|
inhibitor |
6 |
|
s. aureus |
6 |
|
saer |
6 |
|
target |
6 |
|
virulence |
6 |
|
chemical protein synthesis |
5 |
|
amino acid |
4 |
|
carbanions |
4 |
|
chemical ligation |
4 |
|
decarboxylation |
4 |
|
density functional calculations |
4 |
|
native chemical ligation |
4 |
|
photochemistry |
4 |
|
radical ions |
4 |
|
serine/threonine ligation |
4 |
|
time‐resolved spectroscopy |
4 |
|
base-labile |
3 |
|
boc spps |
3 |
|
salicylaldehyde ester |
3 |
|
1,2-cis-glycosyl acetates |
2 |
|
acetates - chemical synthesis - chemistry |
2 |
|
acetylation |
2 |
|
acyl transfer |
2 |
|
amides - chemistry |
2 |
|
aminoalkylphosphonic acid |
2 |
|
aspartic acid ligation |
2 |
|
base-labile posttranslation modification |
2 |
|
carbohydrate conformation |
2 |
|
carrier protein |
2 |
|
chemoselectivity |
2 |
|
conjugation |
2 |
|
cyclic tetrapeptide |
2 |
|
cyclogentiotriose |
2 |
|
depsipeptide |
2 |
|
desulfurization |
2 |
|
deuteration |
2 |
|
drug conjugation |
2 |
|
galactosides - chemical synthesis - chemistry |
2 |
|
glucosides - chemical synthesis - chemistry |
2 |
|
glycoconjugates |
2 |
|
hmg proteins |
2 |
|
homogeneous protein conjugation |
2 |
|
hybrid molecule |
2 |
|
isoindoles |
2 |
|
isoindoles - chemical synthesis |
2 |
|
kaha ligation |
2 |
|
kinase assays |
2 |
|
lewis-acid catalyzed thioglycosylation |
2 |
|
macrocyclization |
2 |
|
mannich-type reaction |
2 |
|
molecular structure |
2 |
|
o-acetylation |
2 |
|
oligosaccharides |
2 |
|
ortho-phthalaldehyde |
2 |
|
peptide conjugation |
2 |
|
peptide cyclization |
2 |
|
peptide hydrazide |
2 |
|
peptides |
2 |
|
post-translational modifications |
2 |
|
protein synthesis |
2 |
|
radical desulfurization |
2 |
|
ring-chain tautomerization |
2 |
|
ring-closing glycosylation |
2 |
|
s-palmitoylation |
2 |
|
sdg3: good health and well-being |
2 |
|
selective oxidation |
2 |
|
ser/thr ligation |
2 |
|
site-specific protein modification |
2 |
|
sugar |
2 |
|
sulfhydryl compounds - chemistry |
2 |
|
synthesis |
2 |
|
thioglycoside |
2 |
|
vaccine |
2 |
|
β-selectivity |
2 |
|
alkenes |
1 |
|
alkylation |
1 |
|
alkylphosphonate |
1 |
|
amino acids |
1 |
|
asymmetric catalysis |
1 |
|
asymmetric reduction |
1 |
|
asymmetric synthesis |
1 |
|
bis(imidazoline)s |
1 |
|
bis(oxazoline) |
1 |
|
borane |
1 |
|
carboxyl polyether ionophores |
1 |
|
catalysis |
1 |
|
chemical biology |
1 |
|
chlorophosphite |
1 |
|
dbu |
1 |
|
dendrimers |
1 |
|
depsiphosphonopeptide |
1 |
|
dihydroacridine |
1 |
|
diphenylamine |
1 |
|
electronic effect |
1 |
|
enantioselectivity |
1 |
|
flexible scaffold |
1 |
|
friedel-crafts alkylation |
1 |
|
friedel-crafts reaction |
1 |
|
heterocycles |
1 |
|
homogeneous catalysis |
1 |
|
imidazoline |
1 |
|
imidazolines |
1 |
|
immobilization |
1 |
|
indoles |
1 |
|
ketone |
1 |
|
mass spectrometry |
1 |
|
michael addition |
1 |
|
multiple component condensation |
1 |
|
multiple-component condensation |
1 |
|
natural products |
1 |
|
nitroalkene |
1 |
|
nitroalkenes |
1 |
|
organic catalysis |
1 |
|
organocatalysis |
1 |
|
peptide |
1 |
|
phosphonopeptide |
1 |
|
pyrroles |
1 |
|
rigid scaffold |
1 |
|
substituent effects |
1 |
|
sulfonamides |
1 |
|
sulfur |
1 |
|
synthetic methods |
1 |
|
total synthesis |
1 |
