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Haloamines as Bifunctional Reagents for Oxidative Aminohalo..:

Xueying Zhou (320107) ; Yujing Yao (5907578) ; Caihong Wang (535816)...
https://figshare.com/articles/journal_contribution/Haloamines_as_Bifunctional_Reagents_for_Oxidative_Aminohalogenation_of_Maleimides/14404550. , 2021

Link: https://doi.org/10.1021/acs.orglett.1c01052.s001

RT Journal
T1 <Title>Haloamines as Bifunctional Reagents for Oxidative Aminohalogenation of Maleimides</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_14404550&Exemplar=1&LAN=DE
				
A1 Xueying Zhou (320107)
A1 Yujing Yao (5907578)
A1 Caihong Wang (535816)
A1 Yaling Xu (8055806)
A1 Wenliang Zhang (50782)
A1 Yunfei Ma (1777753)
A1 Ge Wu (1897054)
YR 2021
K1 Biochemistry
K1 Microbiology
K1 Genetics
K1 Biotechnology
K1 Developmental Biology
K1 Inorganic Chemistry
K1 Environmental Sciences not elsewhere classified
K1 Chemical Sciences not elsewhere classified
K1 Bifunctional Reagents
K1 umpolung
K1 copper-catalyzed oxidative aminohal
K1 alkene aminoiodination
K1 multicomponent reaction
K1 late-stage modification
K1 Br
K1 amines
K1 NXS
K1 iodoamine
K1 drug molecules
K1 difunctionalized reagents
K1 Haloamine
K1 formation
K1 cascade strategy exploits
K1 Cl
K1 Oxidative Aminohalogenation
K1 Maleimide
K1 substrate range
K1 bond
K1 electron-deficient maleimides
JF https://figshare.com/articles/journal_contribution/Haloamines_as_Bifunctional_Reagents_for_Oxidative_Aminohalogenation_of_Maleimides/14404550
LK http://dx.doi.org/https://doi.org/10.1021/acs.orglett.1c01052.s001
DO https://doi.org/10.1021/acs.orglett.1c01052.s001
SF ELIB - SuUB Bremen

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