Results 181 to 190 of about 23,536 (214)
Synthesis of α-Amino Isocyanides and α-Alkylthio Isocyanides [PDF]
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Alan R. Katritzky +2 more
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Journal of the American Chemical Society, 1978
H/sub 2/Os/sub 3/(CO)/sub 10/ was reacted with phenyl isocyanide to form H/sub 2/Os/sub 3/(CO)/sub 10/(CNC/sub 6/H/sub 5/), which upon refluxing loses 1 mol CO to form a new complex that is believed to be a possible intermediate in the phenyl isocyanide reduction process. The molecular structure of the last complex was determined. (DLC)
Richard D. Adams, Nancy M. Golembeski
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H/sub 2/Os/sub 3/(CO)/sub 10/ was reacted with phenyl isocyanide to form H/sub 2/Os/sub 3/(CO)/sub 10/(CNC/sub 6/H/sub 5/), which upon refluxing loses 1 mol CO to form a new complex that is believed to be a possible intermediate in the phenyl isocyanide reduction process. The molecular structure of the last complex was determined. (DLC)
Richard D. Adams, Nancy M. Golembeski
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Multicomponent Reactions with Isocyanides
Angewandte Chemie, 2000Multicomponent reactions (MCRs) are fundamentally different from two-component reactions in several aspects. Among the MCRs, those with isocyanides have developed into popular organic-chemical reactions in the pharmaceutical industry for the preparation of compound libraries of low-molecular druglike compounds.
Alexander Dömling, Ivar Ugi
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Microchemical detection of isocyanides
Talanta, 1967Microgram quantities of isocyanides may be easily detected on filter paper or in tubes of silica gel by using benzidine acetate-copper(II) acetate or p,p'-tetramethyldiaminodiphenylmethane-copper(II) sulphate reagents. Interferences include those substances which are known to interfere in the use of the same reagents for the detection of hydrogen ...
Edward J. Poziomek +2 more
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2,4,6-Trimethylphenyl isocyanide
Acta Crystallographica Section C Crystal Structure Communications, 2002The title compound, C(10)H(11)N, displays a crystallographic mirror plane that incorporates all the non-H atoms, as well as the H atoms attached to the aromatic ring. The isocyano group is almost linear and shows an N[triple bond]C bond distance of 1.158 (3) A.
Marcus Layh +2 more
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The photoelectron spectra of methyl isocyanide and trideutero-methyl isocyanide
Spectrochimica Acta Part A: Molecular Spectroscopy, 1971Abstract The photoelectron spectra of methyl isocyanide and its d3- analogue have been measured. Ionisation potentials from three molecular orbitals in each case have been determined in the range 6–20eV, and the nature of these orbitals has been suggested from a consideration of the vibrations excited during the ionisation processes.
Harold Warris Thompson, R.F. Lake
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The Nef Reaction of Isocyanides
Synthesis, 2014AbstractReview: [58 refs.
La Spisa, Fabio +2 more
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Isocyanides and Their Heteroanalogs (RZC)
ChemInform, 2005AbstractFor Abstract see ChemInform Abstract in Full Text.
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Acta Crystallographica Section C Crystal Structure Communications, 2004
Achiral p-nitrophenyl isocyanide, C(7)H(4)N(2)O(2), crystallizes in the orthorhombic chiral space group P2(1)2(1)2(1). Attractive intermolecular interactions between the nitro O atoms and both aromatic H and nitro N atoms of neighbouring molecules are observed.
Allen D. Hunter, Matthias Zeller
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Achiral p-nitrophenyl isocyanide, C(7)H(4)N(2)O(2), crystallizes in the orthorhombic chiral space group P2(1)2(1)2(1). Attractive intermolecular interactions between the nitro O atoms and both aromatic H and nitro N atoms of neighbouring molecules are observed.
Allen D. Hunter, Matthias Zeller
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Syntheses of Isocyanide Dihalides [PDF]
AbstractThe methods for the preparation of isocyanide dihalides, and particularly of isocyanide dichlorides, are described. The scopes and courses of the various processes are critically discussed.
Engelbert Kuhle, G. Zumach, B. Anders
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