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Volumn 105, Issue 7, 2005, Pages 2765-2809

Intramolecular dipolar cycloaddition reactions of azomethine ylides

Author keywords

[No Author keywords available]

Indexed keywords

ADDITION REACTIONS; ALDEHYDES; ALKYLATION; AMINES; AMINO ACIDS; ESTERS; FREE RADICAL REACTIONS; ISOMERS; MOLECULAR DYNAMICS; STEREOCHEMISTRY;

EID: 23044431676     PISSN: 00092665     EISSN: None     Source Type: Journal    
DOI: 10.1021/cr040004c     Document Type: Review
Times cited : (1009)

References (203)
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  • 13
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    • Kobayashi, S., Jørgensen, K. A., Eds.; Wiley: New York, Chapter 6
    • Gothelf, K. V. In Cycloaddition Reactions in Organic Synthesis; Kobayashi, S., Jørgensen, K. A., Eds.; Wiley: New York, 2002; Chapter 6, p 211.
    • (2002) Cycloaddition Reactions in Organic Synthesis , pp. 211
    • Gothelf, K.V.1
  • 14
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    • Trost, B. M., Fleming, I., Eds.; Pergamon: Oxford, U.K
    • Wade, P. A. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon: Oxford, U.K., 1991; Vol. 4, p 1111.
    • (1991) Comprehensive Organic Synthesis , vol.4 , pp. 1111
    • Wade, P.A.1
  • 17
    • 0002707988 scopus 로고
    • Curran, D.P., Ed.; Jai Press: Greenwich, C.N
    • Vedejs, E. In Advances in Cycloaddition; Curran, D. P., Ed.; JAI Press: Greenwich, CN, 1988; Vol. 1, p 33.
    • (1988) Advances in Cycloaddition , vol.1 , pp. 33
    • Vedejs, E.1
  • 20
    • 0002430420 scopus 로고
    • Curran, D.P., Ed.; Jai Press: Greenwich, C.N
    • Kanemasa, S.; Tsuge, O. In Advances in Cycloaddition; Curran, D. P., Ed.; JAI Press: Greenwich, CN, 1993; Vol. 3, p 99.
    • (1993) Advances in Cycloaddition , vol.3 , pp. 99
    • Kanemasa, S.1    Tsuge, O.2
  • 21
    • 0001625454 scopus 로고
    • Curran, D.P., Ed.; Jai Press: Greenwich, C.N
    • Grigg, R.; Sridharan, V. In Advances in Cycloaddition; Curran, D. P., Ed.; JAI Press: Greenwich, CN, 1993; Vol. 3, p 161.
    • (1993) Advances in Cycloaddition , vol.3 , pp. 161
    • Grigg, R.1    Sridharan, V.2
  • 30
    • 0002549529 scopus 로고
    • For a historical account of the reaction mechanism, including the debate of stepwise and concerted processes, see
    • For a historical account of the reaction mechanism, including the debate of stepwise and concerted processes, see: Houk, K.N.; González, J.; Li, Y. Acc. Chem. Res. 1995, 28, 81.
    • (1995) Acc. Chem. Res. , vol.28 , pp. 81
    • Houk, K.N.1    González, J.2    Li, Y.3
  • 46
    • 0000048482 scopus 로고
    • Trost, B. M., Fleming, I., Eds.; Pergamon: Oxford, U.K
    • Roush, W. R. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon: Oxford, U.K., 1991; Vol. 5, p 513.
    • (1991) Comprehensive Organic Synthesis , vol.5 , pp. 513
    • Roush, W.R.1
  • 134
    • 23044464468 scopus 로고    scopus 로고
    • note
    • When a solution of the cis-aziridine 290 was irradiated in the presence of the dipolarophile, the trans-pyrrolidine 293 was produced in addition to the expected cis-pyrrolidine 294. The authors ascribed this result to an unknown photoreaction, which competed with the cycloaddition process.
  • 154
    • 0001380727 scopus 로고
    • The absolute stereochemistry of the cycloadduct 366 was confirmed by converting it to the known (2R,3aS,6aS)-octahydrocyclopenta[b]pyrrole-2-carboxylic acid and comparing physical characteristics; see:
    • The absolute stereochemistry of the cycloadduct 366 was confirmed by converting it to the known (2R,3aS,6aS)-octahydrocyclopenta[b]pyrrole -2-carboxylic acid and comparing physical characteristics; see: Urbach, H.; Henning, R. Heterocycles 1989, 28, 957.
    • (1989) Heterocycles , vol.28 , pp. 957
    • Urbach, H.1    Henning, R.2
  • 178
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    • and references therein
    • Berrée, F.; Morel, G. Tetrahedron 1995, 51, 7019 and references therein.
    • (1995) Tetrahedron , vol.51 , pp. 7019
    • Berrée, F.1    Morel, G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.