BROMINATION-DEHYDROBROMINATION ROUTE TO SOME NATURALLY-OCCURRING 1,6-DIOXASPIRO[4,4]-NONENES AND 1,6-DIOXASPIRO[4,4]-NONADIENES

Authors
TU YQ BYRIEL KA KENNARD CHL KITCHING W
Citation
Yq. Tu et al., BROMINATION-DEHYDROBROMINATION ROUTE TO SOME NATURALLY-OCCURRING 1,6-DIOXASPIRO[4,4]-NONENES AND 1,6-DIOXASPIRO[4,4]-NONADIENES, Journal of the Chemical Society. Perkin transactions. I, (10), 1995, pp. 1309-1315
Citations number
21
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Journal of the Chemical Society. Perkin transactions. I → ACNP
ISSN journal
0300922X
Issue
10
Year of publication
1995
Pages
1309 - 1315
Database
ISI
SICI code
0300-922X(1995):10<1309:BRTSN1>2.0.ZU;2-K
Abstract
Bromination-dehydrobromination of saturated 1,6-dioxaspiro[4.4]nonanes afforded a variety of naturally occurring 1,6-dioxaspiro[4.4]-nonenes and -nonadienes, such as 2-5 and 8, and can be applied to give unsatu rated spirolactones, such as 27.