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Volumn 136, Issue 45, 2014, Pages 15837-15840

Asymmetric hydrogenation via capture of active intermediates generated from aza-pinacol rearrangement

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSIS; CYCLIZATION;

EID: 84910011179     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja5075745     Document Type: Article
Times cited : (27)

References (63)
  • 18
    • 79958819430 scopus 로고    scopus 로고
    • Enantioselective access to chiral 2,3-disubstituted indoline derivatives through consecutive Brønsted acid/Pd-complex-promoted reductive alkylation/hydrogenation was reported by us. The intermediate via Brønsted acid-catalyzed C-C bond-forming Friedel-Crafts reaction between indole and aldehyde is stable and separable. See: Duan, Y.; Chen, M.-W.; Ye, Z.-S.; Wang, D.-S.; Chen, Q.-A.; Zhou, Y.-G. Chem.-Eur. J. 2011, 17, 7193
    • (2011) Chem.-Eur. J. , vol.17 , pp. 7193
    • Duan, Y.1    Chen, M.-W.2    Ye, Z.-S.3    Wang, D.-S.4    Chen, Q.-A.5    Zhou, Y.-G.6
  • 20
    • 0003417469 scopus 로고
    • Trost, B. M. Fleming, I. Pergamon Press: Oxford, U.K
    • Rickborn, B. In Comprehensive Organic Synthesis; Trost, B. M.; Fleming, I., Eds.; Pergamon Press: Oxford, U.K., 1991; p 721.
    • (1991) Comprehensive Organic Synthesis , pp. 721
    • Rickborn, B.1
  • 63
    • 84910016569 scopus 로고    scopus 로고
    • CCDC 975090 contains the supplementary crystallographic data for product 2a. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • CCDC 975090 contains the supplementary crystallographic data for product 2a. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.