Introduction Cationic domino reactions Anionic domino reactions Radical domino reactions Pericyclic domino reactions Photochemically induced domino processes Transition metal catalysis Domino reactions initiated by oxidation or reduction Enzymes in domino reactions Multicomponent reactions Special techniques in domino reactions

Domino Reactions in Organic Synthesis

BINOL: A Versatile Chiral Reagent

Stereochemical Control in Organic-Synthesis Using Silicon-Containing Compounds

Recent Developments in the Application of Oxazoline-Containing Ligands in Asymmetric Catalysis

The Concise Guide to PHARMACOLOGY 2017/18 provides concise overviews of the key properties of nearly 1800 human drug targets with an emphasis on selective pharmacology (where available), plus links to an open access knowledgebase of drug targets and their ligands (www.guidetopharmacology.org), which provides more detailed views of target and ligand properties. Although the Concise Guide represents approximately 400 pages, the material presented is substantially reduced compared to information and links presented on the website. It provides a permanent, citable, point-in-time record that will survive database updates. The full contents of this section can be found at http://onlinelibrary.wiley.com/doi/10.1111/bph.13878/full. G protein-coupled receptors are one of the eight major pharmacological targets into which the Guide is divided, with the others being: ligand-gated ion channels, voltage-gated ion channels, other ion channels, nuclear hormone receptors, catalytic receptors, enzymes and transporters. These are presented with nomenclature guidance and summary information on the best available pharmacological tools, alongside key references and suggestions for further reading. The landscape format of the Concise Guide is designed to facilitate comparison of related targets from material contemporary to mid-2017, and supersedes data presented in the 2015/16 and 2013/14 Concise Guides and previous Guides to Receptors and Channels. It is produced in close conjunction with the Nomenclature Committee of the Union of Basic and Clinical Pharmacology (NC-IUPHAR), therefore, providing official IUPHAR classification and nomenclature for human drug targets, where appropriate.

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THE CONCISE GUIDE TO PHARMACOLOGY 2017/18: G protein-coupled receptors

A Diastereocontrolled Synthesis of (+)-Febrifugine: A Potent Antimalarial Piperidine Alkaloid

Back to the Sugars: A New Enantio and Diastereocontrolled Route to Hexoses from Furfural

Child's play! Allyl ethers as protecting groups for hydroxyl functions can be removed readily with a combination of DIBAL and catalytic amounts of [NiCl2 (dppp)] Propene is expelled in this remarkably selective reaction, and a nickel-catalyzed hydroalumination-elimination pathway is proposed [Eq (a)] dppp=propane-1,3-diylbis(diphenylphosphane)

Extremely Facile and Selective Nickel‐Catalyzed Allyl Ether Cleavage

Preparation of olefins and acetylenes via reductive elimination with SmI2-HMPA

7,7-Dimethyl-6,8-dioxabicyclo[3.3.0]oct-3-en-2-one as a synthetic equivalent of ketodicyclopentadiene: a new route to (−)-physostigmine, (−)-physovenine, and (−)-aphanorphine

Takahiko Taniguchi

Papers

A Diastereocontrolled Synthesis of (+)-Febrifugine: A Potent Antimalarial Piperidine Alkaloid

Back to the Sugars: A New Enantio and Diastereocontrolled Route to Hexoses from Furfural

Extremely Facile and Selective Nickel‐Catalyzed Allyl Ether Cleavage

Preparation of olefins and acetylenes via reductive elimination with SmI2-HMPA

7,7-Dimethyl-6,8-dioxabicyclo[3.3.0]oct-3-en-2-one as a synthetic equivalent of ketodicyclopentadiene: a new route to (−)-physostigmine, (−)-physovenine, and (−)-aphanorphine