1370710-14-7Relevant academic research and scientific papers
Transition Metal-Free Synthesis of 3-Alkynylpyrrole-2-carboxylates via Michael Addition/Intramolecular Cyclodehydration
Teng, Qing-Hu,Xu, Yan-Li,Liang, Ying,Wang, Heng-Shan,Wang, Ying-Chun,Pan, Ying-Ming
, p. 1897 - 1902 (2016)
A transition metal-free and efficient method for the synthesis of 3-alkynylpyrrole-2-carboxylates from diynones and glycine esters or 2-aminoacetophenone hydrochloride has been developed. This transformation provides a large range of substituted pyrroles in good to excellent yields with the elimination of water as the only by-product. The detailed mechanistic studies elucidated that this transformation involves a Michael addition/intramolecular cyclodehydration process. (Figure presented.) .
An Unexpected Domino Reaction of β-Keto Sulfones with Acetylene Ketones Promoted by Base: Facile Synthesis of 3(2H)-Furanones and Sulfonylbenzenes
Tong, Wei,Li, Qian-Yu,Xu, Yan-Li,Wang, Heng-Shan,Chen, Yan-Yan,Pan, Ying-Ming
supporting information, p. 4025 - 4035 (2017/11/21)
An unexpected domino reaction of β-keto sulfones with acetylene ketones has been developed. The domino reaction of β-keto sulfones with diynones proceeded smoothly in the presence of 30 mol% K2CO3 without other additives, and afforded the novel 3(2H)-furanone derivatives. On replacing the diynones with terminal alkyne ketones, the reaction regioselectivity was changed and sulfonylbenzenes were obtained via benzannulation in good yields. (Figure presented.).
Effects of dendronization on the linear and third-order nonlinear optical properties of bis(thiopyrylium) polymethine dyes in solution and the solid state
Scarpaci, Annabelle,Nantalaksakul, Arpornrat,Hales, Joel M.,Matichak, Jonathan D.,Barlow, Stephen,Rumi, Mariacristina,Perry, Joseph W.,Marder, Seth R.
scheme or table, p. 1606 - 1618 (2012/08/13)
Effects of the size and attachment position of benzyl aryl ether dendrons covalently attached to bis(thiopyrylium) penta- and heptamethines on the optical properties of these dyes in solution and in solid films have been investigated. In dilute solution the low-energy absorption bands of some of the dendronized species differ from those of the parent compounds in having much smaller transition dipole moments, this effect possibly due to differences in ion pairing, while at higher concentrations, dye-dye interactions lead to a decrease in the transition dipole moments of the nondendronized species, but not of the dendronized ones. Consequently, in the high concentration range, dendronized and nondendronized species exhibit similar values of the real part of the microscopic third-order polarizability at 1550 nm. Solid-state film absorption spectra suggest that the dendrons significantly disrupt the chromophore- chromophore interactions seen for the nondendronized species, reducing, but not eliminating, linear absorption losses in the near-IR, and suppressing absorption peaks that are hypsochromically shifted from the solution spectra maximum: centrally placed dendrons have a larger effect than terminal dendronization, so that the corresponding thin-film spectra more closely resemble those seen in solution with increasing generations of dendronization. Z-scan measurements at 1550 nm indicate that the third-order susceptibility of dendronized heptamethine guest-host films depend approximately linearly on doping ratio of dyes and are in reasonable agreement with values extrapolated from solution-derived third-order polarizabilities; in contrast, the susceptibilities of films highly doped with an undendronized analogue fall short of values expected from solution polarizabilities.
