Journal ArticleDOI
CLXXI.—Dehydro-2-naphtholsulphone
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This article is published in Journal of The Chemical Society (resumed).The article was published on 1930-01-01. It has received 41 citations till now.read more
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Mechanistic Manifold and New Developments of the Julia–Kocienski Reaction
TL;DR: The Julia-Kocienski reaction has become indispensable in the synthetic organic chemist's olefination toolbox as discussed by the authors, although the stereochemical outcome of the transformation is sometimes difficult to predict.
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Evolution of asymmetric organocatalysis: multi- and retrocatalysis
TL;DR: The impressive advantages of asymmetric organomulticatalysis are highlighted, the development of its development is examined, and detailed reactions based on the catalyst classes employed are presented, ranging from the very beginnings to the latest multicatalyst systems.
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Asymmetric organocatalysis with sulfones.
TL;DR: Sulfones have become especially important substrates in the field of organocatalysis because of the many transformation possibilities and their ability to generate both nucleophilic and electrophilic reaction partners.
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Radical-Mediated Remote Functional Group Migration.
Xinxin Wu,Chen Zhu +1 more
TL;DR: The FGM strategy proves to be an ingenious tool for radical-mediated functionalization of remote unactivated C(sp3)-H bonds and direct elaboration of C-H bonds into the targeted functional groups represents one of the most ideal and straightforward methods for molecular functionalization.
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Modern Aspects of the Smiles Rearrangement.
TL;DR: The Smiles rearrangement is an intramolecular SNAr reaction, breaking a C−X single bond and forming a new C−C bond though ipso substitution as mentioned in this paper.