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Copper(I)-Catalyzed Asymmetric Synthesis of Unnatural α‑Ami..:

Zong-Ci Liu (11840444) ; Wen-Jun Yue (5932157) ; Liang Yin (458027)
https://figshare.com/articles/journal_contribution/Copper_I_-Catalyzed_Asymmetric_Synthesis_of_Unnatural_Amino_Acid_Derivatives_and_Related_Peptides_Containing_aza_Aryls/17207240. , 2021

Link: https://doi.org/10.1021/acs.joc.1c02426.s001

RT Journal
T1 <Title>Copper(I)-Catalyzed Asymmetric Synthesis of Unnatural α‑Amino Acid Derivatives and Related Peptides Containing γ‑(aza)Aryls</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_17207240&Exemplar=1&LAN=DE
				
A1 Zong-Ci Liu (11840444)
A1 Wen-Jun Yue (5932157)
A1 Liang Yin (458027)
YR 2021
K1 Biochemistry
K1 Molecular Biology
K1 Pharmacology
K1 Biotechnology
K1 Immunology
K1 Virology
K1 Chemical Sciences not elsewhere classified
K1 schiff bases derived
K1 corresponding chiral α
K1 catalytic asymmetric functionalization
K1 aryls chiral α
K1 high total yield
K1 amino acid derivatives
K1 high yields
K1 high enantioselectivity
K1 high diastereo
K1 well tolerated
K1 various azaarenes
K1 successfully applied
K1 present methodology
K1 organic chemistry
K1 nicely extended
K1 medicinal chemistry
K1 indispensable compounds
K1 finally afforded
K1 excellent enantioselectivities
K1 deficient butadienylpyridine
K1 deficient azaaryls
K1 deficient aryl
K1 benzo [<
K1 amino acids
K1 >] imidazole
K1 >- oxide
K1 >) ratio
K1 >) mixtures
JF https://figshare.com/articles/journal_contribution/Copper_I_-Catalyzed_Asymmetric_Synthesis_of_Unnatural_Amino_Acid_Derivatives_and_Related_Peptides_Containing_aza_Aryls/17207240
LK http://dx.doi.org/https://doi.org/10.1021/acs.joc.1c02426.s001
DO https://doi.org/10.1021/acs.joc.1c02426.s001
SF ELIB - SuUB Bremen

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