STEREOSELECTIVITY OF INTRAMOLECULAR CYCLIZATIONS OF NITRONES DERIVED FROM 3-OXAHEPT-6-ENALS

Authors
GRAVESTOCK MB KNIGHT DW LOVELL JS THORNTON SR
Citation
Mb. Gravestock et al., STEREOSELECTIVITY OF INTRAMOLECULAR CYCLIZATIONS OF NITRONES DERIVED FROM 3-OXAHEPT-6-ENALS, Journal of the Chemical Society. Perkin transactions. I, (13), 1994, pp. 1661-1663
Citations number
22
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Journal of the Chemical Society. Perkin transactions. I → ACNP
ISSN journal
0300922X
Issue
13
Year of publication
1994
Pages
1661 - 1663
Database
ISI
SICI code
0300-922X(1994):13<1661:SOICON>2.0.ZU;2-M
Abstract
Intramolecular cycloadditions of the nitrones 9 and 14 show moderate t o good stereoselections in favour of the cis-fused diastereoisomers 10 or 16, respectively.