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Volumn 38, Issue 14, 1997, Pages 2463-2466

Iminyl radical generation via iminodithiocarbonate group transfer

Author keywords

[No Author keywords available]

Indexed keywords

RADICAL; THIOSEMICARBAZONE DERIVATIVE;

EID: 0030941642     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(97)00384-5     Document Type: Article
Times cited : (35)

References (17)
  • 8
    • 0003168906 scopus 로고    scopus 로고
    • (h) For a brief review, see:
    • (h) For a brief review, see: Zard, S.Z. Synlett 1996, 1148-1155.
    • (1996) Synlett , pp. 1148-1155
    • Zard, S.Z.1
  • 10
    • 0000643308 scopus 로고
    • For example, hydrazide 7b is made in one step from methylhydrazine, carbon disulfide, and methyl iodide whereas 7a requires the reaction of benzaldehyde phenylhydrazone with carbon disulfide and methyl iodide followed by heating with an equimolar amount of phenylhydrazine in ethanol/hydrochloric acid; see
    • For example, hydrazide 7b is made in one step from methylhydrazine, carbon disulfide, and methyl iodide whereas 7a requires the reaction of benzaldehyde phenylhydrazone with carbon disulfide and methyl iodide followed by heating with an equimolar amount of phenylhydrazine in ethanol/hydrochloric acid; see: Jensen, K.A.; Anthoni, U.; Holm, A. Acta Chem. Scand. 1969, 23, 1916-1934.
    • (1969) Acta Chem. Scand. , vol.23 , pp. 1916-1934
    • Jensen, K.A.1    Anthoni, U.2    Holm, A.3
  • 11
    • 0000556509 scopus 로고
    • We made a similar observation when we studied the reactions of S-triphenyltin xanthates
    • We made a similar observation when we studied the reactions of S-triphenyltin xanthates: Boivin, J.; Camara, J.; Zard, S.Z. Zard J. Am. Chem. Soc. 1992, 114, 7909-7910.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 7909-7910
    • Boivin, J.1    Camara, J.2    Zard, S.Z.3    Zard4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.