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1.
Barium     
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In the first section we summarize some properties of Jordan pairs. Then we state some results about some groups defined by Jordan pairs.In the next section we construct a Lie algebra to a Jordan pair. This construction is a generalization of the wellknown Koecher-Tits-construction. We calculate the radical of this Lie algebra in terms of the given Jordan pair.In the last section we prove a Wedderburn decomposition theorem for Jordan pairs in the characteristic zero case. Some special cases in arbitrary characteristic have been shown by R. Carlson (see [5]). Also we show that any two such decompositions are conjugate under a certain group of automorphism. Analogous theorems will be shown for Jordan Triples.  相似文献   
3.
Diphenyl phosphorazidate (DPPA) was used as the azide source in a one-pot synthesis of 2,2-disubstituted 3-amino-2H-azirines 1 (Scheme 1). The reaction with lithium enolates of amides of type 2 , bearing two substituents at C(2), proceeded smoothly in THF at 0°; keteniminium azides C and azidoenamines D are likely intermediates. Under analogous reaction conditions, DPPA and amides of type 3 with only one substituent at C(2) gave 2-diazoamides 5 in fair-to-good yield (Scheme 2). The corresponding 2-diazo derivatives 6–8 were formed in low yield by treatment of the lithium enolates of N,N-dimethyl-2-phenylacetamide, methyl 2-phenylacetate, and benzyl phenyl ketone, respectively, with DPPA. Thermolysis of 2-diazo-N-methyl-N-phenylcarboxamides 5a and 5b yielded 3-substituted 1,3-dihydro-N-methyl-2H-indol-2-ones 9a and 9b , respectively (Scheme 3). The diazo compounds 5–8 reacted with 1,3-thiazole-5 (4H)-thiones 10 and thiobenzophenone ( 13 ) to give 6-oxa-1,9-dithia-3-azaspiro[4.4]nona-2,7-dienes 11 (Scheme 4) and thiirane-2-carboxylic acid derivatives 14 (Scheme 5), respectively. In analogy to previously described reactions, a mechanism via 1,3-dipolar cycloaddition, leading to 2,5-dihydro-1,3,4-thiadiazoles, and elimination of N2 to give the ‘thiocarbonyl ylides’ of type H or K is proposed. These dipolar intermediates with a conjugated C?O group then undergo either a 1,5-dipolar electrocyclization to give spirohetrocycles 11 or a 1,3-dipolar electrocyclization to thiiranes 14 .  相似文献   
4.
Novel rhenium(I) tricarbonyl complexes have been prepared by reactions of (Et4N)2[Re(CO)3Br3] with acetylpyridine benzoylhydrazone, Hapbhyd, di(2‐pyridyl)ketone benzoylhydrazone, Hpy2bhyd, bis(2‐pyridine)ketone, py2CO, and pyridinealdehyde terephtalaldehydebishydrazone, pytehyd. The ligands remain protonated when no supporting base is added and the following complexes have been isolated: [Re(CO)3Br(Hapbhyd)], [Re(CO)3Br(Hpy2bhyd‐py, hyd)], [Re(CO)3Br(Hpy2bhyd‐py1, py2)], [Re(CO)3Br(py2CO‐N, N)] and [Re(CO)3Br(pytehyd)]. Addition of triethyl amine results in deprotonation of Hapbhyd and the formation of [Re(CO)3(OH2)(apbhyd)], whereas Hpy2bhyd is hydrolysed and a rhenium complex with the monoanionic bis(2‐pyridyl)hydroxymethanolato ligand, {py2C(OH)O}, is formed. The same compound, [Re(CO)3{py2C(OH)O}], is obtained when triethyl amine and water are added to a mixture of (Et4N)2[Re(CO)3Br3] and py2CO. The air‐stable products have been studied by spectroscopic methods and X‐ray crystallography.  相似文献   
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Alajlani  Muaaz  Shiekh  Abid  Hasnain  Shahida  Brantner  Adelheid 《Chromatographia》2016,79(21):1527-1532

Bacillus subtilis strain BIA was used for the production of bioactive lipopeptides. Different extraction and purification methods were assayed as liquid–liquid extraction, and acid and ammonium sulfate precipitation followed by TLC, SPE, and gel filtration. Active fractions were further purified using RP-HPLC. The molecular mass of the purified product from HPLC was determined through Tris-Tricine SDS-PAGE and MALDI–TOF-MS. The results revealed that Bacillus subtilis strain BIA produced surfactin and iturin like compounds. Coproduction of surfactin and iturin like compounds by this strain is a remarkable trait for a potential biocontrol agent. This paper also includeds techniques that have been developed for the optimal and convenient extraction of bioactive lipopeptides from microbial origin.

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