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Volumn 39, Issue 12, 2000, Pages 2152-2155

A highly efficient triplet analogue of a thermal biradical cyclization - The photochemical C2-C6 cyclization of enyne-heteroallenes

Author keywords

Diradicals; Heterocumulenes; Nitrogen heterocycles; Photocyclizations; Sensitizers

Indexed keywords

ALLENE DERIVATIVE;

EID: 0039592895     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/1521-3773(20000616)39:12<2152::AID-ANIE2152>3.0.CO;2-4     Document Type: Article
Times cited : (76)

References (49)
  • 5
    • 0000770422 scopus 로고    scopus 로고
    • Reviews: a) K. K. Wang, Chem. Rev. 1996, 96, 207-222;
    • (1996) Chem. Rev. , vol.96 , pp. 207-222
    • Wang, K.K.1
  • 11
    • 0030515269 scopus 로고    scopus 로고
    • c) M. Schmittel, M. Strittmatter, S. Kiau, Angew. Chem. 1996, 108, 1952-1954; Angew. Chem. Int. Ed. Engl. 1996, 35, 1843-1845;
    • (1996) Angew. Chem. Int. Ed. Engl. , vol.35 , pp. 1843-1845
  • 14
    • 0032479752 scopus 로고    scopus 로고
    • e) B. Engels, C. Lennartz, M. Hanrath, M. Schmittel, M. Strittmatter, Angew. Chem. 1998, 110, 2067-2070; Angew. Chem. Int. Ed. 1998, 37, 1960-1963.
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 1960-1963
  • 16
    • 0032546774 scopus 로고    scopus 로고
    • a) M. Schmittel, J.-P. Steffen, M. Á. Wencesla Ángel, B. Engels, C. Lennartz, M. Hanrath, Angew. Chem. 1998, 110, 1633-1635; Angew. Chem. Int. Ed. 1998, 37, 1562-1564;
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 1562-1564
  • 18
    • 0032544307 scopus 로고    scopus 로고
    • b) M. Schmittel, J.-P. Steffen, B. Engels, C. Lennartz, M. Hanrath, Angew. Chem. 1998, 110, 2531-2533; Angew. Chem. Int. Ed. 1998, 37, 2371-2373.
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 2371-2373
  • 32
    • 0033519293 scopus 로고    scopus 로고
    • c) T. Kaneko, M. Takahashi, M. Hirama, Angew. Chem. 1999, 111, 1347-1349; Angew. Chem. Int. Ed. 1999, 38, 1267-1268.
    • (1999) Angew. Chem. Int. Ed. , vol.38 , pp. 1267-1268
  • 44
    • 0343331102 scopus 로고    scopus 로고
    • note
    • Calculations on a higher level of theory have commenced in cooperation with B. Engels (Würzburg, Germany).
  • 46
    • 0343766941 scopus 로고    scopus 로고
    • note
    • Product 5 is formed through the loss of a methyl group from the intermediate, a formally Diels - Alder product. According to preliminary studies, this is also a photochemical process which will be detailed in the full paper to come.
  • 49
    • 0031801543 scopus 로고    scopus 로고
    • b) R. Marquardt, A. Balster, W. Sander, E. Kraka, D. Cremer, J. G. Radziszewski, Angew. Chem. 1998, 110, 1001-1005; Angew. Chem. Int. Ed. 1998, 37, 955-958.
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 955-958


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.