%0 Journal Article %T Stereodivergent approach in the protected glycal synthesis of L-vancosamine, L-saccharosamine, L-daunosamine and L-ristosamine involving a ring-closing metathesis step %+ Institut des Sciences Chimiques de Rennes (ISCR) %+ Institut des Molécules et Matériaux du Mans (IMMM) %+ Chimie Et Interdisciplinarité : Synthèse, Analyse, Modélisation (CEISAM) %A Nocquet, Pierre-Antoine %A Macé, Aurélie %A Legros, Frédéric %A Lebreton, Jacques %A Dujardin, Gilles %A Collet, Sylvain %A Martel, Arnaud %A Carboni, Bertrand %A Carreaux, François %Z University of Rennes 1 %Z Centre National de la Recherche Scientifique (CNRS) %Z ANR [ANR-14-CE06-0008-01] %< avec comité de lecture %@ 1860-5397 %J Beilstein Journal of Organic Chemistry %I Beilstein-Institut %V 14 %P 2949-2955 %8 2018 %D 2018 %R 10.3762/bjoc.14.274 %M 30546479 %K diastereoselective additions to aldehydes %K pluramycins %K ring-closing metathesis %K 3-amino glycals %K vinyl ethers %Z Chemical Sciences/Organic chemistryJournal articles %X In this paper, a new access to several chiral 3-aminoglycals as potential precursors for glycosylated natural products is reported from a common starting material, (-)-methyl-L-lactate. The stereodivergent strategy is based on the implementation of a ring-closing metathesis of vinyl ethers as key step of reaction sequences developed. %G English %2 https://univ-rennes.hal.science/hal-01973903/document %2 https://univ-rennes.hal.science/hal-01973903/file/1860-5397-14-274.pdf %L hal-01973903 %U https://univ-rennes.hal.science/hal-01973903 %~ UNIV-NANTES %~ UNIV-RENNES1 %~ CNRS %~ UNIV-LEMANS %~ INSA-RENNES %~ ENSC-RENNES %~ ISCR %~ SCR_ICMV %~ STATS-UR1 %~ UR1-SPM %~ INC-CNRS %~ UR1-UFR-SPM %~ UR1-HAL %~ ISCR-CORINT %~ UR1-SDLM %~ TEST-UR-CSS %~ UNIV-RENNES %~ INSA-GROUPE %~ ISCR-CORINT1 %~ IMMM-LEMANS %~ TEST-HALCNRS %~ ANR %~ UR1-MMS %~ CEISAM %~ NANTES-UNIVERSITE %~ UNIV-NANTES-AV2022 %~ TEST2-HALCNRS