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Evaluation of Cyclic Amides as Activating Groups in N–C Bon..:

Md. Mahbubur Rahman (4068862) ; Daniel J. Pyle (11149197) ; Elwira Bisz (4900105)...
https://figshare.com/articles/journal_contribution/Evaluation_of_Cyclic_Amides_as_Activating_Groups_in_N_C_Bond_Cross-Coupling_Discovery_of_i_N_i_Acyl-_-valerolactams_as_Effective_Twisted_Amide_Precursors_for_Cross-Coupling_Reactions/14999403. , 1753

Link: https://doi.org/10.1021/acs.joc.1c01110.s001

RT Journal
T1 <Title>Evaluation of Cyclic Amides as Activating Groups in N–C Bond Cross-Coupling: Discovery of N ‑Acyl-δ-valerolactams as Effective Twisted Amide Precursors for Cross-Coupling Reactions</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_14999403&Exemplar=1&LAN=DE
				
A1 Md. Mahbubur Rahman (4068862)
A1 Daniel J. Pyle (11149197)
A1 Elwira Bisz (4900105)
A1 Błażej Dziuk (4900111)
A1 Krzysztof Ejsmont (1726204)
A1 Roger Lalancette (1581853)
A1 Qi Wang (22418)
A1 Hao Chen (5190)
A1 Roman Szostak (1545610)
A1 Michal Szostak (1305681)
YR 1753
K1 Biochemistry
K1 Medicine
K1 Cell Biology
K1 Molecular Biology
K1 Physiology
K1 Chemical Sciences not elsewhere classified
K1 cross-coupling reactions
K1 reactivity order
K1 model N
K1 Cyclic Amides
K1 Computational studies
K1 acyl-activated amide precursors
K1 amidic resonance
K1 N-activating groups
K1 amide bond
K1 Effective Twisted Amide Precursors
K1 unreactive amide bonds
K1 amide electrophiles
K1 reaction conditions
K1 phenolic esters
K1 medium distortion range
K1 acyl -δ-valerolactam
K1 X-ray structure
K1 six-membered rings
K1 acyl -δ-valerolactams
K1 Activating Groups
JF https://figshare.com/articles/journal_contribution/Evaluation_of_Cyclic_Amides_as_Activating_Groups_in_N_C_Bond_Cross-Coupling_Discovery_of_i_N_i_Acyl-_-valerolactams_as_Effective_Twisted_Amide_Precursors_for_Cross-Coupling_Reactions/14999403
LK http://dx.doi.org/https://doi.org/10.1021/acs.joc.1c01110.s001
DO https://doi.org/10.1021/acs.joc.1c01110.s001
SF ELIB - SuUB Bremen

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