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Volumn 9, Issue 25, 2007, Pages 5155-5157

Catalytic enantioselective addition of arylboronic acids to N-Boc imines generated in situ

Author keywords

[No Author keywords available]

Indexed keywords

BORONIC ACID DERIVATIVE; IMINE;

EID: 37249065123     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol702045w     Document Type: Article
Times cited : (64)

References (20)
  • 10
    • 33847620405 scopus 로고    scopus 로고
    • For a comprehensive review on reactivity and properties of activated imines see
    • For a comprehensive review on reactivity and properties of activated imines see: Petrini, M.; Torregiani, E. Synthesis 2007, 159-186.
    • (2007) Synthesis , pp. 159-186
    • Petrini, M.1    Torregiani, E.2
  • 16
    • 37249010844 scopus 로고    scopus 로고
    • To our knowledge, the addition of arylboronic acids to activated imines generated in situ has not previously been reported
    • To our knowledge, the addition of arylboronic acids to activated imines generated in situ has not previously been reported.
  • 17
    • 29144448796 scopus 로고    scopus 로고
    • For in situ generation of N-Boc imines in an aza-Henry reaction see: Fini, F.; Sgarzani, V.; Pettersen, D.; Herrera, R. P.; Bernardi, L. Ricci, A. Angew. Chem., Int. Ed. 2005, 44, 7975-7978.
    • For in situ generation of N-Boc imines in an aza-Henry reaction see: Fini, F.; Sgarzani, V.; Pettersen, D.; Herrera, R. P.; Bernardi, L. Ricci, A. Angew. Chem., Int. Ed. 2005, 44, 7975-7978.
  • 18
    • 0000652292 scopus 로고    scopus 로고
    • DeguPHOS is available from a number of chemical suppliers, including Strem Chemicals, Inc., ACBR GmbH KG, and Degussa AG. Nagel, U.; Kinzel, E.; Andrade, J.; Prescher, G. Chem. Ber. 1986, 119, 3326-3343.
    • DeguPHOS is available from a number of chemical suppliers, including Strem Chemicals, Inc., ACBR GmbH KG, and Degussa AG. Nagel, U.; Kinzel, E.; Andrade, J.; Prescher, G. Chem. Ber. 1986, 119, 3326-3343.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.