Skip to main content

Open Access Dimere aus o-Nitrobenzylidenacetessigestern

Download Article:
Die o-Nitrobenzylidenacetessigester 1 dimerisieren in Gegenwart von BuLi oder LDA mit geringer Ausbeute zu den Cyclohexenen 2. Von 2b werden zwei Diastereomere isoliert, deren Konfiguration nmr-spektroskopisch abgeleitet wird.

Dimers from o-nitrobenzylidene acetoacetic esters

The o-nitrobenzylidene acetoacetic esters 1 dimerize in the presence of BuLi or LDA to give the cyclohexenes 2 in poor yield. Two diastereomer of 2b were isolated, whose configuration is deduced by nmr-spectroscopic methods.

Document Type: Research Article

Affiliations: 1: Institut für Pharmazeutische Chemie der Technischen Universität Braunschweig, Beethovenstraße 55, Braunschweig, D-38106, Germany, Email: [email protected] 2: Institut für Pharmazeutische Chemie der Technischen Universität Braunschweig, Braunschweig, Germany

Publication date: 01 August 2005

More about this publication?
  • Pharmazie is a leading journal in the field of pharmaceutical sciences. As a peer-reviewed scientific journal, Pharmazie is regularly indexed in the relevant databases like Web of science, Journal Citation Reports and many others. The journal is open for submissions from the whole spectrum of pharnaceutical sciences including Pharmaceutical Chemistry, Experimental and Clinical Pharmacology, Drug Analysis, Pharmaceutics, Pharmaceutical Biology, Clinical Pharmacy etc.
  • Information for Authors
  • Submit a Paper
  • Subscribe to this Title
  • Ingenta Connect is not responsible for the content or availability of external websites
  • Access Key
  • Free content
  • Partial Free content
  • New content
  • Open access content
  • Partial Open access content
  • Subscribed content
  • Partial Subscribed content
  • Free trial content