메뉴 건너뛰기




Volumn 41, Issue 2, 2011, Pages 285-290

Development of an improved method for conversion of thiuram disulfides into N,N-dialkylcarbamoyl halides and derivatives

Author keywords

Carbon disulfide; N,N disubstituted carbamoyl halide; secondary amine; tetraalkyl thiuram disulfide

Indexed keywords

AMINE; CARBAMIC ACID DERIVATIVE; CARBON DISULFIDE; DISULFIRAM; N,N' DIALKYLCARBAMOYLCHLORIDE; ORGANIC SOLVENT; OXYGEN; UNCLASSIFIED DRUG;

EID: 78650255743     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910903537331     Document Type: Article
Times cited : (6)

References (19)
  • 1
    • 78650279443 scopus 로고    scopus 로고
    • Properties of dimethylcarbamoyl chloride
    • 87th ed.; CRC Press: Boca Raton, FL
    • Lide, D. R. Properties of dimethylcarbamoyl chloride. CRC Handbook of Chemistry and Physics, 87th ed.; CRC Press: Boca Raton, FL, 2006-2007.
    • (2006) CRC Handbook of Chemistry and Physics
    • Lide, D.R.1
  • 3
    • 37049090795 scopus 로고
    • 2-Protecting groups for 5-lithiation in the syntheses of imidazoles
    • Ngochindo, R. I. 2-Protecting groups for 5-lithiation in the syntheses of imidazoles. J. Chem. Soc., Perkin Trans. 1 1990, 1645-1648.
    • (1990) J. Chem. Soc, Perkin Trans. , vol.1 , pp. 1645-1648
    • Ngochindo, R.I.1
  • 4
    • 84986500842 scopus 로고
    • Benzimidazole condensed ring systems, 7: An entry to substituted 1h,6h-2,6a,10b-triazafluoranthene-1, 3,6-(2h)-triones and related systems as possible chemotherapeutic
    • El-Sayed, A. M.; Badawey, T. K. Benzimidazole condensed ring systems, 7: An entry to substituted 1h,6h-2,6a,10b-triazafluoranthene-1,3,6-(2h)-triones and related systems as possible chemotherapeutic. J. Heterocycl. Chem. 1991, 28, 995-998.
    • (1991) J. Heterocycl. Chem. , vol.28 , pp. 995-998
    • El-Sayed, A.M.1    Badawey, T.K.2
  • 6
    • 0001050031 scopus 로고
    • And coupling of pyrrole-1-carboxylic acid in the formation of pyrrole N-carbonyl compounds: Pyrrole-1-carboxylic acid anhydride
    • Boger, D. L.; Patel, M. Activation and coupling of pyrrole-1-carboxylic acid in the formation of pyrrole N-carbonyl compounds: Pyrrole-1-carboxylic acid anhydride. J. Org. Chem. 1987, 52(11), 2319-2323.
    • (1987) J. Org. Chem. , vol.52 , Issue.11 , pp. 2319-2323
    • Boger, D.L.1    Activation, P.M.2
  • 7
    • 0000921309 scopus 로고
    • Catalytic synthesis of O-b-oxoalkylcarbamates
    • Bruneau, C.; Dixncuf, P. H. Catalytic synthesis of O-b- oxoalkylcarbamates. Tetrahedron Lett. 1987, 28(18), 2005-2008.
    • (1987) Tetrahedron Lett. , vol.28 , Issue.18 , pp. 2005-2008
    • Bruneau, C.1    Dixncuf, P.H.2
  • 8
    • 0001390549 scopus 로고
    • Palladium-catalyzed generation of O-allylic urethanes and carbonates from amines=alcohols, carbon dioxide, and allylic chlorides
    • McGhee, W. D.; Riley, D. P.; Christ, M. E.; Christ, K. M. Palladium-catalyzed generation of O-allylic urethanes and carbonates from amines=alcohols, carbon dioxide, and allylic chlorides. Organometallics 1993, 12(4), 1429-1433.
    • (1993) Organometallics , vol.12 , Issue.4 , pp. 1429-1433
    • McGhee, W.D.1    Riley, D.P.2    Christ, M.E.3    Christ, K.M.4
  • 10
    • 3242757909 scopus 로고
    • A new synthesis of phthalides by internal trapping in ortho-lithiated carbamates derived from benzylic alcohol
    • Paleo, M. R.; Lamas, C.; Castedo, L. A new synthesis of phthalides by internal trapping in ortho-lithiated carbamates derived from benzylic alcohol. J. Org. Chem. 1992, 57(7), 2029-2033.
    • (1992) J. Org. Chem. , vol.57 , Issue.7 , pp. 2029-2033
    • Paleo, M.R.1    Lamas, C.2    Castedo, L.3
  • 11
    • 49549169494 scopus 로고
    • Reactions of arylcarbamoyl chlorides. II: Reaction with aromatic amines
    • Bacaloglu, R.; Bunton, C. A. Reactions of arylcarbamoyl chlorides, II: Reaction with aromatic amines. Tetrahedron 1973, 29, 2725-2730.
    • (1973) Tetrahedron , vol.29 , pp. 2725-2730
    • Bacaloglu, R.1    Bunton, C.A.2
  • 12
    • 0008389317 scopus 로고
    • Electrophilic reagents may react either with the hydroxyl group in position 3 or with the 2-nitrogen atom of 3-hydroxy-1, 2,4-thiadiazoles (1)
    • Taliani, L.; Pcrronnet, J. Electrophilic reagents may react either with the hydroxyl group in position 3, or with the 2-nitrogen atom of 3-hydroxy-1,2,4-thiadiazoles (1). J. Heterocycl. Chem. 1979, 16, 961-971.
    • (1979) J. Heterocycl. Chem. , vol.16 , pp. 961-971
    • Taliani, L.1    Pcrronnet, J.2
  • 13
    • 78650497990 scopus 로고
    • Friedel-Crafts reactions 3rd ed.; Wiley: New York
    • Friedel-Crafts reactions. Kirk-Othmer Encyclopedia of Chemical Technology, 3rd ed.; Wiley: New York 1982; 11 p. 286.
    • (1982) Kirk-Othmer Encyclopedia of Chemical Technology , vol.11 , pp. 286
  • 14
    • 4143150445 scopus 로고    scopus 로고
    • One-pot preparation of dialkylcarbamoyl azides from tertiary amines using triphosgene and sodium azide
    • Gumaste, V. K.; Dshmukh, A. R. A. S. One-pot preparation of dialkylcarbamoyl azides from tertiary amines using triphosgene and sodium azide. Tetrahedron Lett. 2004, 45(35), 6571-6573.
    • (2004) Tetrahedron Lett. , vol.45 , Issue.35 , pp. 6571-6573
    • Gumaste, V.K.1    Dshmukh, A.R.A.S.2
  • 17
    • 0000225475 scopus 로고
    • A centric thiuram disulfide: Structure of tetraisopropylthiuram disulfide
    • Kumar, V.; Aravamudan, G.; Seshasayee, M. A centric thiuram disulfide: Structure of tetraisopropylthiuram disulfide. Acta Cryst. 1990, C46, 674-676.
    • (1990) Acta Cryst. , vol.C46 , pp. 674-676
    • Kumar, V.1    Aravamudan, G.2    Seshasayee, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.