Palladium catalyzed C–C and C–N bond forming reactions: an update on the synthesis of pharmaceuticals from 2015–2020
Some of the most prominent and promising catalysts in organic synthesis for the requisite
construction of C–C and C–N bonds are palladium (Pd) catalysts, which play a pivotal role in …
construction of C–C and C–N bonds are palladium (Pd) catalysts, which play a pivotal role in …
Recent applications of palladium‐catalyzed coupling reactions in the pharmaceutical, agrochemical, and fine chemical industries
C Torborg, M Beller - Advanced Synthesis & Catalysis, 2009 - Wiley Online Library
Palladium‐catalyzed coupling reactions have become a central tool for the synthesis of
biologically active compounds both in academia and industry. Most of these transformations …
biologically active compounds both in academia and industry. Most of these transformations …
Few-layer graphdiyne doped with sp-hybridized nitrogen atoms at acetylenic sites for oxygen reduction electrocatalysis
Y Zhao, J Wan, H Yao, L Zhang, K Lin, L Wang… - Nature …, 2018 - nature.com
The oxygen reduction reaction (ORR) is a fundamental reaction for energy storage and
conversion. It has mainly relied on platinum-based electrocatalysts, but the chemical doping …
conversion. It has mainly relied on platinum-based electrocatalysts, but the chemical doping …
Copper-free Sonogashira cross-coupling reactions: an overview
The Sonogashira reaction is a cross-coupling reaction of a vinyl or aryl halide with a terminal
alkyne to form a C–C bond. In its original form, the Sonogashira reaction is performed with a …
alkyne to form a C–C bond. In its original form, the Sonogashira reaction is performed with a …
Kinetic isotope effects in the study of organometallic reaction mechanisms
M Gomez-Gallego, MA Sierra - Chemical reviews, 2011 - ACS Publications
Kinetic Isotope Effects in the Study of Organometallic Reaction Mechanisms | Chemical
Reviews ACS ACS Publications C&EN CAS Find my institution Log In Chemical Reviews ACS …
Reviews ACS ACS Publications C&EN CAS Find my institution Log In Chemical Reviews ACS …
The Sonogashira reaction: a booming methodology in synthetic organic chemistry
R Chinchilla, C Nájera - Chemical reviews, 2007 - ACS Publications
The array of transition-metal-catalyzed cross-coupling reactions can easily be considered
nowadays cornerstones in the field of organic synthesis. 1, 2 Among them, the palladium …
nowadays cornerstones in the field of organic synthesis. 1, 2 Among them, the palladium …
Domino reactions in organic synthesis
LF Tietze - Chemical reviews, 1996 - ACS Publications
Synthetic organic chemistry has developed in a fascinating way over the past decades.
Several highly selective procedures have been developed which allow the preparation of …
Several highly selective procedures have been developed which allow the preparation of …
C H Activation: A Complementary Tool in the Total Synthesis of Complex Natural Products
The recent advent of transition‐metal mediated C H activation is revolutionizing the
synthetic field and gradually infusing a “C H activation mind‐set” in both students and …
synthetic field and gradually infusing a “C H activation mind‐set” in both students and …
Palladium and copper catalyzed Sonogashira cross coupling an excellent methodology for CC bond formation over 17 years: A review
Sonogashira coupling involves coupling of vinyl/aryl halides with terminal acetylenes
catalyzed by transition metals, especially palladium and copper. This is a well known …
catalyzed by transition metals, especially palladium and copper. This is a well known …
Palladium‐based catalytic systems for the synthesis of conjugated enynes by Sonogashira reactions and related alkynylations
H Doucet, JC Hierso - Angewandte Chemie International …, 2007 - Wiley Online Library
Conjugated alkynes are recurring building blocks in natural products, a wide range of
industrial intermediates, pharmaceuticals and agrochemicals, and molecular materials for …
industrial intermediates, pharmaceuticals and agrochemicals, and molecular materials for …