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Volumn 54, Issue 47, 2013, Pages 6298-6302

Inverse electron demand hetero-Diels-Alder reaction in preparing 1,4-benzodioxin from o-quinone and enamine

Author keywords

1,4 Benzodioxins; Diels Alder reaction; Enamines; o Quinones

Indexed keywords

1,4 BENZODIOXIN; ACETAMIDE DERIVATIVE; CLINOPODIC ACID; ENAMINE; IDAZOXAN; IODINE; JUNIPERCOMNOSIDE C; NEOLIGNAN; PHENOL; PHENOL DERIVATIVE; QUINONE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 84885901842     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2013.09.013     Document Type: Article
Times cited : (15)

References (34)
  • 20
    • 84885940890 scopus 로고    scopus 로고
    • (a) Crystallographic data (excluding structure factors) for the structure have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication nos. CCDC 954474. Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK, (fax: +44 (0)1223 336033 or e-mail: deposit@ccdc.cam.ac.Uk). (b)
    • (a) Crystallographic data (excluding structure factors) for the structure have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication nos. CCDC 954474. Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK, (fax: +44 (0)1223 336033 or e-mail: deposit@ccdc.cam.ac.Uk). (b) Sheldrick, G. M. SHELXTL PC, Version 6.12; Bruker Analytical X-ray Systems, Inc.: Madison, WI, 2006.
    • (2006) SHELXTL PC, Version 6.12
    • Sheldrick, G.M.1
  • 24
    • 79957815922 scopus 로고    scopus 로고
    • For recent examples of our work using chemical shift calculations to assist in natural product structure revision and synthetic efforts, see: M.W. Lodewyk, and D.J. Tantillo J. Nat. Prod. 74 2011 1339 1343
    • (2011) J. Nat. Prod. , vol.74 , pp. 1339-1343
    • Lodewyk, M.W.1    Tantillo, D.J.2
  • 29
    • 84885905503 scopus 로고    scopus 로고
    • The CP3 analysis is available through a web-based Java Applet. See http://www-jmg.ch.cam.ac.uk/tools/nmr/.
  • 32
    • 84885920171 scopus 로고
    • Academic Press R. The Conservation of Orbital Symmetry
    • R.B. Woodward Hoffmann 1969 Academic Press R. The Conservation of Orbital Symmetry
    • (1969) Hoffmann
    • Woodward, R.B.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.