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Volumn 6, Issue 12, 2015, Pages 7319-7325

Chiral phosphine-catalyzed tunable cycloaddition reactions of allenoates with benzofuranone-derived olefins for a highly regio-, diastereo- and enantioselective synthesis of spiro-benzofuranones

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSIS; CYCLOADDITION; ENANTIOSELECTIVITY; OLEFINS; REGIOSELECTIVITY;

EID: 84946896288     PISSN: 20416520     EISSN: 20416539     Source Type: Journal    
DOI: 10.1039/c5sc03135d     Document Type: Article
Times cited : (80)

References (116)
  • 13
    • 84897976495 scopus 로고    scopus 로고
    • Selected papers on the phosphine-catalyzed cyclization of allenoates
    • Z. Wang X. Xu O. Kwon Chem. Soc. Rev. 2014 43 2927
    • (2014) Chem. Soc. Rev. , vol.43 , pp. 2927
    • Wang, Z.1    Xu, X.2    Kwon, O.3
  • 106
    • 84870359712 scopus 로고    scopus 로고
    • As for alkylidene azlactone, the γ-attack that initiated the asymmetric [3 + 2] cycloaddition with CP5 has been reported before (see ref. 13e). For mechanistic investigations, see
    • D. Uraguchi K. Yoshika Y. Ueki T. Ooi J. Am. Chem. Soc. 2012 134 19370
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 19370
    • Uraguchi, D.1    Yoshika, K.2    Ueki, Y.3    Ooi, T.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.