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Volumn 48, Issue 1, 2009, Pages 179-182

Synthesis of 3,4-dihydroisoquinolines by a C(sp3)-H activation/electrocyclization strategy: Total synthesis of coralydine

Author keywords

Alkaloids; C H activation; Electrocyclic reactions; Heterocycles; Natural products

Indexed keywords

ACTIVATION ANALYSIS; ALKALOIDS; CHEMICAL ACTIVATION; METABOLITES;

EID: 58249124539     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200804444     Document Type: Article
Times cited : (108)

References (40)
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    • For examples of electrocyclizations from BCB, see ref, 2a] and: a T. Kametani, K. Ogasawara, T. Takahashi, J. Chem. Soc. Chem. Commun. 1972, 675-676;
    • For examples of electrocyclizations from BCB, see ref. [2a] and: a) T. Kametani, K. Ogasawara, T. Takahashi, J. Chem. Soc. Chem. Commun. 1972, 675-676;
  • 25
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    • With aliphatic aldehydes, the isolated product was that depicted below, rather than the desired DHIQ: It presumably arose from outward rotation of the imine, followed by tandem [1,5]-hydrogen shifts [Eq 1, Chemical Equation Presented
    • With aliphatic aldehydes, the isolated product was that depicted below, rather than the desired DHIQ: It presumably arose from outward rotation of the imine, followed by tandem [1,5]-hydrogen shifts [Eq (1)]. (Chemical Equation Presented)
  • 37
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    • L. C. Gobbi, T. Luebbers, P. Mattei, R. Narquizian, P. C. Wyss (Hoffmann-La Roche AG), WO03055881, 2003.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.