KIM, DJ SHIN, KJ KIM, IY PARK, SW 2024-01-21T21:31:27Z 2024-01-21T21:31:27Z 2022-01-11 1994-10-24 0040-4039 https://pubs.kist.re.kr/handle/201004/145480 (-)-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. English PERGAMON-ELSEVIER SCIENCE LTD RELATIVE CONFIGURATION WITTIG REACTION ASSIGNMENT ABSOLUTE A TOTAL SYNTHESIS OF (-)-REISWIGIN A VIA SEQUENTIAL CLAISEN REARRANGEMENT INTRAMOLECULAR ESTER ENOLATE ALKYLATION Article 10.1016/S0040-4039(00)78395-X 1 TETRAHEDRON LETTERS, v.35, no.43, pp.7957 - 7960 TETRAHEDRON LETTERS 35 43 7957 7960 scie scopus A1994PP33800019 2-s2.0-0028091969 Chemistry, Organic Chemistry Article RELATIVE CONFIGURATION WITTIG REACTION ASSIGNMENT ABSOLUTE