Assembly of organosilver(I) frameworks with terminal ethynide and ethenyl groups on separate pendent arms attached to an aromatic ring
摘要:
A series of eight silver(I) trifluoroacetate complexes based on aromatic ligands bearing terminal ethynyl and ethenyl groups on separate pendent arms has been synthesized. Single-crystal X-ray analysis of the complexes provided detailed information on the influence of argentophilicity, ligand disposition and orientation, and the co-existence of three types of silver-carbon bonding (silver-ethynide, silver-ethenyl and silver-aromatic) in coordination network construction, as well as the roles played by weak pi-pi stacking and anion-pi interactions in supramolecular assembly. (C) 2012 Elsevier Ltd. All rights reserved.
Metal-Free Sequential C(sp<sup>2</sup>)–H/OH and C(sp<sup>3</sup>)–H Aminations of Nitrosoarenes and <i>N</i>-Heterocycles to Ring-Fused Imidazoles
作者:Anisha Purkait、Subhra Kanti Roy、Hemant Kumar Srivastava、Chandan K. Jana
DOI:10.1021/acs.orglett.7b00832
日期:2017.5.19
Hydrogen bond assisted ortho-selective C(sp2)–Hamination of nitrosoarenes and subsequent α-C(sp3)-H functionalization of aliphatic amines is achieved under metal-free conditions. The annulation of nitrosoarenes and 2-hydroxy-C-nitroso compounds with N-heterocycles provides a facile excess to a wide range of biologically relevant ring-fused benzimidazoles and structurally novel polycyclic imidazoles
氢键辅助的亚硝基芳烃的邻位选择性C(sp 2)-H氨基化和随后的α-C(sp 3)-H脂肪族胺的官能化在无金属条件下实现。亚硝基芳烃和2-羟基-C-亚硝基化合物与N-杂环的环化分别提供了相对于广泛的生物学相关的环稠合的苯并咪唑和结构上新颖的多环咪唑的简便过量。发现在卤代亚硝基芳烃的C(sp 2)–H胺化过程中,亲核芳香族氢取代(S N ArH)比经典S N Ar反应更可取。
Synthesis, Resolution, and Absolute Configuration of Chiral Tris(2-pyridylmethyl)amine-Based Hemicryptophane Molecular Cages
racemic mixture of each hemicryptophane host can be readily resolved by chiral HPLC, giving an easy access to the enantiopure molecular cages of which absoluteconfigurations have been assigned by ECD spectroscopy. These new hemicryptophanes are available chemical platforms ready to use for various purposes due to the versatile metal complexation properties of the TPA unit. A Zn(II)@hemicryptophane
Organocatalytic Friedel-Crafts Alkylation/Lactonization Reaction of Naphthols with 3-Trifluoroethylidene Oxindoles: The Asymmetric Synthesis of Dihydrocoumarins
Naphthols and 3‐trifluoroethylidene oxindoles were found to undergo an asymmetric Friedel–Crafts alkylation/lactonization reaction, catalyzed by only 2.5 mol % of a quinine‐derived squaramide catalyst, to afford the corresponding α‐aryl‐β‐trifluoromethyl dihydrocoumarin derivatives in high yields (up to 99 %) with excellent enantio‐ and diastereoselectivities (up to 98 % ee, >20:1 d.r.). Importantly
The present invention provides an oxazine compound which contains a group having an aromatic ring structure and a plurality of specified carbon-carbon double bond structure so as to achieve an object. The present invention further provides a composition containing the oxazine compound of the present invention, a cured product containing the composition, and a laminate having a layer of the cured product. The present invention further still provides a composition for a heat-resistant material and a composition for an electronic material, which contain the composition containing the oxazine compound of the present invention so as to achieve the object.
The present invention provides an oxazine compound which contains a group having an aromatic ring structure and a plurality of specified carbon-carbon double bond structure so as to achieve an object. The present invention further provides a composition containing the oxazine compound of the present invention, a cured product containing the composition, and a laminate having the cured product layer. The present invention further still provides a composition for a heat-resistant material and a composition for an electronic material, which contain the composition containing the oxazine compound of the present invention so as to achieve an object.