A TOTAL SYNTHESIS OF (-)-REISWIGIN A VIA SEQUENTIAL CLAISEN REARRANGEMENT INTRAMOLECULAR ESTER ENOLATE ALKYLATION

Authors
KIM DJ SHIN KJ KIM IY PARK SW
Citation
Dj. Kim et al., A TOTAL SYNTHESIS OF (-)-REISWIGIN A VIA SEQUENTIAL CLAISEN REARRANGEMENT INTRAMOLECULAR ESTER ENOLATE ALKYLATION, Tetrahedron letters, 35(43), 1994, pp. 7957-7960
Citations number
15
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
35
Issue
43
Year of publication
1994
Pages
7957 - 7960
Database
ISI
SICI code
0040-4039(1994)35:43<7957:ATSO(A>2.0.ZU;2-8
Abstract
(-)-Reiswigin A (1), a novel anti-viral diterpene, has been synthesize d in a highly stereoselective manner utilizing a sequential Claisen re arrangement - intramolecular ester enolate alkylation strategy.