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Sulfinimidate Esters as an Electrophilic Sulfinimidoyl Moti..:

Michael Andresini (5569343) ; Mauro Spennacchio (9315169) ; Marco Colella (4438567)...
https://figshare.com/articles/journal_contribution/Sulfinimidate_Esters_as_an_Electrophilic_Sulfinimidoyl_Motif_Source_Synthesis_of_i_N_i_Protected_Sulfilimines_from_Grignard_Reagents/16566000. , 2021

Link: https://doi.org/10.1021/acs.orglett.1c02413.s001

RT Journal
T1 <Title>Sulfinimidate Esters as an Electrophilic Sulfinimidoyl Motif Source: Synthesis of N ‑Protected Sulfilimines from Grignard Reagents</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_16566000&Exemplar=1&LAN=DE
				
A1 Michael Andresini (5569343)
A1 Mauro Spennacchio (9315169)
A1 Marco Colella (4438567)
A1 Gianluca Losito (11382261)
A1 Andrea Aramini (2478973)
A1 Leonardo Degennaro (1456936)
A1 Renzo Luisi (1360329)
YR 2021
K1 Biochemistry
K1 Medicine
K1 Genetics
K1 Molecular Biology
K1 Plant Biology
K1 Biological Sciences not elsewhere classified
K1 Chemical Sciences not elsewhere classified
K1 remarkable structural variability
K1 environmentally responsible conditions
K1 cyclopentyl methyl ether
K1 grignard reagents enables
K1 >‑ protected sulfilimines
K1 protected sulfilimines
K1 grignard reagents
K1 sulfinimidate esters
K1 n </
K1 high yields
K1 green solvent
K1 first time
JF https://figshare.com/articles/journal_contribution/Sulfinimidate_Esters_as_an_Electrophilic_Sulfinimidoyl_Motif_Source_Synthesis_of_i_N_i_Protected_Sulfilimines_from_Grignard_Reagents/16566000
LK http://dx.doi.org/https://doi.org/10.1021/acs.orglett.1c02413.s001
DO https://doi.org/10.1021/acs.orglett.1c02413.s001
SF ELIB - SuUB Bremen

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