Liu, Zhiguo Yoon, Goo Cheon, Seung Hoon 2024-01-20T19:32:03Z 2024-01-20T19:32:03Z 2021-09-02 2010-04-24 0040-4020 https://pubs.kist.re.kr/handle/201004/131537 The absolute configuration of (-)-licochalcone E (1) was determined to be (S) via the first enantioselective total synthesis of the compound. The chirality in (S)-(-)-licochalcone E (1) was installed by asymmetric methylation of the Evans oxazolidinone derivatives. (C) 2010 Elsevier Ltd. All rights reserved. English PERGAMON-ELSEVIER SCIENCE LTD CHALCONES An enantioselective total synthesis of (S)-(-)-licochalcone E: determination of the absolute configuration Article 10.1016/j.tet.2010.02.089 1 TETRAHEDRON, v.66, no.17, pp.3165 - 3172 TETRAHEDRON 66 17 3165 3172 scie scopus 000276804800006 2-s2.0-77949918093 Chemistry, Organic Chemistry Article CHALCONES Enantioselective synthesis Licochalcone E Asymmetric methylation Chiral oxazolidinone