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1.
The Mathematical Intelligencer encourages comments about the material in this issue. Letters to the editor should be sent
to either of the editors-in-chief, Chandler Davis or Marjorie Senechal. 相似文献
2.
Gregory N. Coppin Andrew Hudson Richard A. Jackson Nigel P.C. Simmons 《Journal of organometallic chemistry》1977,131(3):371-375
The formation of the compound RSnX(acac)2 (acac = 2,4-pentanedionato) by reaction of bis(2,4-pentanedionato)tin(II) on a halide RX with R = CH3, C2H5, C4H9, C6H5, CH2I, (C6H5)3SnCH2, (C2H5)3SnCH2 and X = I, Br has been studied by polarography. At 25°C, it is in fact an equilibrium whose constant has been measured. The intermediate formation of the ion-pair [RSn(acac)2+X?] has allowed us to explain the experimental results. 相似文献
3.
4.
5.
Jerald S. Bradshaw Reed M. Izatt James J. Christensen Krzystof E. Krakowiak Bryon J. Tarbet Ronald L. Bruening S. Lifson 《Journal of inclusion phenomena and macrocyclic chemistry》1989,7(2):127-136
Silica gel-bound crown ethers and aza macrocycles have been synthesized with the attaching arm connected to the carbon framework of the macrocycles. The interactions of these bound macrocycles with cations are almost identical to those involving the analogous free macrocycles. This has allowed for predictable cation separation, concentration, and removal processes to be performed on a small scale. Quantum mechanical calculations and NMR measurements indicate that similarly bound chiral macrocycles will be capable of use in separating chiral organic amines.Dedicated to the memory of Professor James J. Christensen who died on 5 September 1987. 相似文献
6.
Christian Margot DanaP. Simmons Daniel Reichlin David Skuy 《Helvetica chimica acta》2004,87(10):2662-2684
Only one out of the four possible trans isomers of the important perfumery alcohol Norlimbanol® ( 1 ) possesses a very strong amber‐woody smell, the isomer 1A with (1′R,3S,6′S) absolute configuration. Its enantiomer 1B is almost odorless and devoid of amber‐woody character, whereas the diastereoisomers 1C and 1D are considerably weaker and perceptible only by the most‐sensitive persons. The same is true for a whole series of perceptual analogs of 1 , including β‐alkoxy alcohols. These ethers belong to two structural classes: [(2,2,6‐trimethylcyclohexyl)oxy]‐ (see 3, 4 , and 16 ) or {[2‐(tert‐butyl)cyclohexyl]oxy}alkan‐2‐ol derivatives (see 19 and 20 ; Table). A superimposition model allowing for good overlap of the respective hydroxylated side chains offers a tentative explanation for the shared perceptual characteristics of the two classes (Fig. 5). The lipophilic cyclohexane moieties present only a minimal overlap in this model, suggesting that quite larger molecules might possess the same smell. (S)‐Configured β‐alkoxy alcohols can conveniently be obtained on a larger scale by enantioselective reduction of the corresponding ketones (Scheme 9). 相似文献
7.
Erlanson DA McDowell RS He MM Randal M Simmons RL Kung J Waight A Hansen SK 《Journal of the American Chemical Society》2003,125(19):5602-5603
Protein tyrosine phosphatases play important roles in many signaling cascades involved in human disease. The identification of druglike inhibitors for these targets is a major challenge, and the discovery of suitable phosphotyrosine (pY) mimetics remains one of the key difficulties. Here we describe an extension of tethering technology, "breakaway tethering", which is ideally suited for discovering such new chemical entities. The approach involves first irreversibly modifying a protein with an extender that contains both a masked thiol and a known pY mimetic. The extender is then cleaved to release the pY mimetic, unmasking the thiol. The resulting protein is screened against a library of disulfide-containing small molecule fragments; any molecules with inherent affinity for the pY binding site will preferentially form disulfides with the extender, allowing for their identification by mass spectrometry. The ability to start from a known substrate mimimizes perturbation of protein structure and increases the opportunity to probe the active site using tethering. We applied this approach to the anti-diabetic protein PTP1B to discover a pY mimetic which belongs to a new molecular class and which binds in a novel fashion. 相似文献
8.
In a combination of cobalt-mediated cationic and free radical chemistry, treatment of the allyl silane substituted β-hydroxycobaloxime 13 with pTSA led predominantly to the trans-disubstituted cyclopentane 14, which on irradiation with TEMPO produced 15. In a similar manner, the cobaloxime 18 was cyclised to 19 in the presence of pTSA which, on irradiation with a sunlamp then underwent radical mediated cyclisation to the substituted indane 20. 相似文献
9.
Jerald S. Bradshaw Krzysztof E. Krakowiak Reed M. Izatt Ronald L. Bruening Bryon J. Tarbet 《Journal of heterocyclic chemistry》1990,27(2):347-349
Two new dithia-crowns containing a hydroxy group and 1,4,7,10-tetrathia-18-crown-6 containing an allyl-oxymethyl substituent were prepared in good yields. Two of these crowns were covalently attached to silica gel. The silica gel-bound thia-crowns were used to separate gold( III ), palladium( II ), silver( I ) and mercury( II ) ions from an aqueous 0.1 M nitric acid solution which also contained 1.0 M ferric chloride. 相似文献
10.
L. H. Klemm Lee Lam Bryon Severns Sandip K. Sur 《Journal of heterocyclic chemistry》1990,27(7):1969-1972
Treatment of phenanthro[4,5-bcd]thiophene ( 2 ) with acetyl chloride and aluminum chloride in nitrobenzene gives acetylation of positions ortho and para to the heteroatomic sulfur atom. In separate experiments, mixtures of 1- and 3-acetyl (50% yield, ratio 1.9:1) or of 1,5-, 1,7-, and 3,5-diacetyl (79% yield, ratio 3:1:1) derivatives were obtained. Isolated as isomerically pure products were the 1-acetyl and the 1,5-diacetyl compounds, as well as the oximes of the 1- and 3-acetyl derivatives. Comparison of these results is made with those reported for nitration of 2 , which also occurs ortho and para to the sulfur atom, and with nitration and acetylation of pyrene (the benzolog of 2 ) which substitutes in the corresponding positions. 相似文献