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1 Ergebnisse
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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
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
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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