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Volumn 128, Issue 51, 2006, Pages 16482-16483

Catalytic enantioselective hetero-Diels-Alder reactions of an azo compound

Author keywords

[No Author keywords available]

Indexed keywords

AZO COMPOUND;

EID: 33845922379     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja066726y     Document Type: Article
Times cited : (62)

References (46)
  • 1
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    • For a general review of hetero-Diels-Alder reactions, see: a, Fringuelli, F, Taticchi, A, Eds, John Wiley & Sons: New York
    • For a general review of hetero-Diels-Alder reactions, see: (a) The Diels-Alder Reaction: Selected Practical Methods; Fringuelli, F., Taticchi, A., Eds.; John Wiley & Sons: New York, 2002.
    • (2002) The Diels-Alder Reaction: Selected Practical Methods
  • 2
    • 0003497902 scopus 로고    scopus 로고
    • Kobayashi, S, Jørgensen, K. A, Eds, Wiley-VCH: Weinheim, Germany
    • (b) Cycloaddition Reactions in Organic Synthesis; Kobayashi, S., Jørgensen, K. A., Eds.; Wiley-VCH: Weinheim, Germany, 2002; pp 151-209.
    • (2002) Cycloaddition Reactions in Organic Synthesis , pp. 151-209
  • 3
    • 0000085376 scopus 로고    scopus 로고
    • Jacobsen, E. N, Pfaltz, A, Yamamoto, H, Eds, Springer: Berlin
    • (c) Comprehensive Asymmetric Catalysis III; Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer: Berlin, 1999; pp 1237-1254.
    • (1999) Comprehensive Asymmetric Catalysis III , pp. 1237-1254
  • 9
    • 33845927880 scopus 로고    scopus 로고
    • Angew. Chem. 2005, 117, 7244.
    • (2005) Chem , vol.117 , pp. 7244
    • Angew1
  • 12
  • 39
    • 33845931588 scopus 로고    scopus 로고
    • 4 and (R)-BINAP gave the corresponding adduct with >99% ee. The origin of this result is being investigated in our laboratory.
    • 4 and (R)-BINAP gave the corresponding adduct with >99% ee. The origin of this result is being investigated in our laboratory.
  • 40
    • 33845915996 scopus 로고    scopus 로고
    • Reactions using the following metal catalysts were checked on TLC: A1, B, Mg, Zn, Ti, Sc, Hf, Yb, Zr, In, La. None of them accelerated the reaction.
    • Reactions using the following metal catalysts were checked on TLC: A1, B, Mg, Zn, Ti, Sc, Hf, Yb, Zr, In, La. None of them accelerated the reaction.
  • 42
    • 33746654536 scopus 로고    scopus 로고
    • For synthesis of silyloxydienes, see: a
    • For synthesis of silyloxydienes, see: (a) Nakashima, D.; Yamamoto, H. J. Am. Chem. Soc. 2006, 128, 9626.
    • (2006) J. Am. Chem. Soc , vol.128 , pp. 9626
    • Nakashima, D.1    Yamamoto, H.2
  • 44
    • 33845928214 scopus 로고    scopus 로고
    • Excess amount of AcOH was necessary to avoid epimerization of the methyl group via retro-Michael reaction
    • Excess amount of AcOH was necessary to avoid epimerization of the methyl group via retro-Michael reaction.
  • 45
    • 15044355250 scopus 로고    scopus 로고
    • 2-mediated cleavage of the N-N bond with trifluoroacetyl group, see: (a) Chowdari, N. S.; Barbas, C. F., III. Org. Lett. 2005, 7, 867.
    • 2-mediated cleavage of the N-N bond with trifluoroacetyl group, see: (a) Chowdari, N. S.; Barbas, C. F., III. Org. Lett. 2005, 7, 867.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.