메뉴 건너뛰기




Volumn , Issue , 1984, Pages 1869-1874

Thermal cycloaddition reactions of thiocarbonyl compounds. Part 1. A novel [4 + 2]cycloaddition reaction of adamantanethione with α,β-unsaturated carbonyl compounds

Author keywords

[No Author keywords available]

Indexed keywords


EID: 37049113114     PISSN: 14704358     EISSN: None     Source Type: Journal    
DOI: 10.1039/P19840001869     Document Type: Article
Times cited : (15)

References (46)
  • 2
    • 0001184378 scopus 로고
    • For reactions as heterodienophiles, see
    • For reactions as heterodienophiles, see (a) S. Weinreb and R. R. Staib, Tetrahedron, 1982, 38, 3087
    • (1982) Tetrahedron , vol.38 , pp. 3087
    • Weinreb, S.1    Staib, R.R.2
  • 3
    • 0003491250 scopus 로고
    • eds. D. H. Barton and W. D. Ollis, Pergamon, Oxford
    • F. Duns, ‘Comprehensive Organic Chemistry,’ eds. D. H. Barton and W. D. Ollis, Pergamon, Oxford, 1978, vol. 3, p. 388
    • (1978) Comprehensive Organic Chemistry , vol.3
    • Duns, F.1
  • 7
    • 0001185415 scopus 로고
    • references cited therein
    • E. Vedejs and D. A. Perry, J. Am. Chem. Soc., 1983, 105, 1683 and references cited therein.
    • (1983) J. Am. Chem. Soc , vol.105 , pp. 1683
    • Vedejs, E.1    Perry, D.A.2
  • 8
    • 0002060470 scopus 로고
    • For use as heterodienes, see
    • For use as heterodienes, see T. Karakasa and S. Motoki, J. Org. Chem., 1978, 43, 4147
    • (1978) J. Org. Chem , vol.43 , pp. 4147
    • Karakasa, T.1    Motoki, S.2
  • 11
    • 0006643260 scopus 로고
    • For use as 1,3-dipolarophiles, see
    • For use as 1,3-dipolarophiles, see R. Huisgen, Angew. Chem., 1963, 75, 605, 742
    • (1963) Angew. Chem , vol.75
    • Huisgen, R.1
  • 15
    • 33947292540 scopus 로고
    • For photocycloadditions, see
    • For photocycloadditions, see P. de Mayo, Acc. Chem. Res., 1971, 4, 41
    • (1971) Acc. Chem. Res , vol.4 , pp. 41
    • de Mayo, P.1
  • 17
    • 84942711300 scopus 로고
    • ed. E. Muller, Houben-Weyl, Stuttgart, Band IV/15b
    • H. Durr, ‘Methoden der Organishen Chemie,’ ed. E. Muller, Houben-Weyl, Stuttgart, 1975, Band IV/15b, Part II, p. 1959.
    • (1975) Methoden der Organishen Chemie
    • Durr, H.1
  • 18
    • 0000293463 scopus 로고
    • For a review on heterodiene synthesis with a,ß-unsaturated carbonyl compounds, see
    • For a review on heterodiene synthesis with a,ß-unsaturated carbonyl compounds, see G. Desimoni and G. Tacconi, Chem. Rev., 1975, 75, 651.
    • (1975) Chem. Rev , vol.75 , pp. 651
    • Desimoni, G.1    Tacconi, G.2
  • 21
    • 84942732088 scopus 로고    scopus 로고
    • 1n various solvents: n-hexane, 498 nm; acetonitrile, 478 nm; 1,4- dioxane 484 nm; chloroform, 484 nm; tetrachloromethane 497 nm; and ethanol, 482 nm, respectively
    • For Diels-Alder reactivity differences in substituted buta-l,3-dienes, ?max. 1n various solvents: n-hexane, 498 nm; acetonitrile, 478 nm; 1,4- dioxane 484 nm; chloroform, 484 nm; tetrachloromethane 497 nm; and ethanol, 482 nm, respectively.
    • For Diels-Alder reactivity differences in substituted buta-l,3-dienes, ?max
  • 39
    • 0001855945 scopus 로고
    • references cited therein
    • R. Huisgen, Acc. Chem. Res., 1977, 10, 117 and references cited therein.
    • (1977) Acc. Chem. Res , vol.10 , pp. 117
    • Huisgen, R.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.