SYNTHESIS OF A RETINOID WITH ACETYLARYLTE TRAHYDRONAPHTHENE STRUCTUREAND AN UNUSUAL CLEAVAGE OF AN ORTHO-ACETYLTRIFLATE

Authors
HANEFELD W JUNG M
Citation
W. Hanefeld et M. Jung, SYNTHESIS OF A RETINOID WITH ACETYLARYLTE TRAHYDRONAPHTHENE STRUCTUREAND AN UNUSUAL CLEAVAGE OF AN ORTHO-ACETYLTRIFLATE, Die Pharmazie, 49(1), 1994, pp. 18-20
Citations number
27
Categorie Soggetti
Pharmacology & Pharmacy",Chemistry
Journal title
Die Pharmazie → ACNP
ISSN journal
00317144
Volume
49
Issue
1
Year of publication
1994
Pages
18 - 20
Database
ISI
SICI code
0031-7144(1994)49:1<18:SOARWA>2.0.ZU;2-J
Abstract
During the synthesis of acetyl-substituted retinoids we observed an un usual bond-cleavage of an ortho-acetyltriflate. The elimination of tri fluormethansulfinate resulted in the formation of an anellated 1,2-dih ydrofuran-3-one.