7519-74-6Relevant articles and documents
Regioselective monohalogenation of 3,3-disubstituted bornane-2-thiones via thione-dihalogen complexes
Shimada, Kazuaki,Nanae, Takashi,Aoyagi, Shigenobu,Takikawa, Yuji,Kabuto, Chizuko
, p. 6167 - 6169 (2001)
Reaction of 3,3-disubstituted bornane-2-thiones with Br2, ICl, or Cl2 afforded the corresponding 10-bromobornane-2-thiones, 10-iodobornane-2-thiones, or the products originated from skeletal rearrangement of 10-chlorobornane-2-thiones, respectively.
Studies on the preparation of camphorylidene derivatives of α-amino acids
Gamble, David L.,Hems, William P.,Ridge, Brian
, p. 248 - 260 (2007/10/03)
An improved method has been developed for the efficient synthesis of stable camphor imine salts. Camphor imine readily undergoes transimination with α-amino acid ester hydrochlorides to yield camphorylidene amino acid derivatives with E stereochemistry about the C=N double bond. Sodium cyanoborohydride reduction of the derived ketimines gives exo-bornylamines.
Blue Copper Models. Synthesis and Characterization of Copper(II) Enethiolate Complexes derived from (1R)-3-Hydroxymethylenebornane-2-thione and 2-Aminothia-alkyl-1-methylbenzimidazoles (Donor Set N2SS*) or Diamines (Donor Set N2S2)
Casella, Luigi,Gullotti, Michele,Suardi, Edoardo,Sisti, Massimo,Pagliarin, Roberto,Zanello, Piero
, p. 2843 - 2851 (2007/10/02)
A series of tetradentate ligands derived from the condensation of (1R)-3-hydroxymethylenebornane-2-thione and several 2-aminothia-alkylbenzimidazoles were synthesized together with their cationic zinc(II) and copper(II) complexes.While the free ligands exist in the thioxoenamine tautomeric form, binding to the metals occurs in their enethiolateimine form, as deduced from cumulative spectral evidence.The copper(II) complexes exhibit medium-intensity absorptions between 410 and 435 (ε 3500) and between 520 and 535 nm (ε 1200 dm3 mol-1 cm-1) attributable to enethiolate ?(S-) --> CuII and ?(S-) --> CuII ligand-to-metal charge transfer (l.m.c.t.) transitions, respectively, and relatively intense ligand-field transitions in the range 610-650 nm (ε 1500 dm3mol-1cm-1).All the bands undergo progressive red shift as the length of the carbon chain connecting the imine and thioether functions increases from two to four atoms.The frozen-solution e.p.r. spectra are indicative of progressive distortion towards a pseudo-tetrahedral geometry for copper(II) as the carbon chain length increases.A series of neutral copper(II) complexes derived from the condensation of (1R)-3-hydroxymethylenebornane-2-thione and symmetric diamines was also synthesized for comparison.Here too the length of the carbon chain connecting the imine nitrogen atoms was varied from two to four atoms.These complexes exhibit the same spectroscopic trends but with less marked distortion of the copper(II) chromophores as the length of the carbon chain increases.The cationi copper (II) complexes from (1R)-3-hydroxy-methylenebornane-2-thione and 2-aminothia-alkylbenzimidazoles display, in acetonitrile solution at -15 deg C, easy access to the corresponding copper(I) congeners (E0=-0.02V vs s.c.e.).By contrast, the neutral copper(II) species derived from (1R)-3-hydroxymethylenebornane-2-thione and diamines are reduced to the corresponding copper(I) complexes at potentials more negative by 0.7-1.0 V, depending upon the extent of stereochemical distortion around the copper(II) centre induced by the length of the imine-nitrogen-linking carbon chain.The planar complex bearing an ethylene bridging chain can be reversibly oxidized to the corresponding copper(III) species (E0= +0.37 V).
