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Synthesis of 1,2,4-Oxadiazolines through Deoxygenative Cycl..:

Cai-Mei Nong (14310809) ; Si-Ning Lv (14310812) ; Wei-Min Shi (1490176)...
https://figshare.com/articles/journal_contribution/Synthesis_of_1_2_4-Oxadiazolines_through_Deoxygenative_Cyclization_of_i_N_i_Vinyl-_-Unsaturated_Nitrones_with_i_in_Situ_i_Generated_Nitrile_Oxides_from_Hydroxamoyl_Chlorides/21792719. , 2022

Link: https://doi.org/10.1021/acs.orglett.2c04121.s001

RT Journal
T1 <Title>Synthesis of 1,2,4-Oxadiazolines through Deoxygenative Cyclization of N ‑Vinyl-α,β-Unsaturated Nitrones with in Situ Generated Nitrile Oxides from Hydroxamoyl Chlorides</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftunivfreestate:oai:figshare.com:article_21792719&Exemplar=1&LAN=DE
				
A1 Cai-Mei Nong (14310809)
A1 Si-Ning Lv (14310812)
A1 Wei-Min Shi (1490176)
A1 Cui Liang (116477)
A1 Gui-Fa Su (1490179)
A1 Dong-Liang Mo (1490182)
YR 2022
K1 Biochemistry
K1 Microbiology
K1 Cell Biology
K1 Genetics
K1 Molecular Biology
K1 Developmental Biology
K1 Marine Biology
K1 Virology
K1 Computational Biology
K1 Environmental Sciences not elsewhere classified
K1 Chemical Sciences not elsewhere classified
K1 mechanistic studies revealed
K1 generated nitrile oxides
K1 3 ]- rearrangement
K1 nitrile oxides
K1 unsaturated nitrones
K1 thermal conditions
K1 situ </
K1 sequential elimination
K1 proh solvent
K1 polysubstituted pyrroles
K1 oxadiazoline derivatives
K1 n </
K1 major products
K1 intramolecular cyclization
K1 hydroxamoyl chlorides
K1 good yields
K1 easily converted
K1 deoxygenative cyclization
K1 also obtained
K1 >‑ vinyl
K1 >- vinyl
JF https://figshare.com/articles/journal_contribution/Synthesis_of_1_2_4-Oxadiazolines_through_Deoxygenative_Cyclization_of_i_N_i_Vinyl-_-Unsaturated_Nitrones_with_i_in_Situ_i_Generated_Nitrile_Oxides_from_Hydroxamoyl_Chlorides/21792719
LK http://dx.doi.org/https://doi.org/10.1021/acs.orglett.2c04121.s001
DO https://doi.org/10.1021/acs.orglett.2c04121.s001
SF ELIB - SuUB Bremen

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