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1
Published in 2020 at "ChemistryOpen"
DOI: 10.1002/open.202000178
Abstract: Abstract In the classical amidation between aromatic ketones and amines, 2.0 equivalents of amines are necessarily required to gain satisfying yields. The specific role of the amine in the direct amidation already puzzled us for…
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Keywords:
aromatic ketones;
amine direct;
direct amidation;
amine ... See more keywords
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1
Published in 2022 at "Journal of Peptide Science"
DOI: 10.1002/psc.3429
Abstract: Peptide‐bound methionine may transfer oxidative damage from the thioether side chain to the peptide backbone, catalyzing decomposition in general and α‐amidation in particular. In the present study, we focused on the reactivity and reaction pathways…
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Keywords:
amidation;
methionine;
directed amidation;
terminus directed ... See more keywords
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Published in 2022 at "Analytical and Bioanalytical Chemistry"
DOI: 10.1007/s00216-022-03894-y
Abstract: Spatial visualization of glycans within clinical tissue samples is critical for discovery of disease-relevant glycan dysregulations. Herein, we develop an on-tissue derivatization strategy for sensitive spatial visualization of N-glycans from formalin-fixed paraffin-embedded (FFPE) tissue sections,…
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Keywords:
tissue sections;
tissue;
sialic acid;
amidation ... See more keywords
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Published in 2018 at "Tetrahedron Letters"
DOI: 10.1016/j.tetlet.2018.11.036
Abstract: Abstract This is the first-time report on the repurposing n-butyl stannoic acid as a catalyst for direct amidation of carboxylic acids with amines. Notably, efficient amidation observed in comparison with all other catalytic methods reported…
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Keywords:
butyl stannoic;
catalyst direct;
stannoic acid;
repurposing butyl ... See more keywords
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Published in 2022 at "Bioconjugate chemistry"
DOI: 10.1021/acs.bioconjchem.2c00340
Abstract: Through a modified Kinugasa reaction, a novel method of amidation on terminal oligo alkyne conjugates by copper-promoted oxidation with nitrones has been developed. Unprotected bifunctional carboxylic acid-amine reagents can be transformed directly to the respective…
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Keywords:
amidation terminal;
dna compatible;
compatible oxidization;
terminal alkynes ... See more keywords
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1
Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.1c04265
Abstract: Methyltrimethoxysilane [MTM, CH3Si(OMe)3] has been demonstrated to be an effective, inexpensive, and safe reagent for the direct amidation of carboxylic acids with amines. Two simple workup procedures that provide the pure amide product without the…
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Keywords:
reagent direct;
direct amidation;
carboxylic acids;
amidation carboxylic ... See more keywords
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Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.1c04376
Abstract: Disclosed herein is a convenient Ir-catalyzed amidation of esters to access α-amido esters. Initially prepared silyl ketene acetals are directly employed, without separate purification, for subsequent amidation with an oxycarbonylnitrenoid precursor using the Cp*(LX)Ir(III) catalyst.…
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Keywords:
catalyzed amidation;
silyl ketene;
ketene acetals;
access ... See more keywords
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Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.2c01728
Abstract: The sturdy chelation of 1,2-diamines and transition-metals would retard or even interrupt the routine catalytic cycles. In the amidation and asymmetric reductive amination (ARA) cascade reactions of diamines and ketoesters, we deployed sets of additives…
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Keywords:
asymmetric reductive;
reductive amination;
amidation;
cascade reactions ... See more keywords
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Published in 2017 at "Organic letters"
DOI: 10.1021/acs.orglett.7b00583
Abstract: Cobalt(III) and rhodium(III) catalysts exhibited complementary scope in C-H amidation of aryl enaminones. The amidation reactions proceeded with broad scope under the assistance of a weakly coordinating and bifunctional enaminone directing group. The electrophilicity of…
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Keywords:
weakly coordinating;
enaminone;
iii rhodium;
cobalt iii ... See more keywords
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Published in 2017 at "Organic letters"
DOI: 10.1021/acs.orglett.7b02821
Abstract: Rh-catalyzed one-step reductive amidation of aldehydes has been developed. The protocol does not require an external hydrogen source and employs carbon monoxide as a deoxygenative agent. The direction of the reaction can be altered simply…
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Keywords:
dichotomy atom;
economical hydrogen;
atom economical;
amidation ... See more keywords
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Published in 2019 at "Organic letters"
DOI: 10.1021/acs.orglett.9b01732
Abstract: Cyclic sulfonamides (sultams) play a unique role in drug discovery and synthetic chemistry. A direct synthesis of sultams by an intramolecular C(sp3)-H amidation reaction using an iron complex in situ derived from Fe(ClO4)2 and aminopyridine…
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Keywords:
iron catalyzed;
synthesis sultams;
cyclic sulfonyl;
iron ... See more keywords