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排序方式: 共有109条查询结果,搜索用时 15 毫秒
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Bapurao B. Shingate Vandana S. Pore Rajesh G. Gonnade Mohan M. Bhadbhade 《Tetrahedron》2007,63(25):5622-5635
A stereoselective total synthesis of naturally occurring 20-epi cholanic acid derivatives has been realized, starting from readily available 16-dehydropregnenolone acetate. The key step of these syntheses involves an ionic hydrogenation of a C-20,22-ketene dithioacetal and deoxygenation of steroidal C-20 tert-alcohols, to set up the unnatural C(20R) configuration with 100% stereoselectivity. The unnatural C-22 aldehydes with C(20R) stereocenters thus obtained were elaborated to 20-epi cholanic acid derivatives. Two derivatives of 20-epi cholanic acid were synthesized and their structures have been confirmed by single crystal X-ray analysis. Catalytic hydrogenation of 16-dehydropregnenolone acetate and 16-dehydropregnenolone in ethanol affords C-5,C-16 tetrahydro products. Crystal structure analysis of one of these products revealed C-5α and C-17α configurations of the hydrogen atoms. 相似文献
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Siddiqui Madiha M. Nagargoje Amol A. Akolkar Satish V. Sangshetti Jaiprakash N. Khedkar Vijay M. Pisal Parshuram M. Shingate Bapurao B. 《Research on Chemical Intermediates》2022,48(3):1199-1225
Research on Chemical Intermediates - A simple and efficient protocol has been developed for the synthesis of new1,2,3-triazole-2,3-dihydroquinazolin-4[1H]-one (DHQ) conjugates(6a?j) via... 相似文献
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A. Sengupta B. Rajeswari R. M. Kadam R. J. Kshirsagar 《Journal of Radioanalytical and Nuclear Chemistry》2012,292(2):903-908
The use of serpentine as a potential nuclear shielding material necessitates a chemical quality control of the samples before
its use in reactors. With this in view, characterization of these mineral samples was carried out using inductively coupled
plasma atomic emission spectrometry (ICP-AES) and Instrumental neutron activation analysis (INAA) methods. The analytical
results obtained by both ICP-AES and NAA techniques were found to be comparable. Na, Cr, Co, Zn, and Cu were found to be present
in all samples of Indian origin while Ga, Ag, Ni, and Cd were found to below the limits of detection. A comparison on the
detection limits of elements of interest was also carried out by both the analytical techniques and found to be in good agreement.
An infrared spectroscopic investigation was also carried out on all the mineral samples. Bands at 3,689 and 3,648 cm−1 were attributed to inner and outer hydroxyl stretching of Mg–OH, respectively. The weak and broad band centered around 3,416 cm−1 was assigned due to the stretching vibrations of the adsorbed water molecules while three bands at 1076, 1022 and 968 cm−1 were prescribed to the vibrations of the SiO4 tetrahedra. 相似文献
6.
Kirti S. Niralwad Bapurao B. Shingate Murlidhar S. Shingare 《Ultrasonics sonochemistry》2010,17(5):760-763
1-Hexanesulphonic acid sodium salt was found to be an efficient catalyst for the green synthesis of α-aminophosphonates by the coupling of aldehydes/ketone, an amine and triethyl phosphite under ultrasound irradiation at ambient temperature for appropriate time to furnish the desired product in good to excellent yield under solvent-free condition. This catalyst provides clean conversion; greater selectivity and easy workup make this protocol practical and economically attractive. 相似文献
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Shreyans K. Jain Samdarshi Meena Asif K. Qazi Aashiq Hussain Sunil K. Bhola Rajendra Kshirsagar Koteppa Pari Anamika Khajuria Abid Hamid R. Uma Shaanker Sandip B. Bharate Ram A. Vishwakarma 《Tetrahedron letters》2013
The chromone alkaloid dysoline (1), a new regioisomer of rohitukine (2) along with rohitukine and rohitukine-N-oxide (3) were isolated from the stem barks of Dysoxylum binectariferum. The structure of dysoline (1) was determined by extensive 2D-NMR studies and the absolute configuration was established by NOESY and CD spectra. Dysoline (1) consisted of a 5,7-dihydroxy-2-methylchromone nucleus substituted with a 2′-hydroxylated N-Me piperidine ring at the C-6 position. Dysoline differs from rohitukine by the position of the piperidine ring on the chromone nucleus. Dysoline displayed promising cytotoxicity in HT1080 fibrosarcoma cells with an IC50 of 0.21 μM, and also displayed significant inhibition of proinflammatory cytokines TNF-α and IL-6. 相似文献
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Dr. Umesh A. Kshirsagar Regev Parnes Hagit Goldshtein Dr. Rivka Ofir Dr. Raz Zarivach Dr. Doron Pappo 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(40):13575-13583
An iron‐based cross‐dehydrogenative coupling (CDC) approach was applied for the diversity‐oriented synthesis of coumestrol‐based selective estrogen receptor modulators (SERMs), representing the first application of CDC chemistry in natural product synthesis. The first stage of the two‐step synthesis of coumestrol involved a modified aerobic oxidative cross‐coupling between ethyl 2‐(2,4‐dimethoxybenzoyl)acetate and 3‐methoxyphenol, with FeCl3 (10 mol %) as the catalyst. The benzofuran coupling product was then subjected to sequential deprotection and lactonization steps, affording the natural product in 59 % overall yield. Based on this new methodology other coumestrol analogues were prepared, and their effects on the proliferation of the estrogen receptor (ER)‐dependent MCF‐7 and of the ER‐independent MDA‐MB‐231 breast cancer cells were tested. As a result, new types of estrogen receptor ligands having an acetamide group instead of the 9‐hydroxyl group of coumestrol were discovered. Both 9‐acetamido‐coumestrol and 8‐acetamidocoumestrol were found more active than the natural product against estrogen‐dependent MCF‐7 breast cancer cells, with IC50 values of 30 and 9 nM , respectively. 相似文献
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Rhodium Enalcarbenoids: Direct Synthesis of Indoles by Rhodium(II)‐Catalyzed [4+2] Benzannulation of Pyrroles
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Sudam Ganpat Dawande Vinaykumar Kanchupalli Jagadeesh Kalepu Haribabu Chennamsetti Bapurao Sudam Lad Dr. Sreenivas Katukojvala 《Angewandte Chemie (International ed. in English)》2014,53(16):4076-4080
Disclosed herein is the design of an unprecedented electrophilic rhodium enalcarbenoid which results from rhodium(II)‐catalyzed decomposition of a new class of enaldiazo compounds. The synthetic utility of these enalcarbenoids has been successfully demonstrated in the first transition‐metal‐catalyzed [4+2] benzannulation of pyrroles, thus leading to substituted indoles. The new benzannulation has been applied to the efficient synthesis of the natural product leiocarpone as well as a potent adipocyte fatty‐acid binding protein inhibitor. 相似文献