M Murakami, N Ishida - Chemical Reviews, 2020 - ACS Publications
This article reviews synthetic transformations involving cleavage of a carbon–carbon bond of a four-membered ring, with a particular focus on the examples reported during the period …
YF Han, Y Huang, H Liu, ZH Gao, CL Zhang… - Nature …, 2022 - nature.com
Three-component carboacylation of simple alkenes with readily available reagents is challenging. Transition metal-catalysed intermolecular carboacylation works for alkenes with …
Y Xue, G Dong - Accounts of Chemical Research, 2022 - ACS Publications
Conspectus Bridged and fused rings are commonly found in biologically important molecules. Current tactics to construct these ring systems are primarily based on stepwise …
G Fumagalli, S Stanton, JF Bower - Chemical Reviews, 2017 - ACS Publications
In this review, synthetic and mechanistic aspects of key methodologies that exploit C–C single-bond cleavage of strained ring systems are highlighted. The focus is on transition …
Transition metal (TM)‐catalyzed difunctionalization of unactivated olefins with two carbon‐ based entities is a powerful method to construct complex molecular architectures rapidly …
L Souillart, N Cramer - Chemical reviews, 2015 - ACS Publications
The cleavage and reorganization of carbon− carbon bonds is an industrial key technology for crude oil refining, carried out on a massive scale. In contrast, C− C bond cleavage …
The transition-metal-catalyzed “cut and sew” transformation has recently emerged as a useful strategy for preparing complex molecular structures. After oxidative addition of a …
M Murakami, N Ishida - Journal of the American Chemical Society, 2016 - ACS Publications
Conventional organic synthesis has been mainly based upon the reactivities of π-bonds and polar σ-bonds. Carbon–carbon single bonds are nonpolar and generally far less reactive …
A remaining challenge in the synthetic chemistry field is formation of all-carbon quaternary centers, a feature found in many natural products, particularly in spirocycle systems. 1 …