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Volumn 134, Issue 8, 2012, Pages 3615-3618

Pd(II)/Brønsted acid catalyzed enantioselective allylic C-H activation for the synthesis of spirocyclic rings

Author keywords

[No Author keywords available]

Indexed keywords

C-H ACTIVATION; ENANTIOSELECTIVE; RING EXPANSION;

EID: 84857767521     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja2102407     Document Type: Article
Times cited : (185)

References (59)
  • 33
    • 67650553077 scopus 로고    scopus 로고
    • For a recent enantioselective total synthesis of (-)-acutumine
    • For a recent enantioselective total synthesis of (-)-acutumine: Li, F.; Tartakoff, S. S.; Castle, S. L. J. Am. Chem. Soc. 2009, 130, 6674
    • (2009) J. Am. Chem. Soc. , vol.130 , pp. 6674
    • Li, F.1    Tartakoff, S.S.2    Castle, S.L.3
  • 47
    • 70350346454 scopus 로고    scopus 로고
    • Phosphoric acid 1h and/or its silver salt have recently been shown to catalyze the semipinacol rearrangement of 2-oxo allylic alcohols to give chiral spirocyclic ethers
    • Phosphoric acid 1h and/or its silver salt have recently been shown to catalyze the semipinacol rearrangement of 2-oxo allylic alcohols to give chiral spirocyclic ethers: Zhang, Q.-W.; Fan, C.-A.; Zhang, H.-J.; Tu, Y.-Q.; Zhao, Y.-M.; Gu, P.; Chen, Z.-M. Angew. Chem., Int. Ed. 2009, 48, 8572
    • (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 8572
    • Zhang, Q.-W.1    Fan, C.-A.2    Zhang, H.-J.3    Tu, Y.-Q.4    Zhao, Y.-M.5    Gu, P.6    Chen, Z.-M.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.