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Volumn , Issue , 1987, Pages 1929-1935

Regioselective Diels-Alder reactions. The nitro group as a regiochemical control element

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EID: 37049076577     PISSN: 14727781     EISSN: None     Source Type: Journal    
DOI: 10.1039/p19870001929     Document Type: Article
Times cited : (36)

References (31)
  • 10
    • 33845379281 scopus 로고
    • intramolecular Diels-Alder reactions of nitroalkenes
    • intramolecular Diels-Alder reactions of nitroalkenes: M. J. Kurth, M. J. O’Brien, H. Hope, and M. Yanock, J. Org. Chem., 1985, 50, 2626.
    • (1985) J. Org. Chem. , vol.50 , pp. 2626
    • Kurth, M.J.1    O’Brien, M.J.2    Hope, H.3    Yanock, M.4
  • 19
    • 0001105970 scopus 로고
    • Rather drastic conditions are required for denitration of secondary nitro groups
    • Rather drastic conditions are required for denitration of secondary nitro groups, N. Ono, H. Miyake, and A. Kaji, J. Org. Chem., 1984, 49, 4997.
    • (1984) J. Org. Chem. , vol.49 , pp. 4997
    • Ono, N.1    Miyake, H.2    Kaji, A.3
  • 20
    • 0001268077 scopus 로고
    • For example, the Diels-Alder reaction of ethylene with butadiene requires temperature of 175 °C and pressure 6 000 p.s.i
    • For example, the Diels-Alder reaction of ethylene with butadiene requires temperature of 175 °C and pressure 6 000 p.s.i., P. D. Bartlett and K. E. Schueller, J. Am. Chem. Soc., 1968, 90, 6071.
    • (1968) J. Am. Chem. Soc. , vol.90 , pp. 6071
    • Bartlett, P.D.1    Schueller, K.E.2
  • 25
    • 0013164330 scopus 로고
    • Similar elimination of methanol to givex,β-unsaturated carbonyl compounds is often reported
    • Similar elimination of methanol to give x,β-unsaturated carbonyl compounds is often reported, T. Shono, H. Nishiguchi, T. Komamura, and M. Sasaki, J. Am. Chem. Soc, 1979,101,984
    • (1979) J. Am. Chem. Soc , vol.101 , pp. 984
    • Shono, T.1    Nishiguchi, H.2    Komamura, T.3    Sasaki, M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.