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Volumn 80, Issue 20, 2015, Pages 9807-9816

Gold-Catalyzed Proto- and Deuterodeboronation

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSIS; CHEMICAL BONDS; GOLD;

EID: 84944884936     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/acs.joc.5b01041     Document Type: Article
Times cited : (27)

References (88)
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  • 2
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    • Certain organoboronic acids (e.g. 2-heteroarylboronic acids) are also susceptible to degradation via protodeboronation upon storage. See
    • Certain organoboronic acids (e.g., 2-heteroarylboronic acids) are also susceptible to degradation via protodeboronation upon storage. See: Noonan, G.; Leach, A. G. Org. Biomol. Chem. 2015, 13, 2555 10.1039/C4OB02543A
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    • 77951680625 scopus 로고    scopus 로고
    • For an example of arylboronic acids as nucleophiles in gold-catalyzed reactions, see
    • For an example of arylboronic acids as nucleophiles in gold-catalyzed reactions, see: Körner, C.; Starkov, P.; Sheppard, T. D. J. Am. Chem. Soc. 2010, 132, 5968 10.1021/ja102129c
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  • 37
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    • For a related allylation procedure using Pd catalysis and stoichiometric arylgold, see
    • For a related allylation procedure using Pd catalysis and stoichiometric arylgold, see: Pena-Lopez, M.; Ayan-Varela, M.; Sarandeses, L. A.; Sestelo, J. P. Org. Biomol. Chem. 2012, 10, 1686 10.1039/c2ob06788a
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  • 42
    • 84922344172 scopus 로고    scopus 로고
    • As far as the authors are aware, this is the first report of proto/deuterodeboronation using gold catalysis. For related gold-catalyzed protodecarboxylation, see
    • As far as the authors are aware, this is the first report of proto/deuterodeboronation using gold catalysis. For related gold-catalyzed protodecarboxylation, see: Dupuy, S.; Crawford, L.; Bühl, M.; Nolan, S. P. Chem.-Eur. J. 2015, 21, 3399 10.1002/chem.201405716
    • (2015) Chem. - Eur. J. , vol.21 , pp. 3399
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.