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Volumn 52, Issue 44, 2013, Pages 11577-11580

Selective reduction of amides to amines by boronic acid catalyzed hydrosilylation

Author keywords

amides; boron; homogeneous catalysis; organocatalysis; reduction

Indexed keywords

BORONIC ACID; HOMOGENEOUS CATALYSIS; HYDROSILANES; ORGANOCATALYSIS; PRIMARY AMIDES; SELECTIVE REDUCTION;

EID: 84885978163     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201304495     Document Type: Article
Times cited : (101)

References (56)
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    • Tan, M.1    Zhang, Y.2
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    • Renzi, P.1    Bella, M.2
  • 45
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    • in, (Eds.: H. Steinberg, A. L. McCloskey), Pergamon, New York
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    • When the compound below (10 mol %) was used as the catalyst, no reaction occurred. Notably 3 k is much less efficient compared to 3 i and 3 j, and highlights the impact of the benzothiophene moiety. For the additive effect of benzothiophene derivatives, see Scheme S5. For details, see the Supporting Information. For the use of thiophene derivatives to promote hydrosilylation of ketones, see:, A. Furuta, H. Nishiyama, Tetrahedron Lett. 2008, 49, 110.
    • (2008) Tetrahedron Lett. , vol.49 , pp. 110
    • Furuta, A.1    Nishiyama, H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.