| Literature DB >> 29978923 |
Martin J Wanner1, Luuk Steemers1, Michiel T Uiterweerd1, Raquel S Klijn1, Andreas W Ehlers1,2, Jan H van Maarseveen1.
Abstract
The regular bicyclic spiro motif is highly abundant given its synthetic accessibility while the diastereomer-virtually obtained through inversion at the central atom-is almost unknown. We have developed methodology to access the elusive inverted spiro architecture by employing a covalent template-directed approach. Comparison with the regular spiro bicycle analog unequivocally established the diastereomeric relationship, providing insight into the fascinating stereochemical and structural properties.Keywords: catenanes; macrocyclization; spiro compounds; stereochemistry; templated synthesis
Year: 2018 PMID: 29978923 DOI: 10.1002/chem.201803356
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236