Results 101 to 110 of about 26,473 (143)

NMR-Based Structural Analysis of Highly Substituted Pyridines From Kondrat'eva Aza-Diels-Alder Cycloadditions. [PDF]

Magn Reson Chem
Suárez-Moreno GV, Méndez F, Gutierrez-Carrillo A, Rincón-Guevara MA, Amador-Sánchez YA, Islas-Jácome A, González-Zamora E.   +6 more
europepmc   +1 more source

Expanding the application of chlorinated anilines as molecular templates to achieve a series of solid-state [2 + 2] cycloaddition reactions. [PDF]

Front Chem
White GK, Unruh DK, Groeneman RH.
europepmc   +1 more source

Exploring the versatility of heterocyclic compounds containing nitrogen atoms (triazoles): a comprehensive review. [PDF]

RSC Adv
Akram M, Tamminana R.
europepmc   +1 more source

Synthetic Methods for Four-Membered Carbocycles Bearing Emerging Fluorinated Motifs. [PDF]

Chem Asian J
Yanai H, Hoshikawa S, Kawai K, Matsumoto T.   +3 more
europepmc   +1 more source

The high potential of methyl laurate as a recyclable competitor to conventional toxic solvents in [3 + 2] cycloaddition reactions. [PDF]

Beilstein J Org Chem
Yıldırım A, Göker M.
europepmc   +1 more source

Asymmetric [3 + 2] Cycloaddition to Access 3-Pyrrolines and Their Switchable Transformations to Nine-Membered Cyclic Sulfamidates and 2H-Pyrroles. [PDF]

Adv Sci (Weinh)
Choi SM, Park JU, Kim JH.
europepmc   +1 more source

Rapid access to the core of malayamycin A by intramolecular dipolar cycloaddition. [PDF]

Beilstein J Org Chem
Liu Y, Yang Y, Yang C, Huang SH, Jin J, Hong R.   +5 more
europepmc   +1 more source

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Do Antarafacial Cycloadditions Occur? Cycloaddition of Heptafulvalene with Tetracyanoethylene

Chemistry – A European Journal, 2022
AbstractThe 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
openaire   +2 more sources

Arene–Alkene Cycloaddition

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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Advances in cycloaddition polymerizations

Chem. Soc. Rev., 2006
AbstractChemInform 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
openaire   +2 more sources