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Volumn 4, Issue 24, 2006, Pages 4409-4430

From α-cedrene to crinipellin B and onward: 25 years of the alkene-arene meta-photocycloaddition reaction in natural product synthesis

Author keywords

[No Author keywords available]

Indexed keywords

ADDITION REACTIONS; AROMATIZATION; PHOTOCHEMICAL REACTIONS; SYNTHESIS (CHEMICAL);

EID: 33751576585     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b614011b     Document Type: Article
Times cited : (60)

References (112)
  • 7
    • 0004167906 scopus 로고
    • W. M. Hoorspool, Plenum Press, New York, pp. 1-60, ISBN 0-306-41449-X
    • A. Gilbert, in Synthetic Organic Photochemistry, ed., W. M. Hoorspool, Plenum Press, New York, 1984, pp. 1-60, ISBN 0-306-41449-X
    • (1984) Synthetic Organic Photochemistry, Ed.
    • Gilbert In, A.1
  • 8
    • 33751583545 scopus 로고    scopus 로고
    • W. M. Hoorspool and F. Lenci, CRC Press Inc., Boca Raton, ch. 41, pp. 41/1-41/11, ISBN 0-8493-1348-1
    • A. Gilbert, in CRC Handbook of Organic Photochemistry and Photobiology, ed., W. M. Hoorspool, and, F. Lenci, CRC Press Inc., Boca Raton, 2004, ch. 41, pp. 41/1-41/11, ISBN 0-8493-1348-1
    • (2004) CRC Handbook of Organic Photochemistry and Photobiology, Ed.
    • Gilbert In, A.1
  • 13
    • 0001485998 scopus 로고
    • Allenes, though not always giving high yielding reactions, frequently favour para-addition:
    • D. De Keukeleire S.-L. He Chem. Rev. 1993 93 359 380
    • (1993) Chem. Rev. , vol.93 , pp. 359-380
    • De Keukeleire, D.1    He, S.-L.2
  • 25
    • 0010635437 scopus 로고
    • A very interesting case, in which a strong p-donor group did not dictate the regiochemistry of a cycloaddition, was reported by Gilbert and Blakemore:
    • A. Gilbert P. Yianni Tetrahedron 1981 37 3275 3283
    • (1981) Tetrahedron , vol.37 , pp. 3275-3283
    • Gilbert, A.1    Yianni, P.2
  • 36
    • 84903506013 scopus 로고
    • Aromatic Compounds: Isomerism and Cycloaddition, in
    • J. D. Coyle, Royal Society of Chemistry, London, UK, ch. 12, pp. 226-255, ISBN 0-85186-656-5
    • P. A. Wender and T. W. von Geldern, Aromatic Compounds: Isomerism and Cycloaddition, in Photochemistry in Organic Synthesis, ed., J. D. Coyle, Royal Society of Chemistry, London, UK, 1986, ch. 12, pp. 226-255, ISBN 0-85186-656-5
    • (1986) Photochemistry in Organic Synthesis, Ed.
    • Wender, P.A.1    Von Geldern, T.W.2
  • 44
  • 61
    • 33751569608 scopus 로고
    • J. D. Coyle, Royal Society of Chemistry, London, UK, ch. 2, pp. 19-38, ISBN 0-85186-656-5 By virtue of the facile rearrangement of the tertiary allylic bromide only 10β-bromocedrene-11-one resulted from the first step For an alternative [5 + 2] cycloaddition approach to pipitzol see:
    • A 2 mm Vycor filter sees an increase in transmittance from 10-80% on going from 210-240 nm wavelength light: J. Hutchinson, in Photochemistry in Organic Synthesis, ed., J. D. Coyle, Royal Society of Chemistry, London, UK, 1986, ch. 2, pp. 19-38, ISBN 0-85186-656-5
    • (1986) Photochemistry in Organic Synthesis, Ed.
    • Hutchinson In, J.1
  • 85
    • 0344815173 scopus 로고
    • Chanon defines this as: "Holosynthon: a structural entity specifically designed to make possible a great change in complexity or similarity (between this structural entity and its successor) when a one-pot reaction or set of reactions is applied to it." Ref. 16
    • T. Ohsawa T. Kobayashi Y. Mizuguchi T. Saitoh T. Oishi Tetrahedron Lett. 1985 26 6103 6106
    • (1985) Tetrahedron Lett. , vol.26 , pp. 6103-6106
    • Ohsawa, T.1    Kobayashi, T.2    Mizuguchi, Y.3    Saitoh, T.4    Oishi, T.5
  • 90
    • 33751565849 scopus 로고
    • National Organic Chemistry Symposium in Minneapolis
    • G. Stork, 1991, National Organic Chemistry Symposium in Minneapolis
    • (1991)
    • Stork, G.1
  • 91


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.