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Volumn 32, Issue 5, 2011, Pages 1725-1728

Base-mediated aerobic oxidation of Hagemann's ester: Competitive hydroxylation at C-1 and C-3 positions

Author keywords

Aerobic oxidation; Catechol; Hagemann's ester; Hydroxylation

Indexed keywords


EID: 79957512919     PISSN: 02532964     EISSN: 12295949     Source Type: Journal    
DOI: 10.5012/bkcs.2011.32.5.1725     Document Type: Article
Times cited : (7)

References (31)
  • 1
    • 77950593780 scopus 로고    scopus 로고
    • For the synthesis of Hagemann's ester and related compounds, see, and further references cited therein
    • For the synthesis of Hagemann's ester and related compounds, see: (a) Pollini, G. P.; Benetti, S.; De Risi, C.; Zanirato, V. Tetrahedron 2010, 66, 2775-2802 and further references cited therein.
    • (2010) Tetrahedron , vol.66 , pp. 2775-2802
    • Pollini, G.P.1    Benetti, S.2    De Risi, C.3    Zanirato, V.4
  • 7
    • 0034719949 scopus 로고    scopus 로고
    • For the synthetic applications of Hagemann's ester, see
    • For the synthetic applications of Hagemann's ester, see: (a) Srikrishna, A.; Ramachary, D. B. Tetrahedron Lett. 2000, 41, 2231-2233.
    • (2000) Tetrahedron Lett. , vol.41 , pp. 2231-2233
    • Srikrishna, A.1    Ramachary, D.B.2
  • 24
    • 76949103027 scopus 로고    scopus 로고
    • For recent examples of aerobic oxidation by other groups, see
    • For recent examples of aerobic oxidation by other groups, see: (f) Huang, Y.; Gan, H.; Li, S.; Xu, J.; Wu, X.; Yao, H. Tetrahedron Lett. 2010, 51, 1751-1753.
    • (2010) Tetrahedron Lett. , vol.51 , pp. 1751-1753
    • Huang, Y.1    Gan, H.2    Li, S.3    Xu, J.4    Wu, X.5    Yao, H.6
  • 25
    • 73449145126 scopus 로고    scopus 로고
    • When we repeated the reaction of Stoodley (activated charcoal, EtOAc, reflux, 24 h), C-1-oxidation product was formed as the major one, as reported.3b 6. Trials for obtaining a crystal for X-ray diffraction failed.3a 7. For the synthesis and synthetic applications of 1-substituted Hagemann's ester derivatives, see
    • When we repeated the reaction of Stoodley (activated charcoal, EtOAc, reflux, 24 h), C-1-oxidation product was formed as the major one, as reported.3b 6. Trials for obtaining a crystal for X-ray diffraction failed.3a 7. For the synthesis and synthetic applications of 1-substituted Hagemann's ester derivatives, see: (a) Cui, H.-F.; Yang, Y.-Q.; Chai, Z.; Li, P.; Zheng, C.-W.; Zhu, S.-Z.; Zhao, G. J. Org. Chem. 2010, 75, 117-122.
    • (2010) J. Org. Chem. , vol.75 , pp. 117-122
    • Cui, H.-F.1    Yang, Y.-Q.2    Chai, Z.3    Li, P.4    Zheng, C.-W.5    Zhu, S.-Z.6    Zhao, G.7
  • 29
    • 78549255871 scopus 로고    scopus 로고
    • For NaI/O2-assisted concomitant dealkoxycarbonylation/aerobic oxidation, see
    • For NaI/O2-assisted concomitant dealkoxycarbonylation/aerobic oxidation, see: (a) Lee, H. S.; Kim, S. H.; Kim, Y. M.; Kim, J. N. Tetrahedron Lett. 2010, 51, 5071-5075.
    • (2010) Tetrahedron Lett. , vol.51 , pp. 5071-5075
    • Lee, H.S.1    Kim, S.H.2    Kim, Y.M.3    Kim, J.N.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.