STEREOSPECIFIC TANDEM MICHAEL ADDITION-ALDOL CONDENSATION-LACTONIZATION REACTIONS - A ROUTE TO SPIROCYCLOPENTENOLACTONE

Authors
KITTIVARAPONG S RAJVIROONKIT S SIWAPINYOYOS T THEBTARANONTH C THEBTARANONTH Y
Citation
S. Kittivarapong et al., STEREOSPECIFIC TANDEM MICHAEL ADDITION-ALDOL CONDENSATION-LACTONIZATION REACTIONS - A ROUTE TO SPIROCYCLOPENTENOLACTONE, Synthesis, (2), 1995, pp. 136-138
Citations number
9
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Synthesis → ACNP
ISSN journal
00397881
Issue
2
Year of publication
1995
Pages
136 - 138
Database
ISI
SICI code
0039-7881(1995):2<136:STMAC>2.0.ZU;2-Z
Abstract
Spirocyclopentenolactone 7 was prepared in one pot from alpha-methylen ecyclopentenone (1) via a tandem Michael addition-aldol condensation-l actonization reactions.