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Volumn 9, Issue 22, 2007, Pages 4407-4410

Acid-free, aminoborane-mediated Ugi-type reaction leading to general utilization of secondary amines

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EID: 35948970961     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol701570c     Document Type: Article
Times cited : (53)

References (32)
  • 1
    • 0003076580 scopus 로고
    • Reviews: a
    • Reviews: (a) Ugi, I. Angew. Chem. 1962, 74, 9-22;
    • (1962) Angew. Chem , vol.74 , pp. 9-22
    • Ugi, I.1
  • 4
    • 23744454427 scopus 로고    scopus 로고
    • Murahashi, S.-I, Ed, Thieme: Stuttgart
    • (c) Suginome, M.; Ito, Y. In Science of Synthesis; Murahashi, S.-I., Ed.; Thieme: Stuttgart, 2004; Vol. 19 pp 445-530.
    • (2004) Science of Synthesis , vol.19 , pp. 445-530
    • Suginome, M.1    Ito, Y.2
  • 5
    • 33847751116 scopus 로고    scopus 로고
    • Recent examples: (a) Trifilenkov, A. S.; Ilyin, A. P.; Kyrsil, V. M.; Sandulenko, Y. B.; Ivachtchenko, A. V. Tetrahedron Lett. 2007, 48, 2563-2567.
    • Recent examples: (a) Trifilenkov, A. S.; Ilyin, A. P.; Kyrsil, V. M.; Sandulenko, Y. B.; Ivachtchenko, A. V. Tetrahedron Lett. 2007, 48, 2563-2567.
  • 8
    • 34250857457 scopus 로고    scopus 로고
    • For recent examples of the use of isocyanides in organic synthesis, see: a
    • For recent examples of the use of isocyanides in organic synthesis, see: (a) Bonne, D.; Dekhane, M.; Zhu, J. Angew. Chem., Int. Ed. 2007, 46, 2485-2488.
    • (2007) Angew. Chem., Int. Ed , vol.46 , pp. 2485-2488
    • Bonne, D.1    Dekhane, M.2    Zhu, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.