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Volumn 57, Issue 21, 2001, Pages 4623-4627

Synthesis of a new optically active carbamoyl azide and its use as an aminating agent

Author keywords

Amination; Amino ketones; Asymmetric reactions; Oxazolines

Indexed keywords

ALKENE; AZIDE; CARBAMOYL AZIDE; KETONE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0035927189     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(01)00383-0     Document Type: Article
Times cited : (15)

References (26)
  • 1
    • 84956794765 scopus 로고    scopus 로고
    • For a very recent review, see: A. Ricci. Weinheim: Wiley-VCH
    • For a very recent review, see: Ricci A. Modern Amination Methods. 2000;Wiley-VCH, Weinheim.
    • (2000) Modern Amination Methods
  • 13
    • 0030718554 scopus 로고    scopus 로고
    • Asymmetric cyclopropanation by an Oppolzer's sultam carbenoid was reported:
    • Asymmetric cyclopropanation by an Oppolzer's sultam carbenoid was reported: Haddad N., Galili N. Tetrahedron: Asymmetry. 8:1997;3367-3370.
    • (1997) Tetrahedron: Asymmetry , vol.8 , pp. 3367-3370
    • Haddad, N.1    Galili, N.2
  • 14
    • 0343049646 scopus 로고    scopus 로고
    • CAUTION: Reactions involving azides are capable of being explosive. While we have experienced no problems, care should be exercised
    • CAUTION: Reactions involving azides are capable of being explosive. While we have experienced no problems, care should be exercised.
  • 17
    • 0013473360 scopus 로고
    • For the reactivity of norbornene in the presence of different azides, see:
    • For the reactivity of norbornene in the presence of different azides, see: Subbaraj A., Subba Rao O., Lwowski W. J. Org. Chem. 54:1989;3945-3952.
    • (1989) J. Org. Chem. , vol.54 , pp. 3945-3952
    • Subbaraj, A.1    Subba Rao, O.2    Lwowski, W.3
  • 18
    • 0030873707 scopus 로고    scopus 로고
    • We isolated similar products by the cycloaddition reactions of different azides on sterically hindered enamines:
    • We isolated similar products by the cycloaddition reactions of different azides on sterically hindered enamines: Fioravanti S., Pellacani L., Ricci D., Tardella P.A. Tetrahedron: Asymmetry. 8:1997;2261-2266.
    • (1997) Tetrahedron: Asymmetry , vol.8 , pp. 2261-2266
    • Fioravanti, S.1    Pellacani, L.2    Ricci, D.3    Tardella, P.A.4
  • 22
    • 0025601635 scopus 로고
    • The configuration of the major diastereomer was established by comparison with the same product obtained by elaboration of the appropriate optically pure trans-1,2-amino alcohol, according to a reported procedure:
    • The configuration of the major diastereomer was established by comparison with the same product obtained by elaboration of the appropriate optically pure trans-1,2-amino alcohol, according to a reported procedure: Fioravanti S., Loreto M.A., Pellacani L., Tardella P.A. Tetrahedron: Asymmetry. 1:1990;931-936.
    • (1990) Tetrahedron: Asymmetry , vol.1 , pp. 931-936
    • Fioravanti, S.1    Loreto, M.A.2    Pellacani, L.3    Tardella, P.A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.