162210-58-4Relevant academic research and scientific papers
A TOTAL SYNTHESIS OF (-)-REISWIGIN A VIA SEQUENTIAL CLAISEN REARRANGEMENT-INTRAMOLECULAR ESTER ENOLATE ALKYLATION
Kim, Deukjoon,Shin, Kye Jung,Kim, Ik Yoen,Park, Sang Woo
, p. 7957 - 7960 (1994)
(-)-Reiswigin A (1), a novel anti-viral diterpene, has been synthesized in a highly stereoselective manner utilizing a sequential Claisen rearrangement intramolecular ester enolate alkylation strategy.
