Synthesis of grandisol, the sexual attracting insect pheromone = 곤충의 sexual pheromone인 grandisol의 합성법

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dc.contributor.authorYoung Shin Kwak-
dc.contributor.authorB S Jeong-
dc.date.accessioned2017-04-19T09:25:32Z-
dc.date.available2017-04-19T09:25:32Z-
dc.date.issued2011-
dc.identifier.issn0253-6269-
dc.identifier.uri10.1007/s12272-011-0900-yko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/10353-
dc.description.abstractIn this issue, Suh's group reported a new formal total synthesis of (±)-grandisol featuring a palladium-catalyzed 4-exo-trig cyclization. Grandisol's interesting cyclobutane structure has been a popular test model for various cyclization methods over the years. This report summarizes Suh's formal synthesis of grandisol along with a concise review of the four-membered ring cyclization strategies employed in the synthesis of grandisol.-
dc.publisherPharmaceutical Soc Korea-
dc.titleSynthesis of grandisol, the sexual attracting insect pheromone = 곤충의 sexual pheromone인 grandisol의 합성법-
dc.title.alternativeSynthesis of grandisol, the sexual attracting insect pheromone-
dc.typeArticle-
dc.citation.titleArchives of Pharmacal Research-
dc.citation.number9-
dc.citation.endPage1402-
dc.citation.startPage1399-
dc.citation.volume34-
dc.contributor.affiliatedAuthorYoung Shin Kwak-
dc.contributor.alternativeName곽영신-
dc.contributor.alternativeName정병선-
dc.identifier.bibliographicCitationArchives of Pharmacal Research, vol. 34, no. 9, pp. 1399-1402-
dc.identifier.doi10.1007/s12272-011-0900-y-
dc.description.journalClassY-
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