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81.
The results of several approaches to make the 4,4,8-trimethyl-12-oxatricyclo[7.2.1.02,5]dodecane motif present in rumphellatins A–C are reported. The strategy adopted involved (9E)-12,12-dimethyl-5-oxatricyclo[8.2.0.04,6]dodec-9-en-11-ol as an intermediate, but when attempts were made to connect the third methyl group to the carbon skeleton by reacting the epoxide with MeLi under boron-trifluoride catalysis, an unprecedented transannular reaction occurred. The desired product was not formed; instead, compounds containing a tricyclo[6.3.0.02,5]undecane moiety were obtained, in one case in better than 70% yield. 相似文献
82.
Gangqiang Wang Sen Zhao Rongxing Chen Liangfeng Yang Jian Wang Haibing Guo Minghu Wu Justin Domena Yalan Xing Shaofa Sun 《Tetrahedron letters》2017,58(45):4308-4311
A highly efficient one-pot synthesis of thiazolidin-4-ones via [3+2] cycloaddition of aza-oxyallylic cations with isothiocyanates is developed. The aza-oxyallyic cations were generated in situ in the present of a base. This cycloaddition reaction allows the rapid access to a variety of thiazolidin-4-one derivatives in mild conditions, good yield, and excellent functional group compatibility. 相似文献
83.
Yun-Hua Wang 《Tetrahedron》2010,66(35):7136-6130
A simply performed procedure for the [Rh(cod)Cl]2/cationic 2,2′-bipyridyl system-catalyzed [2+2+2] cycloaddition of α,ω-diynes with terminal and internal alkynes was achieved in water under air at 60 °C. The reaction proceeded smoothly with 1 equiv α,ω-diynes and 3 equiv alkynes in the presence of 20 mol % KOH for 1 h or 9 h, resulting in the formation of tri- and tetra-substituted benzene derivatives in moderate to high yields. After separation of the organic products by extraction, the residual aqueous solution could be reused for further reactions until complete degradation of its catalytic activity. 相似文献
84.
A tricyclic core containing a 5,7-fused bicyclic unit of rameswaralide was prepared starting from a 1,6-enyne. The synthetic sequence involved (i) ruthenium-catalyzed [5+2]-cycloaddition of 1,6-enyne, (ii) an acyl radical based approach to construct the lactone, and (iii) a regioselective installation of the conjugated double bond by a concomitant sulfenylation-dehydrosulfenylation sequence. 相似文献
85.
Takenori Mitamura 《Tetrahedron letters》2010,51(27):3538-3194
Upon treatment of a mixture of alkynyl selenides and acetylenedicarboxylates with Pd(OAc)2/P(o-tol)3/K2CO3/H2O-catalytic system, the alkynylselenation of acetylenedicarboxylates takes place to give the corresponding alkynylvinyl selenides. Furthermore, alkynyl selenides undergo the intermolecular [2+2+2] cycloaddition reaction in the presence of PdCl2(PPh3)2 as a catalyst, affording the corresponding multisubstituted aryl selenides selectively. 相似文献
86.
Bis(tetraphenylphosphonium) hexachloridodiberyllate, (Ph4P)2[Be2Cl6], reacts with excess trimethylsilyl‐iso‐thiocyanate to give a mixture of colourless single crystals of (Ph4P)2[Be(NCS)4] ( 1 ) and (Ph4P)4[{Be2(NCS)4(μ‐NCS)2}{Be2(NCS)6(μ‐H2N2C2S2)}] ( 2 ), which can be separated by selection. Both complexes were characterized by X‐ray diffraction. Compound 1 can be prepared without by‐products by treatment of (Ph4P)2[BeCl4] with excess Me3SiNCS in dichloromethane solution. 1 : Space group I41/a, Z = 4, lattice dimensions at 100(2) K: a = b = 1091.2(1), c = 3937.1(3) pm, R1 = 0.0474. The [Be(NCS)4]2– ion of 1 forms tetragonally distorted tetrahedral anions with Be–N distances of 168.4(2) pm and weak intermolecular S ··· S contacts along [100] and [010]. 2 ·4CH2Cl2: Space group P , Z = 1, lattice dimensions at 100(2) K: a = 919.5(1), b = 1248.3(1), c = 2707.0(2) pm, α = 101.61(1) °, β = 95.08(1) °, γ = 94.52(1) °, R1 = 0.103. Compound 2 contains two different anionic complexes in the ratio 1:1. In {Be2(NCS)4(μ‐NCS)2}2–, the beryllium atoms are connected by (NCS)– bridging groups forming centrosymmetric eight‐membered Be2(NCS)2 rings with distances Be–N of 168(1) pm and Be–S of 235.2(9) pm. The second anion {Be2(NCS)6(μ‐H2N2C2S2)}2– consists of two {Be(NCS)3}– units, which are linked by the nitrogen atoms of the unique dimeric cyclo‐addition product of HNCS with Be–N distances of 179(1) pm. 相似文献
87.
Johannes ZagermannAnthony Deally Nils Metzler-NolteHelge Müller-Bunz Denise WallisMatthias Tacke 《Polyhedron》2011,30(14):2387-2390
An alkyne-substituted fulvene was transformed via hydridolithiation followed by transmetallation with titanium tetrachloride into bis-[p-(prop-2-ynyloxy)-benzyl-cyclopentadienyl] titanium(IV) dichloride. Single crystals of this titanocene derivative could be obtained and the structure determined by X-ray diffraction. It showed that this compound crystallises in the space group C2/c with four molecules in the monoclinic cell. The alkyne-substituted titanocene dichloride derivative was then subject to a copper-catalysed azide-alkyne cycloaddition with its azide-functionalised methylester-protected phenylalanine reaction partner in order to form a linking triazole. This reaction was performed under anhydrous conditions employing a dichloromethane/acetonitrile solvent mixture with copper(I) iodide and 2,6-lutidine as the catalyst system. Under these conditions the adduct between the protein mimic and the titanocene was formed without hydrolysing the titanium dichloride moiety. 相似文献
88.
N-Iodosaccharin (NISac): a new reusable catalyst for formal [2+4] cycloaddition of imines and enones
Ankita Rai 《Tetrahedron letters》2010,51(31):4045-3936
The first example of N-iodosaccharin (NISac)-catalyzed step, pot and atom economic synthesis of 1,3-oxazines via formal [2+4] cycloaddition of imines and enones has been reported. No by-product formation, operational simplicity, ambient temperature and high yields (85-95%) are the salient features of the present synthetic protocol. After isolation of the product, the catalyst NISac can be easily recovered and reused without any loss of efficiency. 相似文献
89.
Congde Huo Chougu SunDongcheng Hu Xiaodong JiaXiaolan Xu Zhongli Liu 《Tetrahedron letters》2011,52(51):7008-7010
The reaction of ethyl diazoacetate with aryl imines can be initiated by persistent cation radical salt tris(4-bromophenyl)aminium hexachloroantimonate, giving exclusively cis-aziridine carboxylates. 相似文献
90.