wood group has also demonstrated this epoxide opening on C-7 substituted derivatives of 15. See: Progress toward the Total Synthesis of the Citrinadins, Ph.D. Thesis, Colorado State University, Fort Collins, CO.
    • The Wood group has also demonstrated this epoxide opening on C-7 substituted derivatives of 15. See: Smith, G. M. Progress toward the Total Synthesis of the Citrinadins, Ph.D. Thesis, Colorado State University, Fort Collins, CO, 2012.
    • (2012)
    • Smith, G.M.1
  • 17
    • 84864609130 scopus 로고    scopus 로고
    • The work of Wonjacynska et al. has shown that aziridinium openings may proceed with retention of stereochemistry, which supports the possible intermediacy of 16: Wojaczynska, E.; Turowska-Tryk, I.; Skarzewski, J. Tetrahedron 2012, 68, 7848-7854
    • (2012) Tetrahedron , vol.68 , pp. 7848-7854
    • Wojaczynska, E.1    Turowska-Tryk, I.2    Skarzewski, J.3
  • 18


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.