Review covering up to 07/2019 (−)-Parthenolide is a germacrane sesquiterpene lactone,
available in ample amounts from the traditional medical plant feverfew (Tanacetum …

The preparation of cyclic macromolecules has always represented a challenging task for
polymer science, mainly because of difficulties in connecting chain extremities together …

Winner of the PROSE Award for Chemistry & Physics 2010 Acknowledging the very best in
professional and scholarly publishing, the annual PROSE Awards recognise publishers' and …

The first enantioselective formal [5+ 4] cycloaddition is realized under palladium catalysis to
deliver benzofuran-fused nine-membered rings. These medium-sized heterocycles and …

Abstract The first catalytic formal [5+ 4] cycloaddition to prepare nine‐membered
heterocycles is presented. Under palladium catalysis, the reaction of N‐tosyl azadienes and …

Well over a decade ago, two reviews were contributed to the Organic Reactions series
covering substitution and conjugate addition reactions in organocopper chemistry. Their …

The first synthesis of the macrolide insecticide A83543A (lepicidin A) has been completed
using a Diels-Alder strategy to construct the carbocyclic framework. Diene synthesis through …

1. Introduction 5758 1.1 Naturally occurring eight-membered ring carbocycles 5758 I. 1.1
Terpenoid ring systems 5758 1.1. 2 Sesquiterpenoids 5759 1.1. 3 Diterpenoids 5759 1.1. 4 …

The state-of-the-art in stereoselective synthesis!. Thoroughly revised and updated, this
enlarged second edition offers a plethora of valuable information on methods and reagents …

Direct access to pharmaceutically attractive benzo-fused nine-membered heterocyclic
alkenes 3 with a trifluoromethyl carbinol moiety was achieved via a palladium-catalyzed …