Structure and stereochemistry of cyclodimers obtained by acid treatment oftrans-stilbenes and of N-1,2-diarylethylamides

Authors
Aguirre, JM Alesso, EN Iglesias, GYM
Citation
Jm. Aguirre et al., Structure and stereochemistry of cyclodimers obtained by acid treatment oftrans-stilbenes and of N-1,2-diarylethylamides, J CHEM S P1, (10), 1999, pp. 1353-1358
Citations number
18
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1
ISSN journal
0300922X → ACNP
Issue
10
Year of publication
1999
Pages
1353 - 1358
Database
ISI
SICI code
0300-922X(19990521):10<1353:SASOCO>2.0.ZU;2-5
Abstract
The reaction of trans-stilbenes and N-1,2-diarylethylamides with ethyl poly phosphate affords indanes and tetralins with three stereogenic centres. The structural and configurational assignment of the cyclodimers is based main ly on the NMR and MS data. A possible transition state for the reaction is discussed.