Results 281 to 290 of about 157,130 (323)

Correction: Critical assessment of copper-alginate hydrogel beads as recyclable and heterogeneous catalysts for aqueous azide‒alkyne cycloaddition. [PDF]

Front Chem
Moglie Y, Buxaderas E, González Cabrera A, Díaz DD.   +3 more
europepmc   +1 more source

PhotoinducedAsymmetric [4 + 2] Cycloaddition of Benzocyclobutenoneswith Ketones into 3,4-Dihydroisocoumarins

Hansen Zhao (3236043), Xi Lu (288663), Liangkun Yang (8366904), Sile Li (21786627), Xiaoming Feng (332783), Weidi Cao (2164093)   +5 more
openalex   +1 more source

Propellane-free access to bicyclo[1.1.1]pentanes. [PDF]

Nat Commun
Liu C, Li W, Li R, Merchant RR, Kanda Y, Qin T.   +5 more
europepmc   +1 more source

Divergent Transformations of Cobaltacyclobutenes Generated from [2 + 2]-Cycloadditions of Vinylidenes and Alkynes. [PDF]

ACS Catal
Biswas S, Xiu W, Soliven A, Uyeda C.
europepmc   +1 more source

Biomimetic total synthesis of ten <i>Securinega</i> alkaloids.

Org Chem Front
Waddell LJN, Jiang Z, Grogan G, Lichman BR, Unsworth WP.   +4 more
europepmc   +1 more source

Borane-functionalized heteroscorpionate copper complexes as catalysts for azide-alkyne cycloaddition.

Dalton Trans
Cruz TFC, López-Sánchez B, Lemos MANDA, Romerosa A, Martins LMDRS.   +4 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
openaire   +2 more sources

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