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 …
fields of chemistry. This review aims to describe the different strategies developed so far for …
Titanium catalysis for the synthesis of fine chemicals–development and trends
Titanium is the second most abundant transition metal and is already a key player in
important industrial processes (eg polyethylene). Titanium is an attractive metal to use for …
important industrial processes (eg polyethylene). Titanium is an attractive metal to use for …
Modern applications of low-valent early transition metals in synthesis and catalysis
Low-valent early transition metals are often intrinsically highly reactive as a result of their
strong propensity toward oxidation to more stable high-valent states. Harnessing these …
strong propensity toward oxidation to more stable high-valent states. Harnessing these …
Synthesis of chiral cyclopentenones
SP Simeonov, JPM Nunes, K Guerra… - Chemical …, 2016 - ACS Publications
The cyclopentenone unit is a very powerful synthon for the synthesis of a variety of bioactive
target molecules. This is due to the broad diversity of chemical modifications available for …
target molecules. This is due to the broad diversity of chemical modifications available for …
[PDF][PDF] Recent advances in the Pauson–Khand reaction and related [2+ 2+ 1] cycloadditions
KM Brummond, JL Kent - Tetrahedron, 2000 - uwindsor.ca
The Pauson±Khand (P±K) reaction, formally a [21211] cycloaddition involving an alkene, an
alkyne and carbon monoxide moieties to form a cyclopentenone, was first discovered in the …
alkyne and carbon monoxide moieties to form a cyclopentenone, was first discovered in the …
The Pauson–Khand reaction: the catalytic age is here!
SE Gibson, A Stevenazzi - Angewandte Chemie International …, 2003 - Wiley Online Library
As a consequence of growing environmental awareness, it is now inappropriate to design a
synthetic metal‐mediated transformation that involves a noncatalytic use of toxic and …
synthetic metal‐mediated transformation that involves a noncatalytic use of toxic and …
In the arena of enantioselective synthesis, titanium complexes wear the laurel wreath
DJ Ramon, M Yus - Chemical reviews, 2006 - ACS Publications
Asymmetry is ubiquitous in every part of Nature1 and has a great impact in many fields, not
only in chemistry but also even in arts. In the pharmaceutical area, asymmetry plays an …
only in chemistry but also even in arts. In the pharmaceutical area, asymmetry plays an …
CO-Transfer carbonylation reactions. a catalytic Pauson− Khand-Type reaction of enynes with aldehydes as a source of carbon monoxide
T Morimoto, K Fuji, K Tsutsumi… - Journal of the American …, 2002 - ACS Publications
The reaction of enynes with aldehydes in the presence of a catalytic amount of [RhCl (cod)]
2/dppp results in the Pauson− Khand-type reaction without the use of gaseous carbon …
2/dppp results in the Pauson− Khand-type reaction without the use of gaseous carbon …
Saturated nitrogen heterocycles
A Mitchinson, A Nadin - Journal of the Chemical Society, Perkin …, 2000 - pubs.rsc.org
Saturated nitrogen heterocycles - Journal of the Chemical Society, Perkin Transactions 1 (RSC
Publishing) DOI:10.1039/A908537H Royal Society of Chemistry View PDF VersionPrevious …
Publishing) DOI:10.1039/A908537H Royal Society of Chemistry View PDF VersionPrevious …
Iridium− Chiral Diphosphine Complex Catalyzed Highly Enantioselective Pauson-Khand-Type Reaction
T Shibata, K Takagi - Journal of the American Chemical Society, 2000 - ACS Publications
The transition metal-mediated carbonylative coupling reaction is one of the most important
carbon skeleton-forming reactions, and provides cyclic compounds with a carbonyl group …
carbon skeleton-forming reactions, and provides cyclic compounds with a carbonyl group …