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Volumn 48, Issue 44, 2009, Pages 8361-8365

Tantalum-amidate complexes for the hydroaminoalkylation of secondary amines: enhanced substrate scope and enantioselective chiral amine synthesis

Author keywords

Amidates; Enantioselectivity Hydroaminoalkylation; Homogeneous catalysis; Tantalum

Indexed keywords

AMIDATE; AMIDATES; CHIRAL AMINES; ENANTIOSELECTIVE; HOMOGENEOUS CATALYSIS; HYDROGEN ABSTRACTION; SECONDARY AMINES; TANTALUM COMPLEXES;

EID: 70350004089     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200903656     Document Type: Article
Times cited : (144)

References (27)
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    • Angew. Chem. Int. Ed. 2009, 48, 4892-4894.
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 4892-4894
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    • 0842268019 scopus 로고    scopus 로고
    • Reviews on piperidine synthesis: a
    • Reviews on piperidine synthesis: a) M. G. P. Buffat, Tetrahedron 2004, 60, 1701-1729
    • (2004) Tetrahedron , vol.60 , pp. 1701-1729
    • Buffat, M.G.P.1
  • 26
    • 70350019146 scopus 로고    scopus 로고
    • See the Supporting Information for characterization data.
    • See the Supporting Information for characterization data.
  • 27
    • 70350013113 scopus 로고    scopus 로고
    • 13C NMR chemical shifts for a carbonyl group at approximately δ= 180 ppm.
    • 13C NMR chemical shifts for a carbonyl group at approximately δ= 180 ppm.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.