Advances in catalytic enantioselective fluorination, mono-, di-, and trifluoromethylation, and trifluoromethylthiolation reactions

X Yang, T Wu, RJ Phipps, FD Toste - Chemical reviews, 2015 - ACS Publications
1. INTRODUCTION Despite being largely absent from natural products and biological
processes, fluorine plays a conspicuous and increasingly important role within …

Good partnership between sulfur and fluorine: sulfur-based fluorination and fluoroalkylation reagents for organic synthesis

C Ni, M Hu, J Hu - Chemical Reviews, 2015 - ACS Publications
Fluorine, often called as “a small atom with a big ego”, 1 lies in the second row and the 17th
column in the periodic table of the chemical elements. This unique position in the periodic …

Sulfones as Chemical Chameleons: Versatile Synthetic Equivalents of Small‐Molecule Synthons

BM Trost, CA Kalnmals - Chemistry–A European Journal, 2019 - Wiley Online Library
Sulfones are flexible functional groups that can act as nucleophiles, electrophiles, or even
radicals. Changing the reaction conditions can completely alter the reactivity of a sulfonyl …

Asymmetric organocatalytic cyclization and cycloaddition reactions

A Moyano, R Rios - Chemical Reviews, 2011 - ACS Publications
The stereocontrolled construction of chiral carbo-and heterocycles is a topic of paramount
importance in modern organic synthesis, driven by the predominance of chiral mono-and …

Sulfones: new reagents in organocatalysis

ANR Alba, X Companyó, R Rios - Chemical Society Reviews, 2010 - pubs.rsc.org
The development of new asymmetric methodologies that afford different structures in an
enantioselective fashion is one of the most exciting goals for chemists nowadays. In this …

Asymmetric organocatalysis with sulfones

M Nielsen, CB Jacobsen, N Holub… - Angewandte Chemie …, 2010 - Wiley Online Library
Asymmetric organocatalysis has become a powerful tool for the synthesis of optically active
compounds. Whereas early research mainly focused on combining simple reagents as a …

Asymmetric synthesis with silicon‐based bulky amino organocatalysts

LW Xu, L Li, ZH Shi - Advanced Synthesis & Catalysis, 2010 - Wiley Online Library
Recent years have witnessed an explosive growth in the field of amino organocatalysis,
especially in asymmetric enamine and iminium catalysis. Except for the obvious interaction …

Enantioselective organocatalytic synthesis of fluorinated molecules

G Valero, X Companyó, R Rios - Chemistry–A European …, 2011 - Wiley Online Library
The enantioselective synthesis of fluorinated molecules has drawn much attention within the
chemical community due to its unique stereoelectronic properties. The main aim of this …

Nickel-catalyzed regio-and enantio-selective Markovnikov hydromonofluoroalkylation of 1, 3-dienes

L Liao, Y Zhang, ZW Wu, ZT Ye, XX Zhang, G Chen… - Chemical …, 2022 - pubs.rsc.org
A highly enantio-and regio-selective Markovnikov hydromonofluoro (methyl) alkylation of 1,
3-dienes was developed using redox-neutral nickel catalysis. It provided a facile strategy to …

Hydrogen bonding phase-transfer catalysis with ionic reactants: enantioselective synthesis of γ-fluoroamines

G Roagna, DMH Ascough, F Ibba… - Journal of the …, 2020 - ACS Publications
Ammonium salts are used as phase-transfer catalysts for fluorination with alkali metal
fluorides. We now demonstrate that these organic salts, specifically azetidinium triflates, are …