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Volumn 13, Issue 19, 2011, Pages 5390-5393

Dehydrogenative diels-alder reaction

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Indexed keywords


EID: 80054743505     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol202283d     Document Type: Article
Times cited : (42)

References (41)
  • 2
    • 80054771490 scopus 로고    scopus 로고
    • For related reviews on the Diels-Alder reaction
    • For related reviews on the Diels-Alder reaction
  • 9
    • 80054762280 scopus 로고    scopus 로고
    • For reviews on the synthetic application of the Diels-Alder reaction
    • For reviews on the synthetic application of the Diels-Alder reaction
  • 12
    • 80054748197 scopus 로고    scopus 로고
    • For some recent development of Diels-Alder type reactions
    • For some recent development of Diels-Alder type reactions
  • 21
    • 80054758264 scopus 로고    scopus 로고
    • For reviews on the hetero-Diels-Alder reaction
    • For reviews on the hetero-Diels-Alder reaction
  • 26
    • 80054765121 scopus 로고    scopus 로고
    • For reviews on the retro-Diels-Alder reaction
    • For reviews on the retro-Diels-Alder reaction
  • 32
    • 80054721310 scopus 로고    scopus 로고
    • For reviews on the dehydro-Diels-Alder reaction
    • For reviews on the dehydro-Diels-Alder reaction
  • 37
    • 80054775165 scopus 로고    scopus 로고
    • The reaction of 1a in both the presence and absence of radical initiator azobisisobutyronitrile (5 mol %) under the standard conditions provided cycloadduct 2a in the same yields (78%)
    • The reaction of 1a in both the presence and absence of radical initiator azobisisobutyronitrile (5 mol %) under the standard conditions provided cycloadduct 2a in the same yields (78%).
  • 40
    • 80054737523 scopus 로고    scopus 로고
    • For detailed energy profiles of the reactions and corresponding molecular structures, see Supporting Information
    • For detailed energy profiles of the reactions and corresponding molecular structures, see Supporting Information.
  • 41
    • 80054741933 scopus 로고    scopus 로고
    • The reaction of deuterium-labeled dieneyne 1a produced 2a with 50% deuterium labeling (vide infra). Therefore, the H/D kinetic isotope effect was not observed
    • The reaction of deuterium-labeled dieneyne 1a produced 2a with 50% deuterium labeling (vide infra). Therefore, the H/D kinetic isotope effect was not observed.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.