Results 21 to 30 of about 216,387 (290)
Relative Reactivity of the Metal-Amido versus Metal-Imido Bond in Linked Cp-Amido and Half-Sandwich Complexes of Vanadium [PDF]
Treatment of (η5-C5H4C2H4NR)V(N-t-Bu)Me (R = Me, i-Pr) and CpV(N-p-Tol)(N-i-Pr2)Me (Cp = η5-C5H5) with B(C6F5)3 or [Ph3C][B(C6F5)4] results in formation of the corresponding cations, [(η5-C5H4C2H4NR)V(N-t-Bu)]+ and [CpV(N-p-Tol)(N-i-Pr2)]+.
Alonso F.+31 more
core +5 more sources
An overview of the cycloaddition chemistry of fulvenes and emerging applications
The unusual electronic properties and unique reactivity of fulvenes have interested researchers for over a century. The propensity to form dipolar structures at relatively low temperatures and to participate as various components in cycloaddition ...
Ellen Swan+2 more
doaj +1 more source
Computational and Spectral Investigation of 5,12-Dihydro-5,12-ethanonaphthacene-13-carbaldehyde
A conformational search of 5,12-dihydro-5,12-ethanonaphthacene-13-carbaldehyde predicted the presence of twelve conformations. The geometry of the twelve conformations established at the B3LYP/6-31G* level showed only six unique ones.
Abdulrahman I. Almansour+5 more
doaj +1 more source
Cycloaddition an Benzvalen [PDF]
AbstractBenzvalen (I) reagiert in ätherischer Lösung mit den Benzonitriloxiden (II) zu den Addukten (IIIa).
openaire +4 more sources
Cycloadditions to 1,1‐Dicyclopropylethylene [PDF]
While the stabilization of cationic centers by alpha cyclopropyl groups has been verified in many instances [2,31, to the best of our knowledge nothing is known about the influenceof cyclopropyl groups, as substituents, on the reaction mechanism of multiple bonds. The α-cyclopropylcarbonium ions 141 that may be formed are capable of rearrangement, thus
Effenberger, Franz, Podszun, Wolfgang
openaire +4 more sources
Alkyne–Alkene [2 + 2] cycloaddition based on visible light photocatalysis
UV-activated alkyne–alkene [2 + 2] cycloaddition has served as an important tool to access cyclobutenes. Although broadly adopted, the limitations with UV light as an energy source prompted us to explore an alternative method.
Sujin Ha+6 more
semanticscholar +1 more source
[2 + 2 + 2] cycloaddition of a 1,2-bis(propiolyl)benzene derivative with terminal and internal alkynes takes place in the presence of [Ir(cod)Cl]2 (cod = 1,5-cyclooctadiene) combined with bis(diphenylphosphino)ethane (DPPE) to give anthraquinones in 42 ...
Takahiro Sawano+2 more
doaj +1 more source
Polar Diels-Alder Reactions using Heterocycles as Electrophiles. Influence of Microwave Irradiation [PDF]
In this work we studied a series of polar Diels-Alder reactions using different heterocycles derivatives acting as electrophiles joint to dienes of different nucleophilicity, analyzing the effect of the microwave irradiation in these processes. We employ
Della Rosa, Claudia Daniela+3 more
core +1 more source
In the title compounds, C32H25ClN2O4 (I) and C33H28N2O5 (II), the six-membered pyran and piperidine rings adopt envelope and chair conformations, respectively. The five-membered pyrrolidine rings adopt twist conformations. Compound (II) crystallizes with
S. Syed Abuthahir+4 more
doaj +1 more source
Donor-Acceptor Substituted Benzo-, Naphtho- and Phenanthro-Fused Norbornadienes
The photochromic norbornadiene/quadricyclane (NBD/QC) couple has found interest as a molecular solar thermal energy (MOST) system for storage of solar energy.
Mads Mansø+4 more
doaj +1 more source