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Volumn 47, Issue 5, 2008, Pages 910-912

One-step synthesis and exploratory chemistry of [5]dendralene

Author keywords

Dendralene; Diels Alder reactions; Domino reactions; Electrocyclic reactions; Hydrocarbons

Indexed keywords

DIELS-ALDER REACTIONS; ELECTROCYCLIC REACTIONS;

EID: 38549176201     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200704470     Document Type: Article
Times cited : (44)

References (26)
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    • 2].
    • 2].
  • 15
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    • The crude product is contaminated with up to 10% [4]dendralene, which is the result of an oxidative dimerization process. This more volatile contaminant is easily removed by vacuum distillation.
    • The crude product is contaminated with up to 10% [4]dendralene, which is the result of an oxidative dimerization process. This more volatile contaminant is easily removed by vacuum distillation.
  • 16
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    • For a review of diene-transmissive Diels-Alder reactions, see
    • For a review of diene-transmissive Diels-Alder reactions, see: J. D. Winkler, Chem. Rev. 1996, 96, 167-176.
    • (1996) Chem. Rev , vol.96 , pp. 167-176
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    • All cycloadditions involving maleimide dienophiles were found to proceed exclusively through the endo mode.
    • All cycloadditions involving maleimide dienophiles were found to proceed exclusively through the endo mode.
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    • -1 is one-half that measured for the other three compounds.
    • -1 is one-half that measured for the other three compounds.
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    • See the Supporting Information for crystallographic details
    • See the Supporting Information for crystallographic details.
  • 23
    • 38549132802 scopus 로고    scopus 로고
    • The diene site selectivity witnessed during this cycloaddition is identical to that seen in the reaction of 1 with NMM (Scheme 3).
    • The diene site selectivity witnessed during this cycloaddition is identical to that seen in the reaction of 1 with NMM (Scheme 3).
  • 24
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    • a) R. Keese, Chem. Rev. 2006, 106, 4787-4808;
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.