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Alkenylation and Arylation of Peptides via Ni-Catalyzed Red..:

Xianghua Tao (11456895) ; Guobin Ma (1711423) ; Yanhong Song (4516555)...
https://figshare.com/articles/journal_contribution/Alkenylation_and_Arylation_of_Peptides_via_Ni-Catalyzed_Reductive_Coupling_of_i_C_i_Tosyl_Peptides_with_Csp_sup_2_sup_Triflates_Halides/16645773. , 2021

Link: https://doi.org/10.1021/acs.orglett.1c02601.s001

RT Journal
T1 <Title>Alkenylation and Arylation of Peptides via Ni-Catalyzed Reductive Coupling of α‑ C ‑Tosyl Peptides with Csp 2 Triflates/Halides</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_16645773&Exemplar=1&LAN=DE
				
A1 Xianghua Tao (11456895)
A1 Guobin Ma (1711423)
A1 Yanhong Song (4516555)
A1 Yunrong Chen (3945113)
A1 Qun Qian (576117)
A1 Deli Sun (6397298)
A1 Hegui Gong (1530778)
YR 2021
K1 Biophysics
K1 Biochemistry
K1 Molecular Biology
K1 Sociology
K1 Biological Sciences not elsewhere classified
K1 Chemical Sciences not elsewhere classified
K1 various unnatural di
K1 tripeptides containing vinyl
K1 catalyzed reductive cross
K1 aryl side chains
K1 catalyzed reductive coupling
K1 >‑ tosyl peptides
K1 2 </ sup
K1 peptides via ni
K1 tosyl peptides
K1 stage diversification
K1 protocol enables
K1 c </
JF https://figshare.com/articles/journal_contribution/Alkenylation_and_Arylation_of_Peptides_via_Ni-Catalyzed_Reductive_Coupling_of_i_C_i_Tosyl_Peptides_with_Csp_sup_2_sup_Triflates_Halides/16645773
LK http://dx.doi.org/https://doi.org/10.1021/acs.orglett.1c02601.s001
DO https://doi.org/10.1021/acs.orglett.1c02601.s001
SF ELIB - SuUB Bremen

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