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Enantioselective Michael Addition/Cyclization/Desymmetrizat..:

Yu-Jie Li (3829312) ; Xue-Jiao Lv (6112556) ; Yan-Kai Liu (1396318)
https://figshare.com/articles/journal_contribution/Enantioselective_Michael_Addition_Cyclization_Desymmetrization_Sequence_of_Prochiral_Cyclic_Hemiacetals_and_Nitroolefins_Synthesis_of_Chiral_Oxygen-Bridged_Bicyclic_Compounds/21717880. , 2022

Link: https://doi.org/10.1021/acs.orglett.2c03815.s001

RT Journal
T1 <Title>Enantioselective Michael Addition/Cyclization/Desymmetrization Sequence of Prochiral Cyclic Hemiacetals and Nitroolefins: Synthesis of Chiral Oxygen-Bridged Bicyclic Compounds</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftunivfreestate:oai:figshare.com:article_21717880&Exemplar=1&LAN=DE
				
A1 Yu-Jie Li (3829312)
A1 Xue-Jiao Lv (6112556)
A1 Yan-Kai Liu (1396318)
YR 2022
K1 Biochemistry
K1 Medicine
K1 Cell Biology
K1 Physiology
K1 Computational Biology
K1 Environmental Sciences not elsewhere classified
K1 Biological Sciences not elsewhere classified
K1 prochiral cyclic hemiacetals
K1 hydrogen bond catalysis
K1 experimental results suggest
K1 enantioselective michael addition
K1 bridged bicyclic compounds
K1 subsequent diastereocontrolled cyclization
K1 1 ] nonane
K1 desymmetrization divergent process
K1 desymmetrization process
K1 desymmetrization sequence
K1 cooperative enamine
K1 chiral oxygen
JF https://figshare.com/articles/journal_contribution/Enantioselective_Michael_Addition_Cyclization_Desymmetrization_Sequence_of_Prochiral_Cyclic_Hemiacetals_and_Nitroolefins_Synthesis_of_Chiral_Oxygen-Bridged_Bicyclic_Compounds/21717880
LK http://dx.doi.org/https://doi.org/10.1021/acs.orglett.2c03815.s001
DO https://doi.org/10.1021/acs.orglett.2c03815.s001
SF ELIB - SuUB Bremen

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