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Volumn 694, Issue 25, 2009, Pages 4100-4106

Synthesis of isoquinolines through the coupling of Fischer carbene complexes with o-alkynylpyridine carbonyl derivatives

Author keywords

Azaisobenzofuran; Diels Alder reaction; Fischer carbene; Heterolignan; Isoquinoline

Indexed keywords

AZAISOBENZOFURAN; DIELS-ALDER REACTION; FISCHER CARBENE; HETEROLIGNAN; ISOQUINOLINE;

EID: 70350090478     PISSN: 0022328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jorganchem.2009.08.019     Document Type: Article
Times cited : (12)

References (58)
  • 14
    • 84944031181 scopus 로고    scopus 로고
    • Isoquinoline Synthesis
    • McKillop A.E., Katrizky A.R., Rees C.W., and Scrivem E.F.V. (Eds), Elsevier, Oxford
    • Balasubramanian M., and Keay J.G. Isoquinoline Synthesis. In: McKillop A.E., Katrizky A.R., Rees C.W., and Scrivem E.F.V. (Eds). In Comprehensive Heterocyclic Chemistry II vol. 5 (1996), Elsevier, Oxford 245-300
    • (1996) In Comprehensive Heterocyclic Chemistry II , vol.5 , pp. 245-300
    • Balasubramanian, M.1    Keay, J.G.2
  • 15
    • 3543059896 scopus 로고    scopus 로고
    • For a review on the synthesis of isoquinoline alkaloid, see:
    • For a review on the synthesis of isoquinoline alkaloid, see:. Chrzanowska M., and Rozwadowska M.D. Chem. Rev. 104 (2004) 3341-3370
    • (2004) Chem. Rev. , vol.104 , pp. 3341-3370
    • Chrzanowska, M.1    Rozwadowska, M.D.2
  • 49
    • 0033015987 scopus 로고    scopus 로고
    • Compound 6 was prepared by the regioselective ortho-lithiation of 3-bromopyridine with LDA at -78 °C followed by quenching with DMF, according to a literature procedure.
    • Compound 6 was prepared by the regioselective ortho-lithiation of 3-bromopyridine with LDA at -78 °C followed by quenching with DMF, according to a literature procedure. Numata A., Kondo Y., and Sakamoto T. Synthesis (1999) 306-311
    • (1999) Synthesis , pp. 306-311
    • Numata, A.1    Kondo, Y.2    Sakamoto, T.3
  • 54
    • 70350128202 scopus 로고    scopus 로고
    • Compound 15 was prepared from carbene complex 2 via deprotonation using n-BuLi at -78 °C followed by addition of an excess allylic bromide according to a literature procedure. Ref. [47].
    • Compound 15 was prepared from carbene complex 2 via deprotonation using n-BuLi at -78 °C followed by addition of an excess allylic bromide according to a literature procedure. Ref. [47].


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.