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Volumn 357, Issue 10, 2015, Pages 2219-2222

Rhodium-Catalyzed Addition of Alkyltrifluoroborate Salts to Imines

Author keywords

addition; enantiospecificity; imines; lactams; rhodium

Indexed keywords


EID: 84937239300     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201500295     Document Type: Article
Times cited : (11)

References (43)
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    • The stereochemistry of other products in Table 2 was assigned by analogy.
    • J. Escalante, M. A. González-Tototzin, Tetrahedron: Asymmetry 2003, 14, 981-985. The stereochemistry of other products in Table 2 was assigned by analogy.
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    • Escalante, J.1    González-Tototzin, M.A.2
  • 37
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    • The enantiospecificity can be calculated using the equation [% es=(ee of product/ee of starting material)×100], which indicates the degree of conservation of enantiomeric purity over the course of the reaction.
    • The enantiospecificity can be calculated using the equation [% es=(ee of product/ee of starting material)×100], which indicates the degree of conservation of enantiomeric purity over the course of the reaction:, S. E. Denmark, T. Vogler, Chem. Eur. J. 2009, 15, 11737-11745.
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    • The relative stereochemistry of addition product (8a) was determined by comparison with NMR data reported in the literature after deprotection.
    • The relative stereochemistry of addition product (8a) was determined by comparison with NMR data reported in the literature after deprotection, J. L. G. Ruano, J. Alemán, I. Alonso, A. Parra, V. Marcos, J. Aguirre, Chem. Eur. J. 2007, 13, 6179-6195.
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    • Ruano, J.L.G.1    Alemán, J.2    Alonso, I.3    Parra, A.4    Marcos, V.5    Aguirre, J.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.