Asymmetric catalytic rearrangements with α-diazocarbonyl compounds
S Dong, X Liu, X Feng - Accounts of Chemical Research, 2022 - ACS Publications
Conspectus α-Diazocarbonyl compounds serve as nucleophiles, dipoles, carbene
precursors, and rare electrophiles, enabling a vast array of organic transformations under …
precursors, and rare electrophiles, enabling a vast array of organic transformations under …
Homogeneous gold-catalyzed oxidation reactions
Homogeneous gold catalysis has experienced extraordinary development since the dawn of
this millennium. Oxidative gold catalysis is a vibrant and fertile subfield and has over the …
this millennium. Oxidative gold catalysis is a vibrant and fertile subfield and has over the …
N-Triftosylhydrazones: A New Chapter for Diazo-Based Carbene Chemistry
Z Liu, P Sivaguru, G Zanoni, X Bi - Accounts of Chemical …, 2022 - ACS Publications
Conspectus Over recent decades, N-sulfonylhydrazones have attracted significant attention
in academic and industrial contexts owing to their ease of preparation, versatile reactivity …
in academic and industrial contexts owing to their ease of preparation, versatile reactivity …
Transition-metal-catalyzed cross-couplings through carbene migratory insertion
Y Xia, D Qiu, J Wang - Chemical reviews, 2017 - ACS Publications
Transition-metal-catalyzed cross-coupling reactions have been well-established as
indispensable tools in modern organic synthesis. One of the major research goals in cross …
indispensable tools in modern organic synthesis. One of the major research goals in cross …
Gold-catalyzed synthesis of small rings
M Mato, A Franchino, C Garcı́a-Morales… - Chemical …, 2020 - ACS Publications
Three-and four-membered rings, widespread motifs in nature and medicinal chemistry, have
fascinated chemists ever since their discovery. However, due to energetic considerations …
fascinated chemists ever since their discovery. However, due to energetic considerations …
Modern organic synthesis with α-diazocarbonyl compounds
A Ford, H Miel, A Ring, CN Slattery, AR Maguire… - Chemical …, 2015 - ACS Publications
In 1994, Ye and McKervey published a paper in Chemical Reviews entitled “Organic
Synthesis with α-Diazocarbonyl Compounds”. 1 Our intention then was to draw attention to …
Synthesis with α-Diazocarbonyl Compounds”. 1 Our intention then was to draw attention to …
C H Bond Functionalization: Emerging Synthetic Tools for Natural Products and Pharmaceuticals
J Yamaguchi, AD Yamaguchi… - Angewandte Chemie …, 2012 - Wiley Online Library
The direct functionalization of C H bonds in organic compounds has recently emerged as a
powerful and ideal method for the formation of carbon–carbon and carbon–heteroatom …
powerful and ideal method for the formation of carbon–carbon and carbon–heteroatom …
C–C bond cleavages of cyclopropenes: operating for selective ring-opening reactions
R Vicente - Chemical Reviews, 2020 - ACS Publications
This review highlights key reactivities relying on C–C bond cleavages of cyclopropenes.
Metal-catalyzed and metal-free transformations are covered in reactions involving direct ring …
Metal-catalyzed and metal-free transformations are covered in reactions involving direct ring …
Catalytic enantioselective aldol reactions
Y Yamashita, T Yasukawa, WJ Yoo… - Chemical Society …, 2018 - pubs.rsc.org
Recent developments in catalytic asymmetric aldol reactions have been summarized.
Enantioselective aldol reactions are important methods to synthesize β-hydroxy carbonyl …
Enantioselective aldol reactions are important methods to synthesize β-hydroxy carbonyl …
Metal-catalyzed CH activation/functionalization: The fundamentals
F Roudesly, J Oble, G Poli - Journal of Molecular Catalysis A: Chemical, 2017 - Elsevier
An isolated Csingle bondH bond in a molecule has a very low reactivity owing to the large
kinetic barrier associated to the Csingle bondH bond cleavage and the apolar nature of this …
kinetic barrier associated to the Csingle bondH bond cleavage and the apolar nature of this …