Synthesis of selenolates from stannyl and silyl alkylselenides

Stannyl and silyl alkylselenides have been efficiently transformed to the corresponding alkylselenolates on reaction with butyllithiums. Other conditions proved to be limited.     

Three-component synthesis of benzo[b][1,5]thiazepines via coupling–addition–cyclocondensation sequence

2,4-Disubstituted benzo[b][1,5]thiazepines represent nonfluorescent intense yellow chromophores and are readily synthesized from acid chlorides, terminal alkynes, and ortho-amino thiophenols by a consecutive one-pot three-component Sonogashira coupling–Michael addition–cyclocondensation sequence under mild conditions in good yields.     

Decomposing torsion modules

E. Matlis proved that if R is an integral domain with quotient field Q and K is the R-module Q/R, then all torsion R-modules decompose into a direct sum of local submodules if and only if K decomposes into a direct sum of local submodules. Thus K is a test module to determine whether torsion modules decompose. We generalize this result to commutative rings. If R is a commutative ring and a torsion theory of R is given by a Gabriel topology , then form the ring of quotients R_ and let K be the cokernel of the canonical ring homomorphism from R to R_. In some special cases, every -torsion R-module decomposes into a direct sum of local submodules if and only if K decomposes. However, there is an example where this is not the case. The principal result is: given R,  and K, there is a related filter _K of ideals of R, which is a subset of , such that all _K-pretorsion R-modules decompose into a direct sum of local submodules if and only if K decomposes. The relationship between  and _K is investigated.     

Formation and Reactivity of Organo‐Functionalized Tin Selenide Clusters

Reactions of R¹SnCl₃ (R¹=CMe₂CH₂C(O)Me) with (SiMe₃)₂Se yield a series of organo‐functionalized tin selenide clusters, [(SnR¹)₂SeCl₄] ( 1 ), [(SnR¹)₂Se₂Cl₂] ( 2 ), [(SnR¹)₃Se₄Cl] ( 3 ), and [(SnR¹)₄Se₆] ( 4 ), depending on the solvent and ratio of the reactants used. NMR experiments clearly suggest a stepwise formation of 1 through 4 by subsequent condensation steps with the concomitant release of Me₃SiCl. Furthermore, addition of hydrazines to the keto‐functionalized clusters leads to the formation of hydrazone derivatives, [(Sn₂(μ‐R³)(μ‐Se)Cl₄] ( 5 , R³=[CMe₂CH₂CMe(NH)]₂), [(SnR²)₃Se₄Cl] ( 6 , R²=CMe₂CH₂C(NNH₂)Me), [(SnR⁴)₃Se₄][SnCl₃] ( 7 , R⁴=CMe₂CH₂C(NNHPh)Me), [(SnR²)₄Se₆] ( 8 ), and [(SnR⁴)₄Se₆] ( 9 ). Upon treatment of 4 with [Cu(PPh₃)₃Cl] and excess (SiMe₃)₂Se, the cluster fragments to form [(R¹Sn)₂Se₂(CuPPh₃)₂Se₂] ( 10 ), the first discrete Sn/Se/Cu cluster compound reported in the literature. The derivatization reactions indicate fundamental differences between organotin sulfide and organotin selenide chemistry.