Synthesis of both enantiomers of methylenolactocin, nephrosterinic acid and protolichesterinic acid via tandem aldol-lactonization reactions

Palangpon KongsaereePuttinan MeepowpanYodhathai ThebtaranonthMahidol UniversityThailand National Center for Genetic Engineering and Biotechnology2018-09-072018-09-072001-07-30Tetrahedron Asymmetry. Vol.12, No.13 (2001), 1913-1922095741662-s2.0-0035973760https://repository.li.mahidol.ac.th/handle/20.500.14594/26492Both forms of the enantiomerically pure methylenolactocin, nephrosterinic and protolichesterinic acid have been synthesized via tandem aldol-lactonization reactions from corresponding optically active itaconate-anthracene adducts. © 2001 Elsevier Science Ltd. All rights reserved.Mahidol UniversityChemical EngineeringChemistrySynthesis of both enantiomers of methylenolactocin, nephrosterinic acid and protolichesterinic acid via tandem aldol-lactonization reactionsArticleSCOPUS10.1016/S0957-4166(01)00345-7