Structural and Mössbauer effect investigations of amorphous FeCuNbSiB alloys nanocrystallized (VITROPERM) in magnetic field.

Melt-spun amorphous ribbons of nominal composition Fe73Cu1Nb3Si16B7, annealed at 560-580 degrees C for 1 hour in a magnetic field (H) applied along the width in the ribbon plane, develop uniaxial magnetic anisotropy with easy axis along H and exhibit several novel attributes. The samples labelled as S20 and S150 are nanocomposites consisting of ferromagnetic nanocrystalline grains (volume fraction approximately equal to 84% and 81%) of mean size d = 13(2) nm embedded in a ferromagnetic amorphous matrix and possess a magnetic permeability as large as 20,000 and 150,000, respectively. While nearly 55% of the nanocrystalline grains have a cubic DO3 Fe3Si-like structure with actual Si concentration of about 22 at.

A new entry to polycyclic indole derivatives via intramolecular imino Diels-Alder reaction: observation of unexpected reaction.

A new, efficient, and highly diastereoselective synthesis of polycyclic indole derivatives through intramolecular imino Diels-Alder reaction of aminoanthraquinone with N-prenylated indole-2-carboxaldehydes in the presence of 20 mol % of triphenylphosphonium perchlorate (TPPP) is reported with extremely high cis selectivity in good yield.

Red-, blue-, or no-shift in hydrogen bonds: a unified explanation.

We provide a simple explanation for X-H bond contraction and the associated blue shift and decrease of intensity in IR spectrum of the so-called improper hydrogen bonds. This explanation organizes hydrogen bonds (HBs) with a seemingly random relationship between the X-H bond length (and IR frequency and its intensity) to its interaction energy. The factors which affect the X-H bond in all X-H.

Conversion of propargyl alcohols to chloroallenes and arylalkynes using the TiCl4/R3N reagent system.

Whereas the reaction of certain propargyl alcohols with TiCl4 in the presence of tertiary alkylamines gives the corresponding chloroallenes in 37-58% yields, reaction with the tertiary arylamines gives the corresponding arylalkynes in 68-77% yields.

A simple method of synthesis of (+/-)-2,3-diarylpiperazines and a novel method of resolution of (+/-)-2,3-diphenylpiperazine.

Intramolecular reductive coupling of diimines in the presence of Zn/Ti(O(i)Pr)2Cl2 gives the corresponding (+/-)-2,3-diarylpiperazines in 73-83% yields with dl/meso ratio >99%:<1%. The (+/-)-2,3-diphenylpiperazine obtained in this way was readily resolved partially using L-(+)-tartaric acid, and the enantiomeric purity was enhanced to >99% ee via preparation of hydrogen-bonded salt aggregates using oxalic acid.

Simple and efficient methods of synthesis of 3,3-diarylcyclobutanone and 3,3-diarylcyclobutylamine derivatives using the TiCl4/R3N reagent system.

[reaction: see text] The iminium ions generated in situ by the oxidation of N,N-diisopropyl-N-benzylamine using iodine react with diaryl ketones in the presence of TiCl4/R3N to give the corresponding 3,3-diarylcyclobutanones in moderate to good yields (49-86%). The 3,3-diarylcyclobutanone iminium ions formed in this transformation was reduced in situ with B2H6 to produce the corresponding 3,3-diarylcyclobutylamines (52-79% yields), a class of compounds with potential antidepressant activity. In addition, a series of N,N-dimethyl-3,3-diarylcyclobutylamines were synthesized by the reductive amination of the corresponding 3,3-diarylcyclobutanone derivatives.

Toward homogeneity of chirality via selective formation of homochiral or heterochiral aggregates.

[reaction: see text] A new method of achieving homogeneity of chirality via purification of nonracemic (partially resolved) amino alcohols 1a-d and the C2 chiral diamine 2 to obtain samples of higher ee, through preparation of homochiral and heterochiral aggregates using oxalic and fumaric acids, is described.

New methods of resolution and purification of racemic and diastereomeric amino alcohol derivatives using boric acid and chiral 1,1'-bi-2-naphthol.

Resolution of the racemic amino alcohol derivatives 1-6 is readily achieved to obtain enantiomerically enriched compounds using chiral 1,1'-bi-2-naphthol and boric acid in solvents such as CH(3)CN, THF, and MeOH. Purification of the diastereomeric mixture 7 has also been carried out following this method. The corresponding intermediate ammonium borate complexes were also characterized by X-ray diffraction methods.

New Methods of Resolution and Enrichment of Enantiomeric Excesses of 1,1'-Bi-2-naphthol.

Partial resolution of racemic 1,1'-bi-2-naphthol (1) was readily achieved to obtain enriched (scalemic) 1 using (S)-proline (2). The structure of the complex 3 formed between 1 (2 equiv) and (S)-proline (1 equiv) was characterized by an X-ray diffraction method. Enantiomeric excesses of the incompletely resolved 1 were enriched to obtain essentially pure (R)- and (S)-1 following a simple procedure using B(OH)(3) and TMEDA.