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Volumn 44, Issue 2, 2012, Pages 131-145

Tetrahydroisoquinolines by friedel-crafts cyclizations promoted by Iron(III) chloride hexahydrate

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EID: 84859324670     PISSN: 00304948     EISSN: 19455453     Source Type: Journal    
DOI: 10.1080/00304948.2012.643201     Document Type: Article
Times cited : (5)

References (23)
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    • For similar cyclizations using Amberlyst 15 ®, see
    • For similar cyclizations using Amberlyst 15 ®, see J. Young, L. Jung and K. Cheng, Tetrahedron Lett. 41, 3415 (2000).
    • (2000) Tetrahedron Lett. , vol.41 , pp. 3415
    • Young, J.1    Jung, L.2    Cheng, K.3
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    • Chem. Abstr., 146, 462141 (2007).
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    • Chem. Abstr., 142, 430532 (2005).
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    • Precedent does exist for displacement of sulfonamide anions; it was in the context of a threemembered ring opening process, see
    • Precedent does exist for displacement of sulfonamide anions; it was in the context of a threemembered ring opening process, see A. C. Knipe, Tetrahedron Lett., 3031 (1973).
    • (1973) Tetrahedron Lett. , vol.3031
    • Knipe, A.C.1
  • 20
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    • The 1H-NMR spectrum is given in the Supplementary Data.
    • X. Cui, F. Shi, Y. Zhang, and Y. Deng, Tetrahedron Lett., 51, 2048 (2010). The 1H-NMR spectrum is given in the Supplementary Data.
    • (2010) Tetrahedron Lett. , vol.51 , pp. 2048
    • Cui, X.1    Shi, F.2    Zhang, Y.3    Deng, Y.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.