全文获取类型
收费全文 | 167篇 |
免费 | 17篇 |
国内免费 | 3篇 |
专业分类
化学 | 187篇 |
出版年
2023年 | 2篇 |
2022年 | 1篇 |
2021年 | 3篇 |
2020年 | 5篇 |
2019年 | 1篇 |
2018年 | 7篇 |
2017年 | 1篇 |
2016年 | 4篇 |
2015年 | 4篇 |
2014年 | 8篇 |
2013年 | 19篇 |
2012年 | 8篇 |
2011年 | 11篇 |
2010年 | 4篇 |
2009年 | 10篇 |
2008年 | 9篇 |
2007年 | 15篇 |
2006年 | 11篇 |
2005年 | 13篇 |
2004年 | 14篇 |
2003年 | 10篇 |
2002年 | 6篇 |
2001年 | 4篇 |
2000年 | 4篇 |
1999年 | 3篇 |
1998年 | 1篇 |
1997年 | 3篇 |
1996年 | 2篇 |
1994年 | 2篇 |
1988年 | 1篇 |
1984年 | 1篇 |
排序方式: 共有187条查询结果,搜索用时 437 毫秒
51.
Synthesis of N-tosylimines of arylaldehydes was carried out by the reaction of arylaldehydes and p-toluenesulfonamide in methylene chloride in the presence of trifluoroacetic anhydride as a dehydrating agent. 相似文献
52.
The alkylation of 2-(diphenylphosphino)-3-pyrrolidin-1-ylbut-2-enenitrile with a set of bromoacetophenones has been studied. Cyclization of the phosphonium salts into 6-cyano-3-hydroxy-3-aryl-1,1-diphenyl-5-pyrrolidin-1-yl-1,2,3,4-tetrahydrophosphininium bromides under heating in the presence of catalytic amount of a base is discussed. Starting both from the acyclic and the cyclic phosphonium salts, new types of λ5-phosphinines have been synthesized. 相似文献
53.
Vasil"ev L. S. Sheremetev A. B. Khoa N. K. Dem"yanets Z. K. Dmitriev D. E. Dorokhov V. A. 《Russian Chemical Bulletin》2001,50(7):1280-1286
In the presence of nickel acetylacetonate, -dicarbonyl compounds readily add at the nitrile group of 4-R-3-cyanofurazans to form enaminofurazans. The adducts obtained from 4-amino-3-cyanofurazan underwent intramolecular cyclization on heating with AcOH in EtOH to give furazano[3,4-b]pyridine derivatives in high yields. 相似文献
54.
55.
56.
Jasper S. Möhler Dr. Tobias Schnitzer Prof. Helma Wennemers 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(67):15623-15628
Stereoselective organocatalytic C−C bond formations that tolerate N-heterocycles are valuable since these moieties are common motifs in numerous chiral bioactive compounds. Such transformations are, however, challenging since N-heterocyclic moieties can interfere with the catalytic reaction. Here, we present a peptide that catalyzes conjugate addition reactions between aldehydes and nitroolefins bearing a broad range of different N-heterocyclic moieties with basic and/or H-bonding sites in excellent yields and stereoselectivities. Tuning of the pyramidalization direction of the enamine intermediate enabled the high stereoselectivity. 相似文献
57.
58.
Heating 5,13-dihydro-11H-isoquino[3,2-b]quinazolin-11-one with isonicotinoyl chloride in pyridine gives 6-isonicotinoyl-5,13-dihydro-11H-isoquino[3,2-b]quinazolin-11-one. The 1-alkyl-4[(11-oxo-5,13-dihydro-11H-isoquino[3,2-b]quinazolin-6-yl)carbonyl]pyridinium iodides obtained by alkylation of 6-isonicotinoyl-5,13-dihydro-11H-isoquino[3,2-b]quinazolin-11-one using alkyl iodides in the presence of NaH are converted to 1′-R-spiro[7H,8H-2a,7a-diazacyclopenta[fg]naphthacene-2,4′(1′H)-pyridine]-1,8(2H)-diones. The chemical and spectroscopic properties of the spiro compounds obtained
were studied.
For Communication 32 see [1].
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 52–58, January, 2009. 相似文献
59.
60.
A. N. Vasiliev Ya. S. Kayukov A. N. Lyshchikov O. E. Nasakin O. V. Kayukova 《Chemistry of Heterocyclic Compounds》2003,39(9):1182-1187
The reaction of alkyl 5,6-dialkyl-2-amino-3-cyano-4-pyridinecarboxylates with certain O-nucleophiles was investigated, as a result of which 6,7-dialkyl-4-amino-2,3-dihydro-1H-pyrrolo[3,4-c]pyridine-1,3-diones were synthesized. 相似文献