全文获取类型
收费全文 | 95篇 |
免费 | 3篇 |
专业分类
化学 | 51篇 |
晶体学 | 7篇 |
力学 | 11篇 |
数学 | 13篇 |
物理学 | 16篇 |
出版年
2022年 | 1篇 |
2021年 | 4篇 |
2019年 | 3篇 |
2017年 | 4篇 |
2016年 | 2篇 |
2014年 | 6篇 |
2013年 | 10篇 |
2012年 | 5篇 |
2011年 | 11篇 |
2010年 | 5篇 |
2009年 | 4篇 |
2008年 | 5篇 |
2007年 | 5篇 |
2006年 | 9篇 |
2005年 | 2篇 |
2004年 | 1篇 |
2003年 | 4篇 |
2002年 | 1篇 |
2001年 | 2篇 |
2000年 | 2篇 |
1998年 | 1篇 |
1997年 | 1篇 |
1995年 | 1篇 |
1994年 | 2篇 |
1993年 | 1篇 |
1992年 | 2篇 |
1990年 | 1篇 |
1989年 | 1篇 |
1987年 | 1篇 |
1985年 | 1篇 |
排序方式: 共有98条查询结果,搜索用时 15 毫秒
1.
A new solid-phase synthesis of trisubstituted 6-amino-2,4-dioxo-3,4-dihydro-1,3,5-triazines from a resin-bound amine component is described. The amine was readily converted to the corresponding polymer-bound S-methylthiopseudourea, which upon reaction with secondary amines gave the disubstituted guanidines. Cyclization of the polymer-bound guanidines with chlorocarbonylisocyanate afforded the triazinediones. The third point of diversity was introduced by the Mitsunobu reaction. The method is amenable for iterative combinatorial library generation. 相似文献
2.
On the construction of periodic solutions of kaplan-yorke type for some differential delay equations
In this paper we point out the main idea to yield periodic solutions of Kaplan-Yorke type of differential delay equations. Some new sufficient conditions for the existence of Kaplan-Yorke type periodic solutions have been given. Many interesting examples are also disscused. 相似文献
3.
M. Gopalakrishnan P. Sureshkumar V. Kanagarajan J. Thanusu Shanmugam Govindan Mahesh Reddy Ghanta 《合成通讯》2013,43(13):1923-1926
The p‐toluenesulphonic acid–catalyzed reaction between appropriate cresols and N‐methyl‐3‐phenyl‐3‐hydroxypropylamine in refluxing toluene resulted in the formation of o‐substituted phenol derivatives by an aromatic nucleophilic substitution reaction. 相似文献
4.
5.
Cover Picture: Direct Catalytic Addition of Alkylnitriles to Aldehydes by Transition‐Metal/NHC Complexes (Chem. Eur. J. 48/2014)
下载免费PDF全文
![点击此处可从《Chemistry (Weinheim an der Bergstrasse, Germany)》网站下载免费的PDF全文](/ch/ext_images/free.gif)
6.
7.
8.
K. Gopalsamy M. R. S. Kulenović G. Ladas 《Journal of Dynamics and Differential Equations》1990,2(2):117-132
LetP(t) denote the density of mature cells in blood circulation. Mackey and Glass (1977) have proposed the following equations:
相似文献
9.
Shaikh AY Sureshkumar G Pati D Sen Gupta S Hotha S 《Organic & biomolecular chemistry》2011,9(17):5951-5959
Propargyl 1,2-O-orthoesters are exploited for the synthesis of 1,2-trans O-glycosides of protected amino acids. N-Fmoc- and N-Cbz protected serine/threonine - benzyl/methyl esters reacted well with glucosyl-, galactosyl-, mannosyl- and lactosyl- derived propargyl 1,2-orthoesters affording respective 1,2-trans glycosides in good yields under AuBr(3)/4 ? MS Powder/CH(2)Cl(2)/rt. t-Boc serine derivative gave serine 1,2-orthoester and glycosyl carbamate. Optimized conditions enabled preparation of new glycosyl carbamates from N-Boc protected amines in a single step using gold catalysts and propargyl 1,2-orthoesters in excellent yields. 相似文献
10.
Iwata M Yazaki R Chen IH Sureshkumar D Kumagai N Shibasaki M 《Journal of the American Chemical Society》2011,133(14):5554-5560
A direct catalytic asymmetric aldol reaction of thioamides using a soft Lewis acid/hard Br?nsted base cooperative catalyst comprising (R,R)-Ph-BPE/[Cu(CH(3)CN)(4)]PF(6)/LiOAr is described. Exclusive enolate generation from thioacetamides through a soft-soft interaction with the soft Lewis acid allowed for a direct aldol reaction to α-nonbranched aliphatic aldehydes, which are usually susceptible to self-condensation under conventional basic conditions. A hard Lewis basic phosphine oxide has emerged as an effective additive to constitute a highly active ternary soft Lewis acid/hard Br?nsted base/hard Lewis base cooperative catalyst, enabling a direct enantio- and diastereoselective aldol reaction of thiopropionamides. Strict control of the amount of the hard Lewis base was essential to drive the catalytic cycle efficiently with a minimized retro-aldol pathway, affording syn-aldol products with high stereoselectivity. Divergent transformation of the thioamide functionality is an obvious merit of the present aldol methodology, allowing for a facile transformation of the aldol product into the corresponding aldehyde, ketone, amide, amine, and ketoester. An aldehyde derived from the direct aldol reaction was subjected to a second direct aldol reaction, which proceeded in a catalyst-controlled manner to provide 1,3-diols with high stereoselectivity. 相似文献
|