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Volumn 16, Issue , 1987, Pages 187-238

Stereochemical aspects of the intramolecular Diels-Alder reaction

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EID: 37049076286     PISSN: 03060012     EISSN: None     Source Type: Journal    
DOI: 10.1039/CS9871600187     Document Type: Review
Times cited : (415)

References (173)
  • 12
    • 84943025688 scopus 로고    scopus 로고
    • Ph.D thesis, University of London, 1982. For a review on mechanistic aspects of the Diels-Alder reaction
    • M. P. Edwards, Ph.D thesis, University of London, 1982. For a review on mechanistic aspects of the Diels-Alder reaction.
    • Edwards, M.P.1
  • 15
    • 84943083315 scopus 로고    scopus 로고
    • Products were recovered unchanged after resubjection to thermolysis conditions
    • Products were recovered unchanged after resubjection to thermolysis conditions.
  • 30
    • 0021526965 scopus 로고
    • For a review of the asymmetric Diels-Alder reaction, see, Engl
    • For a review of the asymmetric Diels-Alder reaction, see W. Oppolzer, Angew. Chem., Int. Ed. Engl., 1984, 23, 876.
    • (1984) Angew. Chem., Int. Ed. , vol.23 , pp. 876
    • Oppolzer, W.1
  • 41
    • 0002145249 scopus 로고
    • and references cited therein
    • W. H. Okamura, Act. Chem. Res., 1983, 16, 81 and references cited therein.
    • (1983) Act. Chem. Res. , vol.16 , pp. 81
    • Okamura, W.H.1
  • 78
    • 33947332490 scopus 로고
    • ibid
    • J. B. Hendrickson, ibid., 1967, 89, 7036.
    • (1967) , vol.89 , pp. 7036
    • Hendrickson, J.B.1
  • 97
    • 0008199417 scopus 로고
    • However, a trans.cis ratio of 3:7 has also been claimed for this cyclization
    • K. Shishido, K. Airoya, K. Fukumoto and T. Kametani, Tetrahedron Lett., 1986, 27, 1167. However, a trans.cis ratio of 3:7 has also been claimed for this cyclization.
    • (1986) Tetrahedron Lett. , vol.27 , pp. 1167
    • Shishido, K.1    Airoya, K.2    Fukumoto, K.3    Kametani, T.4
  • 98
    • 0001326527 scopus 로고
    • For a very recent example of high transselectivity resulting from a C-3 diene methyl substituent
    • D. F. Taber, C. Campbell, B. P. Gunn, and I.-C. Chiu, Tetrahedron Lett., 1981, 22, 5141. For a very recent example of high transselectivity resulting from a C-3 diene methyl substituent.
    • (1981) Tetrahedron Lett. , vol.22 , pp. 5141
    • Taber, D.F.1    Campbell, C.2    Gunn, B.P.3    Chiu, I.-C.4
  • 116
    • 0043137897 scopus 로고
    • ibid
    • W. R. Roush and A. G. Myers, ibid., 1981,46, 1509.
    • (1981) , vol.46 , pp. 1509
    • Roush, W.R.1    Myers, A.G.2
  • 134
    • 84987305286 scopus 로고
    • For a related example in which chain substituents caused formation of the d.s-isomer exclusively
    • W. Oppolzer and W. Frostl, Helv. Chim. Acta, 1975, 58, 590. For a related example in which chain substituents caused formation of the d.s-isomer exclusively
    • (1975) Helv. Chim. Acta , vol.58 , pp. 590
    • Oppolzer, W.1    Frostl, W.2
  • 157
    • 0001930760 scopus 로고
    • For a review of the intramolecular imino Diels-Alder reaction, see
    • For a review of the intramolecular imino Diels-Alder reaction, see S. M. Weinreb, Ace. Chem. Res., 1985, 18, 16.
    • (1985) Ace. Chem. Res. , vol.18 , pp. 16
    • Weinreb, S.M.1
  • 166
    • 84943113871 scopus 로고    scopus 로고
    • See reference 13 of reference 103
    • See reference 13 of reference 103.
  • 173
    • 84943118986 scopus 로고    scopus 로고
    • Compare references 65 and 66, for example
    • Compare references 65 and 66, for example.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.