Synthesis and reactivity of propargylamines in organic chemistry

K Lauder, A Toscani, N Scalacci… - Chemical reviews, 2017 - ACS Publications
Propargylamines are a versatile class of compounds which find broad application in many
fields of chemistry. This review aims to describe the different strategies developed so far for …

Synthesis of heterocycles via palladium-catalyzed carbonylations

XF Wu, H Neumann, M Beller - Chemical Reviews, 2013 - ACS Publications
Palladium-catalyzed coupling reactions have become a powerful tool in organic synthesis. 1
Today, there are numerous applications of palladium catalysts in the preparation of …

Current applications of Suzuki–Miyaura coupling reaction in the total synthesis of natural products: an update

A Taheri Kal Koshvandi, MM Heravi… - Applied …, 2018 - Wiley Online Library
Suzuki‐Miyaura Coupling Reaction (SMCR) has been extensively used in the total synthesis
of natural products. We underscored these achievements in a report published in …

Visible‐Light‐Induced Oxidation/[3+2] Cycloaddition/Oxidative Aromatization Sequence: A Photocatalytic Strategy To Construct Pyrrolo[2,1‐a]isoquinolines

YQ Zou, LQ Lu, L Fu, NJ Chang, J Rong… - Angewandte Chemie …, 2011 - Wiley Online Library
The development of new and highly efficient strategies for the rapid construction of intricate
molecular architectures is of great importance and remains a preeminent goal in current …

Ligand‐and Solvent‐Controlled Regio‐and Chemodivergent Carbonylative Reactions

JB Peng, XF Wu - Angewandte Chemie International Edition, 2018 - Wiley Online Library
The development of highly selective procedures is one of the core goals in organic
chemistry. Among the known organic transformations, carbonylation reactions present an …

[PDF][PDF] Oxidative carbonylation as a powerful tool for the direct synthesis of carbonylated heterocycles

B Gabriele, R Mancuso, G Salerno - European Journal of Organic …, 2012 - academia.edu
Carbonylation, the incorporation of carbon monoxide into an organic substrate, is now
widely recognized as a very important tool in industrial and organic chemistry.[1, 2] It allows …

Sequential Photo-oxidative [3 + 2] Cycloaddition/Oxidative Aromatization Reactions for the Synthesis of Pyrrolo[2,1-a]isoquinolines Using Molecular Oxygen as the …

A Fujiya, M Tanaka, E Yamaguchi… - The Journal of Organic …, 2016 - ACS Publications
We report an efficient method for the synthesis of pyrrolo [2, 1-a] isoquinoline derivatives
using sequential [3+ 2] cycloaddition/oxidative aromatization reactions catalyzed by …

Asymmetric allylation by chiral organocatalyst‐promoted formal hetero‐Ene reactions of alkylgold intermediates

G Dong, M Bao, X Xie, S Jia, W Hu… - Angewandte Chemie …, 2021 - Wiley Online Library
An unprecedented catalytic asymmetric allylation of isatins and isatin‐derived ketimines is
reported enabled by a gold and chiral organocatalyst cooperative catalysis strategy. This …

Construction of 5-methyleneoxazolidine-2, 4-diones bearing modifiable halogen groups through a halopalladation strategy

H Zhan, B Chen, B Zhu, X Li, Z Han, J Sun… - Chemical …, 2023 - pubs.rsc.org
Based on a halopalladation strategy, we successfully developed a haloesterification
reaction of propargylic amides to synthesize a diverse range of 5-(halomethylene) …

Cyclisation versus 1,1‐Carboboration: Reactions of B(C6F5)3 with Propargyl Amides

RL Melen, MM Hansmann, AJ Lough… - … A European Journal, 2013 - Wiley Online Library
A series of propargyl amides were prepared and their reactions with the Lewis acidic
compound B (C6F5) 3 were investigated. These reactions were shown to afford novel …