Uncovering the neglected similarities of arynes and donor–acceptor cyclopropanes

DB Werz, AT Biju - Angewandte Chemie International Edition, 2020 - Wiley Online Library
Arynes and donor–acceptor (D–A) cyclopropanes are two classes of strained systems
having the potential for numerous applications in organic synthesis. The last two decades …

A new golden age for donor–acceptor cyclopropanes

TF Schneider, J Kaschel… - Angewandte Chemie …, 2014 - Wiley Online Library
The effective use of ring strain has been applied to considerable advantage for the
construction of complex systems. The focus here is directed towards cyclopropanes as …

Intermolecular atom transfer radical addition to olefins mediated by oxidative quenching of photoredox catalysts

JD Nguyen, JW Tucker, MD Konieczynska… - Journal of the …, 2011 - ACS Publications
Atom transfer radical addition of haloalkanes and α-halocarbonyls to olefins is efficiently
performed with the photocatalyst Ir [(dF (CF3) ppy) 2 (dtbbpy)] PF6. This protocol is …

Cycloaddition reactions of enoldiazo compounds

QQ Cheng, Y Deng, M Lankelma… - Chemical Society Reviews, 2017 - pubs.rsc.org
Enoldiazo esters and amides have proven to be versatile reagents for cycloaddition
reactions that allow highly efficient construction of various carbocycles and heterocycles …

Donor–Acceptor Cyclopropanes as an Expedient Building Block Towards the Construction of Nitrogen‐Containing Molecules: An Update

P Singh, RK Varshnaya, R Dey… - Advanced Synthesis & …, 2020 - Wiley Online Library
Nitrogen‐containing molecules are the key structural constituent of many pharmaceutical
compounds that play a pivotal role in drug development. Owing to their multifaceted …

The [3+ 3]-cycloaddition alternative for heterocycle syntheses: catalytically generated metalloenolcarbenes as dipolar adducts

X Xu, MP Doyle - Accounts of Chemical Research, 2014 - ACS Publications
Conspectus The combination of two or more unsaturated structural units to form cyclic
organic compounds is commonly referred to as cycloaddition, and the combination of two …

1, 3-Dipolar cycloadditions of azomethine imines

C Nájera, JM Sansano, M Yus - Organic & Biomolecular Chemistry, 2015 - pubs.rsc.org
Azomethine imines are considered 1, 3-dipoles of the aza-allyl type which are transient
intermediates and should be generated in situ but can also be stable and isolable …

Direct functionalization processes: A journey from palladium to copper to iron to nickel to metal-free coupling reactions

JJ Mousseau, AB Charette - Accounts of Chemical Research, 2013 - ACS Publications
The possibility of finding novel disconnections for the efficient synthesis of organic
molecules has driven the interest in developing technologies to directly functionalize C–H …

Ring opening of donor–acceptor cyclopropanes with N-nucleophiles

EM Budynina, KL Ivanov, ID Sorokin, MY Melnikov - Synthesis, 2017 - thieme-connect.com
Ring opening of donor–acceptor cyclopropanes with various N-nucleophiles provides a
simple approach to 1, 3-functionalized compounds that are useful building blocks in organic …

Phosphine-catalyzed annulations of azomethine imines: allene-dependent [3+ 2],[3+ 3],[4+ 3], and [3+ 2+ 3] pathways

R Na, C Jing, Q Xu, H Jiang, X Wu, J Shi… - Journal of the …, 2011 - ACS Publications
In this paper we describe the phosphine-catalyzed [3+ 2],[3+ 3],[4+ 3], and [3+ 2+ 3]
annulations of azomethine imines and allenoates. These processes mark the first use of …