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991.
992.
Ohne Zusammenfassung 相似文献
993.
Summary The paper deals with the convergence ofR. Grammel's method for the solution of boundary-eigenvalue-problems. It is further shown thatGrammel's method can be extended to the case where it is difficult to find the exactGreen function. In this case one may use a different, relatedGreen function if one adds certain supplemental terms to the properGrammel equations. 相似文献
994.
Horst Leptin 《Mathematische Annalen》1958,135(4):360-368
Ohne Zusammenfassung 相似文献
995.
While a solution of TpPh,MeZn-OH in methanol contains only traces of TpPh,MeZn-OMe, according to the equilibrium constant K = 5.8 x 10(-4), the reactions of TpPh,MeZn-OH with the electronegative alcohols trifluoroethanol and hexafluoro-2-propanol easily yield TpPh,MeZn-OCH2CF3 and TpPh,MeZn-OCH(CF3)2. The extremely hydrolytically sensitive TpPh,MeZn-OR complexes, with R = Me, Et, i-Pr, and CH2CH2F, as well as TpCum,MeZn-OR, with R = Me and i-Pr, are accessible from the Tp*Zn-hydride complexes and the corresponding alcohol. Alkylations with methyl iodide have revealed the high nucleophilicity of TpPh,MeZn-OMe by conversion to dimethyl ether and TpPh,MeZn-I. This conversion occurs rapidly not only with pure TpPh,MeZn-OMe but also with TpPh,MeZn-OH (as such or in the presence of methanol) and with TpPh,MeZn-OCOOMe. A relation of the Tp*Zn-alkoxides to the function of the zinc enzyme alcoholdehydrogenase exists in the reaction of TpPh,MeZn-OCH(CH3)2 with aromatic aldehydes, which yields acetone and the corresponding benzyl oxides TpPh,MeZn-OH2Ar. The heterocumulenes carbon dioxide, carbon disulfide, isothiocyanates, and one isocyanate are inserted into the Zn-OR bonds, yielding one alkyl carbonate complex (TpPh,MeZn-OC(O)OMe), two xanthogenate complexes (TpPh,MeZn-SC(S)OR), three iminothiocarbonate complexes (TpPh,MeZn-SC(NR')OR), and one alkyl carbamate complex (TpPh,MeZn-NR-COOMe). All insertion reactions can be described by a common mechanism involving a four-center intermediate in which the most basic heteroatom of the heterocumulene is attached to zinc. 相似文献
996.
A 2,3,4-tri-O-pivaloylated beta-D-galactopyranosyl azide bearing a hydroxy-functionalized spacer unit at the C-6 position of the galactose was synthesized and immobilized on the solid phase by using a polymer-bound chlorosilane. The azide was reduced to the corresponding galactopyranosylamine, which served as a versatile chiral auxiliary in highly diastereoselective Ugi four-component condensation reactions at ambient temperature. Fluoride-induced cleavage from the polymeric support furnished N-glycosylated N-acylated alpha-amino acid amides. The reaction of the immobilized galactosylamine with aldehydes gave rise to the corresponding aldimines, which underwent a domino Mannich-Michael condensation reaction with Danishefsky's diene at ambient temperature to yield 2-substituted 5,6-didehydropiperidin-4-ones on the solid phase. Subsequent cleavage with tetra-n-butylammonium fluoride delivered the N-glycosylated products in high yields, purities, and diastereoselectivities. A chemoselective 1,4-hydride addition to the polymer-bound dehydropiperidinones was achieved in the presence of the bulky oxygenophilic Lewis acid methylaluminum [bis(2,6-di-tert-butyl-4-methylphenoxide)]. The conjugate addition of cyano-modified Gilman reagents to the immobilized dehydropiperidinones furnished 2,6-cis-substituted piperidine derivatives as the major diastereomers that were isolated after cleavage from the support. 相似文献
997.
The trigonometric sum
998.
Rühl T Volke D Stembera K Hatanaka Y Hennig H Schumer F Welzel P 《Chemical communications (Cambridge, England)》2002,(15):1630-1631
The photolytic decomposition of trifunctional carbene generating photoaffinity probes in methanolic solution was studied, a cleavage reaction with butylamine in water, the conjugation with a ligand (moenomycin), and experiments that demonstrate that the fully armed probes interact with penicillin-binding protein 1b. 相似文献
999.
Aime S Barge A Batsanov AS Botta M Castelli DD Fedeli F Mortillaro A Parker D Puschmann H 《Chemical communications (Cambridge, England)》2002,(10):1120-1121
The rate of axial water exchange in well-defined series of lanthanide complexes depends on the extent of second sphere hydration which is determined by complex hydrophobicity and the nature of the lanthanide ion and its counter-ion. 相似文献
1000.