1984
DOI: 10.1016/0003-2697(84)90791-7
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Synthesis and properties of 5-membered heterocyclic disulfides: Application for enzyme modification

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Cited by 11 publications
(1 citation statement)
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“…Solvents and reagents were appropriately dried and purified. 1,1'-Diisocyanoferrocene (1), [65] 1,1'-di (methylthio)ferrocene (4), [11] 1,1'-di(phenylthio)ferrocene (5), [11] 1,1'-di(2-thienyl)ferrocene (6), [10] 1,1',2,2'-tetra(methylthio)ferrocene (8), [66] 2,2'-di(thien-2-yl)disulfide, [67] 2,2'-di(thiazol-2-yl)disulfide [68] and 1,1'-bis(triphenylphosphoranylidenamino)ferrocene [8a] were prepared according to, or by slight variation of, published procedures. NMR: Varian Unity INOVA 500 (500.13 MHz for 1 H); IR: BIO-RAD FTS-40A; elemental analyses: microanalytical laboratories of the University of Kassel and of Imperial College London.…”
Section: Methodsmentioning
confidence: 99%
“…Solvents and reagents were appropriately dried and purified. 1,1'-Diisocyanoferrocene (1), [65] 1,1'-di (methylthio)ferrocene (4), [11] 1,1'-di(phenylthio)ferrocene (5), [11] 1,1'-di(2-thienyl)ferrocene (6), [10] 1,1',2,2'-tetra(methylthio)ferrocene (8), [66] 2,2'-di(thien-2-yl)disulfide, [67] 2,2'-di(thiazol-2-yl)disulfide [68] and 1,1'-bis(triphenylphosphoranylidenamino)ferrocene [8a] were prepared according to, or by slight variation of, published procedures. NMR: Varian Unity INOVA 500 (500.13 MHz for 1 H); IR: BIO-RAD FTS-40A; elemental analyses: microanalytical laboratories of the University of Kassel and of Imperial College London.…”
Section: Methodsmentioning
confidence: 99%