排序方式: 共有58条查询结果,搜索用时 0 毫秒
1.
[reaction: see text] A broad range of substituted 1-amino-1,3-butadienes undergo enantioselective Diels-Alder reactions with methacrolein in the presence of 5 mol % of Cr(III)-salen complex 1. The reactions are carried out conveniently, at room temperature, and they afford the cycloadducts in high yields and excellent ee's. 相似文献
2.
An efficient, convergent synthesis of the core bicyclo[4.3.1]decane ring system of welwitindolinones is described. Key steps in the synthesis include an intramolecular palladium-catalyzed enolate arylation reaction to create the desired bicyclic skeleton and a Curtius rearrangement to install the bridgehead isocyanate unit. [reaction: see text] 相似文献
3.
The toughness of a (noncomplete) graph G is the minimum value of t for which there is a vertex cut A whose removal yields components. Determining toughness is an NP‐hard problem for general input graphs. The toughness conjecture of Chvátal, which states that there exists a constant t such that every graph on at least three vertices with toughness at least t is hamiltonian, is still open for general graphs. We extend some known toughness results for split graphs to the more general class of 2K2‐free graphs, that is, graphs that do not contain two vertex‐disjoint edges as an induced subgraph. We prove that the problem of determining toughness is polynomially solvable and that Chvátal's toughness conjecture is true for 2K2‐free graphs. 相似文献
4.
Magnus Bordewich Catherine Greenhill Viresh Patel 《Random Structures and Algorithms》2016,48(1):21-52
We present several results on the mixing time of the Glauber dynamics for sampling from the Gibbs distribution in the ferromagnetic Potts model. At a fixed temperature and interaction strength, we study the interplay between the maximum degree (Δ) of the underlying graph and the number of colours or spins (q) in determining whether the dynamics mixes rapidly or not. We find a lower bound L on the number of colours such that Glauber dynamics is rapidly mixing if at least L colours are used. We give a closely‐matching upper bound U on the number of colours such that with probability that tends to 1, the Glauber dynamics mixes slowly on random Δ‐regular graphs when at most U colours are used. We show that our bounds can be improved if we restrict attention to certain types of graphs of maximum degree Δ, e.g. toroidal grids for Δ = 4. © 2014 Wiley Periodicals, Inc. Random Struct. Alg., 48, 21–52, 2016 相似文献
5.
As part of a comprehensive strategy to the welwitindolinone alkaloids possessing a bicyclo[4.3.1]decane core, we report herein concise asymmetric total syntheses of (-)-N-methylwelwitindolinone C isothiocyanate (2a), (-)-N-methylwelwitindolinone C isonitrile (2b), and (-)-3-hydroxy-N-methylwelwitindolinone C isothiocyanate (3a) from a common tetracyclic intermediate. The crucial vinyl chloride moiety was installed through electrophilic chlorination of a hydrazone, but only after adjustment of reactivity to circumvent a facile skeletal rearrangement. Selective desulfurization and oxidation of 2a provided access to 2b and 3a, respectively. Notably, this work provides corrected (1)H and (13)C NMR spectral data for 3a. 相似文献
6.
A general method for regioselective C3-benzylation of indoles has been developed. Various 3-substituted indoles and benzyl methyl carbonates with different electronic properties react under mild conditions to afford a diverse range of 3-benzylindolenine products in good yields. 相似文献
7.
8.
Julius R. Reyes Prof. Dr. Viresh H. Rawal 《Angewandte Chemie (International ed. in English)》2016,55(9):3077-3080
A method is presented for the direct transformation of a ketone to the corresponding reduced alkyl chloride or bromide. The process involves the reaction of a ketone trityl hydrazone with tBuOCl to give a diazene which readily collapses to the α‐chlorocarbinyl radical, reduction of which by a hydrogen atom source gives the alkyl chloride product. The use of N‐bromosuccinimide provides the corresponding alkyl bromide. This unique transformation provides a reductive halogenation that complements Barton's redox‐neutral vinyl halide synthesis. 相似文献
9.
The t-Butyloxycarbonyl (BOC) group on indoles and pyrroles can be removed cleanly and in high yield by simple thermolysis: no acid, no base, no solvent is required. 相似文献
10.
Inter- and intramolecular arylations of trimethylsilyl enol ethers with aryl halides are accomplished regiospecifically in the presence of a palladium catalyst and tributyltin fluoride in refluxing benzene or toluene. The optimal catalyst system called for the use of Pd2(dba)3 and tri-tert-butylphosphine in ca. 1:2 ratio. Aryl iodides, bromides, and chlorides are all effective arylation partners in this reaction. [reaction: see text] 相似文献