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Volumn 33, Issue 19, 2003, Pages 3405-3410

A convenient procedure for the preparation of oxime chloroformates

Author keywords

[No Author keywords available]

Indexed keywords

KETOXIME; O (CHLOROFORMYL)OXIME; OXIME CHLOROFORMATE; OXIME DERIVATIVE; PHOSGENE; REAGENT; UNCLASSIFIED DRUG;

EID: 0041832073     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1081/SCC-120023999     Document Type: Article
Times cited : (3)

References (9)
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    • (1967) Z. Chem. , vol.9 , pp. 344-345
    • Jumar, A.1    Held, P.2    Schulze, W.3
  • 2
    • 0025681060 scopus 로고
    • Preparation and Beckmann rearrangement of O-(chlorooxalyl)oximes
    • Jochims, Johannes C.; Hehl, S.; Herzberger, S. Preparation and Beckmann rearrangement of O-(chlorooxalyl)oximes. Synthesis 1990, 12, 1128-1133.
    • (1990) Synthesis , vol.12 , pp. 1128-1133
    • Jochims, J.C.1    Hehl, S.2    Herzberger, S.3
  • 3
    • 4243902242 scopus 로고
    • Darstellung und thermolyse von O-tert-butylperoxycarbonylketoximen
    • Rüchardt, Ch.; Pantke, R. Darstellung und Thermolyse von O-tert-Butylperoxycarbonylketoximen. Chem. Ber. 1971, 104, 3456-3462.
    • (1971) Chem. Ber. , vol.104 , pp. 3456-3462
    • Rüchardt, Ch.1    Pantke, R.2
  • 4
    • 0034622304 scopus 로고    scopus 로고
    • Improved procedures for the Beckmann rearrangement: The reaction of ketoxime carbonates with boron trifluoride etherate
    • Anilkumar, R.; Chandrasekhar, S. Improved procedures for the Beckmann rearrangement: the reaction of ketoxime carbonates with boron trifluoride etherate. Tetrahedron Lett. 2000, 41, 5427-5429.
    • (2000) Tetrahedron Lett. , vol.41 , pp. 5427-5429
    • Anilkumar, R.1    Chandrasekhar, S.2
  • 5
    • 84985534727 scopus 로고
    • Triphosgene, a crystalline phosgene substitute
    • Eckert, H.; Forster, B. Triphosgene, a crystalline phosgene substitute. Angew. Chem. Int. Ed. Engl. 1987, 26 (9), 894-895.
    • (1987) Angew. Chem. Int. Ed. Engl. , vol.26 , Issue.9 , pp. 894-895
    • Eckert, H.1    Forster, B.2
  • 6
    • 0027454802 scopus 로고
    • A safe and efficient method for conversion of 1,2-and 1,3-diols to cyclic carbonates utilizing triphosgene
    • Burk, Robert M.; Roof, Michael B. A safe and efficient method for conversion of 1,2-and 1,3-diols to cyclic carbonates utilizing triphosgene. Tetrahedron Lett. 1993, 34 (3), 395-398.
    • (1993) Tetrahedron Lett. , vol.34 , Issue.3 , pp. 395-398
    • Burk, R.M.1    Roof, M.B.2
  • 7
    • 0024353698 scopus 로고
    • Cobalt-mediated reactions. A new synthetic approach to β-, γ- and δ-lactams
    • Gill, G.B.; Pattenden, G.; Reynolds, Stephen J. Cobalt-mediated reactions. A new synthetic approach to β-, γ- and δ-lactams. Tetrahedron Lett. 1989, 30 (24), 3229-3232.
    • (1989) Tetrahedron Lett. , vol.30 , Issue.24 , pp. 3229-3232
    • Gill, G.B.1    Pattenden, G.2    Reynolds, S.J.3
  • 8
    • 0026353192 scopus 로고
    • Facile chloride substitution of activated alcohols by triphosgene: Application to cephalosporin chemistry
    • Goren, Z.; Heeg, Mary J.; Mobashery, S. Facile chloride substitution of activated alcohols by triphosgene: application to cephalosporin chemistry. J. Org. Chem. 1991, 56 (25), 7186-7188.
    • (1991) J. Org. Chem. , vol.56 , Issue.25 , pp. 7186-7188
    • Goren, Z.1    Heeg, M.J.2    Mobashery, S.3
  • 9
    • 0041564903 scopus 로고
    • Synthesen mit hilfe des dipyridiniumsalzes des phosgens
    • Scholtissek, Ch. Synthesen mit Hilfe des Dipyridiniumsalzes des Phosgens. Chem. Ber. 1956, 89 (11), 2562-2565.
    • (1956) Chem. Ber. , vol.89 , Issue.11 , pp. 2562-2565
    • Scholtissek, Ch.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.