Results 101 to 110 of about 12,531 (256)
The coordination of α‐methyl‐β‐amidoitaconate at Rh(I) diphosphine complexes is studied using a combination of high‐field and low‐field flow NMR spectroscopy and X‐ray analysis. In the presence of basic or acidic additives, the formation of neutral Rh(I) or Rh(III) complexes occurs.
Neeraja M. Kaimal +3 more
wiley +1 more source
Quantifying Anisole Dimer Interactions in Solution With a Molecular Balance
Dispersion‐driven anisole stacking overcomes steric repulsion to favor folded cyclooctatetraene valence‐bond isomers in solution. We report a combined experimental and computational study that quantifies the interaction strength of anisole–anisole stacking in solution using a 1,4/1,6‐dianisole‐substituted cyclooctatetraene (COT) molecular balance.
Marvin H. J. Domanski +3 more
wiley +1 more source
Isotelluroureas for Asymmetric C1 Ammonium Enolate Reactions
Chiral isotelluroureas are powerful catalysts for a variety of C─C bond forming C1 ammonium enolate transformations. Isotelluroureas (ITeUs) have recently been introduced as a novel class of highly nucleophilic Lewis base catalysts. Herein, we systematically screened them for their potential to facilitate C1 ammonium enolate transformations and ...
Fereshteh Khorasani +3 more
wiley +1 more source
Diastereoselective Synthesis of Highly Substituted Methylene Cyclobutanes by Pd Catalysis
A chemo‐ and diastereoselective palladium‐catalyzed intramolecular coupling/cyclization of borylated 1,5‐dienes, readily accessible by allene allylboration, with iodoarenes enables the synthesis of highly substituted methylene cyclobutanes. The method exhibits broad scope, high functional group tolerance, and complete enantiospecificity.
Jose M. Malga +1 more
wiley +1 more source
Retro‐Hetero‐Michael Addition Strategies in Organic Synthesis
In this review, synthetic approaches to carbo‐ and heterocyclic compounds, including natural products, published in the last 15 years (2011–2025) which have either relied upon or included a retro‐hetero‐Michael addition step at any stage are discussed.
Dina Scarpi, Ernesto G. Occhiato
wiley +1 more source
Mechanistic Dichotomy in Enantioselective Pd‐Catalyzed Alkylation of Pyrroles With Diazoesters
Ligand‐controlled mechanistic divergence controls the Pd‐catalyzed asymmetric alkylation of pyrroles with diazoesters. While bipyridine ligands promote a conventional metal‐carbene pathway, bipyridine‐N,N′‐dioxide ligands redirect catalysis through electrophilic CH metalation before carbene transfer.
Vladimir Yu. Vaganov +5 more
wiley +1 more source
A new dual‐ligand rhodium catalytic system based on [RhCl(cod)]2, BINAP or BIPHEP, and a diphosphoramidite ligand enables the hydroformylation of olefins using paraformaldehyde as a syngas surrogate. The system efficiently converts vinyl arenes, alkyl olefins, cyclopentene, and allyl acetate with high activity and regioselectivity.
Carmela G. Arena
wiley +1 more source
An efficient and straightforward methodology for the stereoselective and diastereospecific aminosilylation and hydrosilylation of heterobicyclic norbornene derivatives is introduced. The mild conditions enable the functionalization of norbornene substrates with broad functional‐group tolerance.
Daniel Kamzol +3 more
wiley +1 more source
Enantioselective titanium-catalyzed cycloadditions of thiophene-<i>S</i>,<i>S</i>-dioxides with indenes. [PDF]
Tian P +5 more
europepmc +1 more source

