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Angewandte Chemie International Edition, ISSN 1433-7851, 08/2011, Volume 50, Issue 33, pp. 7645 - 7649
Journal Article
Nature Protocols, ISSN 1754-2189, 2013, Volume 8, Issue 12, pp. 2483 - 2495
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 10/2012, Volume 51, Issue 41, pp. 10347 - 10350
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 09/2016, Volume 57, Issue 38, pp. 4264 - 4267
Peptide hydrazide ligation is a newly reported approach using C-terminus hydrazide as the precursor of thioester for ligation with N-terminus Cys-peptides.... 
C-terminus cyclization | Peptide hydrazide ligation | CTC-resin | SURROGATE | MECHANISM | SOLID-PHASE SYNTHESIS | NATIVE CHEMICAL LIGATION | CHEMISTRY | CHEMISTRY, ORGANIC | THIOESTERS | PROTEINS | Peptides | Glutamine
Journal Article
Organic Letters, ISSN 1523-7060, 03/2016, Volume 18, Issue 6, pp. 1222 - 1225
Journal Article
Organic and Biomolecular Chemistry, ISSN 1477-0520, 08/2014, Volume 12, Issue 29, pp. 5435 - 5441
Journal Article
Analytical Chemistry, ISSN 0003-2700, 11/2013, Volume 85, Issue 22, pp. 10670 - 10674
Journal Article
Journal Article
Organic and Biomolecular Chemistry, ISSN 1477-0520, 2018, Volume 16, Issue 10, pp. 1713 - 1719
A highly efficient sulfonylation of thiols has been achieved through the metal-free NaI/TBHP-mediated cross-coupling of sulfonyl hydrazides and thiols at room... 
THIOSULFONATE S-ESTERS | C(SP)-H BOND | ACIDS | BASE-CATALYZED OXIDATION | CHLORIDES | SULFONYLHYDRAZIDES | CHEMISTRY, ORGANIC | SULFENYLATION | PEPTIDE HYDRAZIDES | CHEMICAL-SYNTHESIS | ORGANIC DISULFIDES | Cross coupling | Thiols | Hydrazides | Metals | Functional groups
Journal Article
Organic & biomolecular chemistry, ISSN 1477-0520, 03/2018, Volume 16, Issue 10, pp. 1713 - 1719
A highly efficient sulfonylation of thiols has been achieved through the metal-free NaI/TBHP-mediated cross-coupling of sulfonyl hydrazides and thiols at room... 
Journal Article
Chemical Communications, ISSN 1359-7345, 2018, Volume 54, Issue 66, pp. 9127 - 9130
We report a simple and promising synthetic method to oxidize peptide hydrazides containing N-terminal thiazolidine as a protected cysteine. This yields the... 
TOXIN | NATIVE CHEMICAL LIGATION | CYSTEINE | DESULFURIZATION | CRAMBIN | PROTEIN-SYNTHESIS | CHEMISTRY, MULTIDISCIPLINARY | Synthesis | Thioesters | Hydrazides | Peptides
Journal Article
Tetrahedron, ISSN 0040-4020, 05/2014, Volume 70, Issue 18, pp. 2951 - 2955
The NY-ESO-1 (A39-A68) peptide hydrazide was prepared through 9-fluorenyl-methoxycarbonyl solid-phase peptide synthesis (Fmoc SPPS) from a new... 
Native chemical ligation | Peptide thioesters | Peptide hydrazides | Protein chemical synthesis | Fmoc hydrazine 2CTC resin | SAFETY-CATCH LINKER | CHEMISTRY, ORGANIC | S ACYL SHIFT | PROTEIN-SYNTHESIS | POLYPEPTIDES | Peptides | Hydrazines | Synthesis (chemistry) | Thioesters | Chlorides | Hydrazides | Resins | Polymers
Journal Article
Chemical Science, ISSN 2041-6520, 03/2017, Volume 8, Issue 4, pp. 3187 - 3191
The 1,3,4-oxadiazole is an aromatic heterocycle valued for its low-lipophilicity in drug development. Substituents at the 2- and/or 5-positions can modulate... 
Oxadiazoles | Synthesis | Amines | Reagents | Electronics | Amino acids | Hydrazides | Standards
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 11/2011, Volume 76, Issue 21, pp. 8756 - 8767
We have investigated the Z/E isomerism of the hydrazide link (CO-NH-N) and amidoxy link (CO-NH-O). The study was first focused on small molecular models using... 
TURNS | PEPTIDES | AZA-BETA-PEPTIDES | SOLID-PHASE SYNTHESIS | FOLDAMERS | CHEMISTRY, ORGANIC | BETA-PEPTOIDS | ACID OLIGOMERS | Amines - chemistry | Hydrazines - chemistry | Hydrogen Bonding | Magnetic Resonance Spectroscopy | Peptides - chemistry | X-Ray Diffraction | Molecular Conformation | Oxides - chemistry | Models, Molecular | Isomerism | Organic chemistry | Chemical Sciences
Journal Article
Chemical Science, ISSN 2041-6520, 2017, Volume 8, Issue 4, pp. 3187 - 3191
The 1,3,4-oxadiazole is an aromatic heterocycle valued for its low-lipophilicity in drug development. Substituents at the 2- and/or 5-positions can modulate... 
OXYGEN | ENANTIOSELECTIVE SYNTHESIS | UMPOLUNG AMIDE SYNTHESIS | ONE-POT SYNTHESIS | OXIDATIVE AMIDATION | ALDEHYDES | BROMONITROALKANES | PEPTIDE-SYNTHESIS | CHEMISTRY, MULTIDISCIPLINARY | CONJUGATE ADDITION | AMINE NUCLEOPHILES
Journal Article