Results 181 to 190 of about 83,738 (273)
Enantioselective synthesis of C-C and C-N axially chiral pyrazole-based heterobiaryls. [PDF]
He J, Yang Z, Lin L, Feng X.
europepmc +1 more source
Highly Diastereo- and Enantioselective Allylboration of Aldehydes using alpha-Substituted Allyl/Crotyl Pinacol Boronic Esters via in Situ Generated Borinic Esters [PDF]
Althaus M. +60 more
core +1 more source
Gold(I)‐Catalyzed Domino Cyclization for the Construction of Trispirocyclic Cyclohexanes
We describe herein a series of intricate trispirocyclic architectures that have been synthesized from readily available substrates through an operationally simple one‐pot transformation under mild conditions. An unprecedented gold(I)‐catalyzed domino cyclization involving 2‐ethynylbenzyl alcohol derivatives and heterocyclic α,β‐unsaturated imines ...
Manon Genet +3 more
wiley +1 more source
Unified Enantioselective Synthesis of 5-Phenylmorphans and <i>cis</i>-Octahydroisoquinolines. [PDF]
Mahgoub AA +3 more
europepmc +1 more source
Why add another catalyst when the product itself holds the power to catalyze its own formation? Autocatalysis in synthetic chemistry enhances reaction efficiency and uncovers novel catalytic behavior across both closed‐shell and open‐shell systems, expanding reactivity and enabling innovative design strategies.
Jaspreet Kaur, Joshua P. Barham
wiley +1 more source
Copper-catalyzed enantioselective synthesis of γ-butenolides via radical diversification of allenoic acid. [PDF]
Han B, Nie Z, Ye C, Bao H.
europepmc +1 more source
Pd(II)‐Catalyzed Strategies for the β‐Arylation of α‐Amino Acids: An Overview
The graphical abstract summarizes the review “Pd(II)‐Catalyzed Strategies for the β‐Arylation of α‐Amino Acids: An Overview”, highlighting representative Pd(II)‐catalyzed methods for the β‐arylation of α‐amino acids. Key mechanistic features, substrate diversity, and synthetic relevance of these transformations are showcased. Abstract Metal‐catalyzed C─
Davide Illuminati +4 more
wiley +1 more source
Highly enantioselective synthesis controlled by spin-exchange interaction. [PDF]
Yan Y +4 more
europepmc +1 more source
Highly stereoenriched α‐trifluoromethoxylated sulfoxides were accessed from racemic aryl methyl sulfoxides, by means of a trifluoromethoxylative Pummerer rearrangement and a highly enantioselective sulfoxidation. The 2‐step procedure could be performed in one pot.
Nicolas Moget +6 more
wiley +1 more source

