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1.
Benoít Rigo Etienne Tullier Didier Barbry Daniel Couturier Vincent Warin Jocelyne Lamiot Franois Baert 《Journal of heterocyclic chemistry》1990,27(5):1383-1386
3,5-Dihydrobenz[f]indolizin-3-one was prepared by a novel dehydration reaction involving the heating of 1,2,3,5,10,10a-hexahydro[f]indolizine-3,10-dione with polyphosphoric acid. The structure of this new compound was established by X-ray crystallography, by nmr spectroscopy and by reduction to the known products 1,2,3,5-tetrahydrobenz[f]indolizin-3-one and 1,2,3,5,10,10a-hexahydrobenz[f]indolizin-3-one. 相似文献
2.
Sanna D Micera G Kallay C Rigo V Sovago I 《Dalton transactions (Cambridge, England : 2003)》2004,(17):2702-2707
Copper(II) complexes of peptides containing two or three histidyl residues (Ac-HisGlyHis-OH, Ac-HisGlyHis-NHMe, Ac-HisHisGlyHis-OH and Ac-HisHisGlyHis-NHMe) have been studied by potentiometric, UV-Vis, EPR and CD spectroscopic measurements. The imidazole nitrogen atoms are described as the primary metal binding sites of all ligands resulting in the formation of various macrochelates in the pH range 4 to 7. The (Nim, N-, Nim)-co-ordinated [CuH-1L]0+ complexes were mainly detected in samples containing free carboxylates at the C-termini, whilst the [CuH-2L]-(0) complexes were the predominant species in slightly alkaline solution and their binding modes were described via 4N-co-ordination (Nim, N-, N-, Nim) in (7,5,6)-membered fused chelate rings. Deprotonation and co-ordination of the third amide nitrogens were detected above pH approximately 9 in all cases. 相似文献
3.
Cobalt(I) carbonyl complexes of formula [Co(CO)n(P)5?n]ClO4 (n = 1, 2, 3; P = secondary or tertiary phosphine) have been prepared by reaction of CO under ambient conditions with Co(ClO4)2 · 6H2O and phosphine in isopropyl alcohol. The chemical and spectroscopic properties of these complexes are described and the stoichiometry and mechanism of the carbonylation reaction discussed. 相似文献
4.
The synthesis and the characterization of cobalt(I) complexes of the type [Co(diene)(phosphine)3]Y (diene = 1,3-butadiene and isoprene; phosphine = PMe3, PMe2Ph, and HPPh2; Y = ClO4, BF4, or BPh4) are reported. The fluxional nature of the five-coordinate cations [Co(diene)(phosphine)3]+ is shown by variable-temperature NMR spectroscopy (1H and 31P). Low-temperature spectra are consistent with a square-pyramidal structure in which the diene occupies two basal coordination sites. 相似文献
5.
Dieter Seebach Paola E. Ciceri Mark Overhand Bernhard Jaun Dario Rigo Lukas Oberer Ulrich Hommel Ren Amstutz Hans Widmer 《Helvetica chimica acta》1996,79(8):2043-2066
Structural prerequisites for the stability of the 31 helix of β-peptides can be defined from inspection of models (Figs. 1 and 2): lateral non-H-substituents in 2- and 3-position on the 3-amino-acid residues of the helix are allowed, axial ones are forbidden. To be able to test this prediction, we synthesized a series of heptapeptide derivatives Boc-(β-HVal-β-HAla-β-HLeu-Xaa-β-HVal-β-HAla-β-HLeu)-OMe 13–22 (Xaa = α- or β-amino-acid residue) and a β-depsipeptide 25 with a central (S)-3-hydroxybutanoic-acid residue (Xaa = –OCH(Me)CH2C(O)–) (Schemes 1 3). Detailed NMR analysis (DQF-COSY, HSQC, HMBC, ROESY, and TOCSY experiments) in methanol solution of the β-hexapeptide H(-β-HVal-β-HAla-β-HLeu)2-OH ( 1 ) and of the β-heptapeptide H-β-HVal-β-HAla-β-HLeu-(S,S)-β-HAla(αMe)-β-HVal-β-HAla- β-HLeu-OH ( 22 ), with a central (2S,3S)-3-amino-2-methylbutanoic-acid residue, confirm the helical structure of such β-peptides (previously discovered in pyridine solution) (Fig.3 and Tables 1–5). The CD spectra of helical β-peptides, the residues of which were prepared by (retentive) Arndt-Eistert homologation of the (S)- or L -α-amino acids, show a trough at 215 nm. Thus, this characteristic pattern of the CD spectra was taken as an indicator for the presence of a helix in methanol solutions of compounds 13–22 and 25 (including partially and fully deprotected forms) (Figs.4–6). The results fully confirm predicted structural effects: incorporation of a single ‘wrong’ residue ((R)-β-HAla, β-HAib, (R,S)-β-HAla(α Me), or N-Me-β-HAla) in the central position of the β-heptapeptide derivatives A (see 17, 18, 20 , or 21 , resp.) causes the CD minimum to disappear. Also, the β-heptadepsipetide 25 (missing H-bond) and the β-heptapeptide analogs with a single α-amino-acid moiety in the middle ( 13 and 14 ) are not helical, according to this analysis. An interesting case is the heptapeptide 15 with the central achiral, unsubstituted 3-aminopropanoic-acid moiety: helical conformation appears to depend upon the presence or absence of terminal protection and upon the solvent (MeOH vs. MeOH/H2O). 相似文献
6.
We have studied the reduction of SeIV in acidic medium (1 M HCl and 1 M HClO4) by classical and alternating current polarography and single sweep linear voltammetry with dropping mercury electrode and hanging mercury drop (HMDE). Two steps are observed distinctly: (1) The reduction of SeIV→Seo leads to a deposit of adsorbed elementary selenium. A mathematical expression is shown for the variation of current which is related to the surface covered at the HMDE. (2) The second step is the reduction of Seo→Se2? which takes place at more negative potentials. The accumulation of Seo may be used for the determination of traces in trace analysis by cathodic stripping. It appears that the behavior of selenium in these two mineral acids is similar. But sometimes it behaves in a different manner, especially in a.c. polarography (in this connection the influence of frequency and demodulation angle are important). 相似文献
7.
Christian Miquel Pierre Pigache Benoit Rigo Nicolas Kolocouris 《Journal of heterocyclic chemistry》1980,17(7):1447-1453
Starting from the readily available 5-oxo-2-carboxypyrrolidine, methylene-bis-(N-5-oxo-2-carboxypyrrolidine) was prepared and transformed into a diamine, then into two isomeric diols, which cyclised into one ether. The meso configuration has been assigned for this ether. The reduction of both diols and ether was complete and gave rise to methylene-bis-N-pyrrolidine. 相似文献
8.
Dr. Massimo Rigo Evi R. M. Habraken Dr. Koyel Bhattacharyya Manuela Weber Dr. Andreas W. Ehlers Dr. Nicolas Mézailles Dr. J. Chris Slootweg Prof. Dr. Christian Müller 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(37):8769-8779
A series of substituted phosphinines, 1-phosphabarrelenes and 5-phosphasemibullvalenes were synthesized and evaluated for their potential application as ligands in homogeneous catalytic reactions. While their buried volume (%Vbur) was calculated to get insight into the steric properties, [LNi(CO)3] complexes were prepared in order to determine the corresponding Tolman electronic parameter. ETS-NOCV (extended-transition-state natural orbital for chemical valence) calculations on [LAuCl] complexes further allowed an estimation of the σ- and π-contributions to the L− M interaction. AuI coordination compounds of selected examples were prepared and characterized by single crystal X-ray diffraction. Finally, the three classes of PIII compounds were successfully used in the AuI-catalyzed cycloisomerization of N-2-propyn-1-ylbenzamide, showing very good activities and selectivities, which are comparable with the reported data of cationic phosphorus-based gold catalysts. 相似文献
9.
Fanny Danton Dr. Mohamed Othman Dr. Ata Martin Lawson Dr. Ján Moncol Dr. Alina Ghinet Prof. Benoît Rigo Prof. Adam Daïch 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(24):6113-6118
An efficient domino transformation using a phenyliodine(III) diacetate (PIDA)/I2 combination towards Morin 1,4-thiazine compounds has been developed starting from N,S-acetals. The latter leads to “one-step” regioselective methylene insertion without the need for traditional sulfoxide intermediates in good yields. The reaction involves easily accessible N,S-acetals obtained from cost-effective basic ketones and cysteamine as starting materials. This process ultimately leads to 1,4-thiazines related to natural product and fused derivatives necessary for further QSAR study. 相似文献
10.
Benoit Rigo Philippe Gautret Anne Legrand Samira El Ghammarti Daniel Couturier 《合成通讯》2013,43(18):2609-2615
Starting from the readily available N,O-bis trimethylsilyl pyroglutamate, an easy high yield one pot synthesis of ketone 1 was described. 相似文献