Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Abstract A combination of FeCl 3 and [bmim]FeCl 4 (or [bmim]PF 6 ) promotes the cyclization of homoallylic N‐tosylamine (I) with aldehydes using benzotrifluoride as the solvent.
Abstract The Sommelet–Hauser rearrangement of X-benzylic onium ylides (X = heteroatom) is an interesting transformation in organic synthesis. This rearrangement proceeds via dearomative [2,3]-sigmatropic rearrangement, followed by aromatization to form a carbon(sp2)–carbon(sp3) bond. Few advances were made in studies performed around 2000 on this rearrangement because of several competitive side reactions and structural limitations. However, studies performed in the last 15 years on the rearrangement have remarkably expanded the substrate scope and synthetic applications. In this review, the utility of the Sommelet–Hauser rearrangement and recent advances for the generation of onium ylides are described. 1 Introduction 2 Base-Induced Rearrangement 3 Transition-Metal-Catalyzed Rearrangement 4 Light-Mediated Rearrangement 5 Aryne-Induced Rearrangement 6 Conclusions and Outlook
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Abstract The rearrangement of (benzylammoniomethyl)esters of type (I) under the title conditions affords α‐aryl‐α‐amino acid derivatives (II) and generally only minor amounts of the [1,2] Stevens rearrangement products (III).