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hydrazinopeptides (17) 17
peptides (11) 11
chemistry, organic (7) 7
chemical ligation (6) 6
chemical sciences (5) 5
hydrazines - chemical synthesis (5) 5
peptides - chemistry (5) 5
amination (4) 4
amino acid sequence (4) 4
hydrazines - chemistry (4) 4
hydrazinoturn (4) 4
index medicus (4) 4
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[chim]chemical sciences (3) 3
acids (3) 3
acylation (3) 3
aim (3) 3
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biochemistry & molecular biology (3) 3
electrophilic amination (3) 3
hydrazinopeptide (3) 3
n-electrophilic amination (3) 3
n‐electrophilic amination (3) 3
organic chemistry (3) 3
peptides - chemical synthesis (3) 3
proteins (3) 3
pseudopeptide (3) 3
solid-phase synthesis (3) 3
[chim.orga]chemical sciences/organic chemistry (2) 2
amino-acids (2) 2
aza-beta-peptides (2) 2
biochemical research methods (2) 2
chemistry, medicinal (2) 2
chemistry, multidisciplinary (2) 2
chemistry, organic - methods (2) 2
cleavage step (2) 2
crystallography, x-ray (2) 2
derivatives (2) 2
design (2) 2
dianisylpeptides (2) 2
esters (2) 2
fluorenes - chemistry (2) 2
foldamers (2) 2
high optical purity (2) 2
hofmann‐type elimination (2) 2
humans (2) 2
hydrazone (2) 2
life sciences (2) 2
ligand (2) 2
magnetic resonance spectroscopy (2) 2
organic compounds (2) 2
peptidomimetics (2) 2
protein conformation (2) 2
research (2) 2
solid‐phase synthesis (2) 2
stereoisomerism (2) 2
synthesis (2) 2
time-resolved fret (2) 2
1,3,4-oxadiazolidine (1) 1
1,3,4-oxadizaolidine (1) 1
1,3,4‐oxadiazolidine (1) 1
1:1 [alpha/alpha-n-alpha-hydrazino]mers (1) 1
1:1 [α/α-n (1) 1
1:1 [α/α-nα-hydrazino]mers (1) 1
2 (1) 1
2-a]quinoxalines (1) 1
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[chim.theo]chemical sciences/theoretical and/or physical chemistry (1) 1
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Tetrahedron, ISSN 0040-4020, 06/2012, Volume 68, Issue 24, pp. 4682 - 4692
Different α-hydrazinoesters with high optical purity have been obtained in large scale via an SN2 protocol. A coupling reaction with a natural amino acid leads... 
Hydrazinoturn | 1:1 [α/α-Nα-Hydrazino]mers | α-Hydrazinoester | SN2 | Hydrazinopeptide | Pseudopeptide | 1:1 [α/α-N | 2 | S | Hydrazino]mers | DESIGN | alpha-Hydrazinoester | 1:1 [alpha/alpha-N-alpha-Hydrazino]mers | S(N)2 | STABILITY | CHEMISTRY, ORGANIC | PEPTIDES | AZA-BETA-PEPTIDES | HYDRAZINOACIDS | FOLDAMERS | AMINOXY ACIDS
Journal Article
Journal Article
ChemMedChem, ISSN 1860-7179, 06/2017, Volume 12, Issue 12, pp. 940 - 953
Journal Article
Tetrahedron, ISSN 0040-4020, 2007, Volume 63, Issue 10, pp. 2223 - 2234
The preparation of chiral orthogonally protected N α-Z, N β-Fmoc- or Boc-α-hydrazinoacids derivatives, directly suitable for SPPS, is described in six steps... 
Protecting group | α-Hydrazinodipeptide | α-Hydrazinoacid | Mitsunobu reaction | Pseudopeptide | alpha-hydrazinodipeptide | ASYMMETRIC-SYNTHESIS | REAGENTS | STEREOSELECTIVE AMINATION | CHEMISTRY, ORGANIC | ELECTROPHILIC AMINATION | AMINO-ACID FLUORIDES | HIGH OPTICAL PURITY | pseudopeptide | PEPTIDES | alpha-hydrazinoacid | ESTERS | HYDRAZINOPEPTIDES | protecting group | DERIVATIVES
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 2000, Volume 41, Issue 1, pp. 45 - 48
N-terminal α-hydrazinoacetylpeptides were synthesized and chemoselectively acylated on the hydrazine moiety with various fatty acid succinimidyl esters or... 
hydrazinopeptide | α-hydrazinoacetyl | lipopeptide | fatty acids | acylation | α-Hydrazinoacetyl | Fatty acids | Hydrazinopeptide | Lipopeptide | Acylation | alpha-hydrazinoacetyl | CHEMISTRY, ORGANIC | MODEL
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 06/2001, Volume 66, Issue 12, pp. 4153 - 4160
A novel linker, based on the anchoring of (+)-dimethyl 2,3-O-isopropylidene-d-tartrate to PEGA or PEG-PS solid supports, was developed for the solid-phase... 
AMINATION | SERINE | UNPROTECTED PEPTIDES | TRANSCRIPTION | CHEMISTRY | CHEMISTRY, ORGANIC | CHEMICAL LIGATION | HYDRAZINOPEPTIDES | PROTEINS | WATER | Chromatography, High Pressure Liquid | Oxidation-Reduction | Peptides - chemistry | Tartrates - chemistry | Aldehydes - chemical synthesis | Gums and resins | Usage | Synthesis | Peptides | Organic compounds | Organic chemistry | Chemical Sciences
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 1999, Volume 40, Issue 8, pp. 1491 - 1494
The N-alkyl hydrazino group of hydrazinopeptides 1 is oxidized by air in bicarbonate buffers into the corresponding hydroperoxy moiety in high yield. The... 
hydrazinopeptides/ N-electrophilic amination/hydroperoxydeamination | Hydroperoxydeamination | N-electrophilic amination | Hydrazinopeptides | CHEMISTRY, ORGANIC | hydrazinopeptides | HYDROPEROXIDES | hydroperoxydeamination
Journal Article
Journal of Molecular Structure: THEOCHEM, ISSN 0166-1280, 11/2008, Volume 869, Issue 1-3, pp. 41 - 46
This paper follows a previous publication [Salaün, A., et al., Conformation of Nα-substituted hydrazino acetamides in CDCl , the precious help of the analysis... 
Aza-β | Hydrazinoturn | peptides | Bifurcated hydrogen bonding | AIM | Hydrazinopeptides
Journal Article
Journal of Molecular Structure: THEOCHEM, ISSN 0166-1280, 2008, Volume 869, Issue 1, pp. 41 - 46
This paper follows a previous publication [Salaün, A., et al., Conformation of Nα-substituted hydrazino acetamides in CDCl 3, the precious help of the analysis... 
Hydrazinoturn | Bifurcated hydrogen bonding | Aza-β 3-peptides | AIM | Hydrazinopeptides
Journal Article
07/2012, ISBN 3527330437, 37
This chapter contains sections titled: Introduction Hydroxylamine Components in the Ugi Reaction Hydrazine Components in the Ugi Reaction Miscellaneous Amine... 
amine surrogates | isocyanides | ring‐forming processes | Multicomponent reactions | Ugi reaction | atom economy | peptidomimetics | post‐Ugi modifications | hydrazinopeptides | intramolecular reactions | Post-Ugi modifications | Peptidomimetics | Hydrazinopeptides | Ring-forming processes | Intramolecular reactions | Amine surrogates | Isocyanides | Atom economy
Book Chapter
JOURNAL OF MOLECULAR STRUCTURE-THEOCHEM, ISSN 0166-1280, 11/2008, Volume 869, Issue 1-3, pp. 41 - 46
Journal Article
Journal of Peptide Research, ISSN 1397-002X, 10/1999, Volume 54, Issue 4, pp. 270 - 278
: The synthesis of hydrazinopeptides using solid‐phase N‐electrophilic amination was extended to the Fmoc/tert‐butyl strategy. Both Boc/benzyl and... 
cleavage step | N‐electrophilic amination | dianisylpeptides | Hofmann‐type elimination | hydrazinopeptides | solid‐phase synthesis
Journal Article
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