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Synthesis of 4‑Selenothreofuranose Derivatives via Pummerer..:

Michio Iwaoka (1589773) ; Yuta Hiyoshi (11028367) ; Shota Arai (5158784).
https://figshare.com/articles/dataset/Synthesis_of_4_Selenothreofuranose_Derivatives_via_Pummerer-Type_Reactions_of_i_trans_i_-3_4-Dioxygenated_Tetrahydroselenophenes_Mediated_by_a_Selenonium_Intermediate/14850079. , 1753

Link: https://doi.org/10.1021/acsomega.1c02160.s002

RT Journal
T1 <Title>Synthesis of 4‑Selenothreofuranose Derivatives via Pummerer-Type Reactions of trans -3,4-Dioxygenated Tetrahydroselenophenes Mediated by a Selenonium Intermediate</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_14850079&Exemplar=1&LAN=DE
				
A1 Michio Iwaoka (1589773)
A1 Yuta Hiyoshi (11028367)
A1 Shota Arai (5158784)
A1 Takeru Ito (2324605)
YR 1753
K1 Biochemistry
K1 Medicine
K1 Molecular Biology
K1 Evolutionary Biology
K1 Plant Biology
K1 Virology
K1 Computational Biology
K1 Chemical Sciences not elsewhere classified
K1 BF
K1 4- selenotherofuranose derivatives
K1 anomeric carbon atom decreases
K1 latter glycosylation reaction
K1 tran
K1 1 H NMR spectroscopy
K1 Selenonium Intermediate Selenosugars
K1 selectivity
K1 anomeric position
K1 selenosugar
K1 racemic 4- selenothreofuranose deri
K1 seleno-Pummerer rearrangement
JF https://figshare.com/articles/dataset/Synthesis_of_4_Selenothreofuranose_Derivatives_via_Pummerer-Type_Reactions_of_i_trans_i_-3_4-Dioxygenated_Tetrahydroselenophenes_Mediated_by_a_Selenonium_Intermediate/14850079
LK http://dx.doi.org/https://doi.org/10.1021/acsomega.1c02160.s002
DO https://doi.org/10.1021/acsomega.1c02160.s002
SF ELIB - SuUB Bremen

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