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Volumn 12, Issue 26, 2006, Pages 6991-6996

Gold catalysis: No steric limitations in the phenol synthesis

Author keywords

Cyclization; Dihydroisoindoles; Gold; Homogeneous catalysis; Tetrahydroisoquinolines

Indexed keywords

FURAN RESINS; GOLD; HUMAN REACTION TIME; PHENOLS;

EID: 33748621454     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200600533     Document Type: Article
Times cited : (94)

References (36)
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    • Even a recent example of a gold-catalyzed Pictet-Spengler reaction only showed the selectivity known for other Lewis acids and Brønsted acids: S. W. Youn, J. Org. Chem. 2006, 71, 2521-2523.
    • (2006) J. Org. Chem. , vol.71 , pp. 2521-2523
    • Youn, S.W.1
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    • CCDC-603475 (26b), CCDC-603474 (28a), CCDC-603476 (28b), and CCDC-603477 (28 e) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from the Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.
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    • Wiley-VCH, 20th ed., Weinheim, procedure C
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.