Results 181 to 190 of about 27,486 (241)
C3-H methylenephosphonylation of azaarenes enabled by catalyst-controlled regioselective cyclizative rearrangement. [PDF]
Chem SciLiu D, Li FZ, He YP, Wu H.
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Visible-light-enabled excited-state dearomatization reactions. [PDF]
Sci AdvLi M, Cheng YZ, You SL.
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Advances in cycloaddition polymerizations
Chem. Soc. Rev., 2006AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Glenn W, Goodall, Wayne, Hayes
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Do Antarafacial Cycloadditions Occur? Cycloaddition of Heptafulvalene with Tetracyanoethylene
Chemistry – A European Journal, 2022AbstractThe cycloaddition of heptafulvalene (1) with tetracyanoethylene (TCNE) was previously described as an example of an antarafacial cycloaddition, a [π14a+π2s] process that afforded only the trans cycloadduct by virtue of the edge‐to‐face approach of TCNE, facilitated by the S shape of 1.
Anthony R. Izzotti, James L. Gleason
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Dynamics of Carbene Cycloadditions
Journal of the American Chemical Society, 2011Quasiclassical trajectory calculations using quantum mechanical energies and forces generated by the Venus and Gaussian programs provide for the first time a detailed dynamical picture of singlet carbene, CCl(2) and CF(2), cycloadditions to alkenes on the B3LYP/6-31G* surface.
Lai, Xu, Charles E, Doubleday, K N, Houk
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Cycloaddition of Fluorinated Oxazoles.
ChemInform, 2005AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
N. V. Vasil'ev +5 more
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Chemical Reviews, 2016
Cycloadditions are among the most efficient chemical processes, combining atom economy, stereospecificity, and the ability to generate molecular complexity in a single step. Aromatic rings would in principle be ideal reaction partners, as they contain, at least from the topological point of view, both olefinic and diene subunits; however, the stability
Remy Richard, Bochet Christian G
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Cycloadditions are among the most efficient chemical processes, combining atom economy, stereospecificity, and the ability to generate molecular complexity in a single step. Aromatic rings would in principle be ideal reaction partners, as they contain, at least from the topological point of view, both olefinic and diene subunits; however, the stability
Remy Richard, Bochet Christian G
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Cycloadditions with Metauo-Phosphaalkenes
Phosphorus, Sulfur, and Silicon and the Related Elements, 1994Abstract Cycloadditions of metallo-phosphaalkenes such as (C5Me5)(C0)2Fe− P=CR1R2 (R1 = R2 = SiMe3, NMe2; R1 = Ph, R2 = SiMe3) are performed with isocyanides, electron-poor alkenes, alkynes and heteroal ...
Weber, Lothar +2 more
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