Paper
1H-Benzotriazol-1-yl methanesulfonate: A regioselective N-mesylating reagent
Published 1999 · Sun Young Kim, N. Sung, Joong-Kwon Choi
Tetrahedron Letters
Q3 SJR score
12
Citations
0
Influential Citations
Abstract
Abstract hidden due to publisher request; this does not indicate any issues with the research. Click the full text link above to read the abstract and view the original source.
Study Snapshot
1H-Benzotriazol-1-yl methanesulfonate effectively performs selective mesylation for differentiating amino groups, allowing for easier identification of compounds with both amino and hydroxy groups.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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References
Synthesis of Pyrazoloquinolines as Gastric H+/K+-ATPase Inhibitors.
Pyrazoloquinolines show potential as anti-ulcer agents by inhibiting gastric H+/K+-ATPase, with regiospecific synthesis achieved.
2010·5citations·G. Kalayanov et al.·ChemInform
ChemInform
A Facile Method for Direct Conversion of Dihydrofuroquinolones to Dihydropyrroloquinolones.
This study presents a novel and efficient method for one-step conversion of dihydrofuroquinolones to dihydropyrroloquinolones in high yields under mild conditions, potentially benefiting therapeutic applications in peptic ulcer and gastroesophageal reflux disease treatment.
1998·16citations·Sungsoo S. Kim et al.·ChemInform
ChemInform
A facile synthesis of 2,3-disubstituted pyrrolo[2,3-b]pyridines via palladium-catalyzed heteroannulation with internal alkynes
Palladium-catalyzed heteroannulation with internal alkynes allows for the facile synthesis of 2,3-disubstituted pyrrolo[2,3-b]pyridines.
1998·79citations·Sang Sun Park et al.·Tetrahedron Letters
Tetrahedron Letters
Nosylaziridines: Activated aziridine electrophiles
Nosylaziridines are highly reactive electrophiles that produce S n 2 adducts, which can be easily cleaved to provide primary amines under mild conditions.
1997·84citations·P. Maligres et al.·Tetrahedron Letters
Tetrahedron Letters
6-Nitro-1-β-napthalenesulfonyloxybenzotriazole : A novel coupling reagent for peptide synthesis
N-NSBt is a novel coupling reagent for rapid and quantitative peptide synthesis in a stepwise manner.
1993·12citations·B. Devadas et al.·Tetrahedron Letters
Tetrahedron Letters
Peptides. VII. Some sulfonates of strongly acidic N-hydroxy compounds as novel coupling reagents.
Sulfonates of strongly acidic N-hydroxy compounds are excellent coupling reagents for amide bond formation, enabling the preparation of various active esters and protected di- and tripeptides.
1974·21citations·M. Itoh et al.·Bulletin of the Chemical Society of Japan
Bulletin of the Chemical Society of Japan
Citations
Synthesis, structure, theoretical calculations and biological activity of sulfonate active ester new derivatives
New sulfonate esters derivatives show promising antimicrobial activity against human cancer cell lines and mosquito larvae.
2013·8citations·Mohamed Ghazzali et al.·Journal of Molecular Structure
Journal of Molecular Structure
Peptide coupling reagents, more than a letter soup.
Peptide coupling reagents offer a versatile tool for synthesis of complex molecules, enabling applications in biomedicine, bioengineering, and nanomedicine.
2011·833citations·A. El‐Faham et al.·Chemical reviews
Chemical reviews
N‐Hydroxylamines for Peptide Synthesis
N-hydroxylamines are essential additives for peptide synthesis, aiding in the synthesis of phosphonium, uronium/iminium salts, active esters, phosphate and sulfonate coupling reagents, and polymer bond N-hydroxylamine
2010·6citations·Ramon Subirós‐Funosas et al.·Patai's Chemistry of Functional Groups
Patai's Chemistry of Functional Groups
Alkyl Chalcogenides: Sulfur‐Based Functional Groups
Novel methods for preparing sulfur-based compounds, including chiral syntheses, are reviewed for eco-friendly organic synthesis and biological applications.
2005·6citations·I. Shcherbakova et al.·ChemInform
ChemInform
Differentially-protected steroidal triamines; scaffolds with potential for medicinal, supramolecular, and combinatorial chemistry.
Differentially-protected triamino scaffolds, 13 and 14, show potential for medicinal, supramolecular, and combinatorial chemistry, with high steric hindrance sensitivity and high yield from cholic acid.
2004·48citations·V. D. Amo et al.·Organic & biomolecular chemistry
Organic & biomolecular chemistry
Microwave‐Induced Rapid Access to Aromatic and Heteroaromatic Sulfonamides Under Solvent‐Free Conditions Without Using External Base
Microwave-induced syntheses of sulfonamides under solvent-free conditions provide fast, simple, and customizable access to aromatic and heteroaromatic sulfonamides without using external base.
2004·7citations·Ashwani Sharma et al.·Synthetic Communications
Synthetic Communications
PENTAFLUOROPHENYL 4-NITROBENZENESULFONATE AS A PEPTIDE COUPLING REAGENT
PFNB effectively couples Boc- or Fmoc-protected amino acids with amino acid esters, resulting in high yields of protected dipeptides.
2001·6citations·K. Pudhom et al.·Synthetic Communications
Synthetic Communications