86359
TentaGel™ S-NH2
extent of labeling: 0.20-0.35 mmol/g N loading
Synonym(s):
O-(2-Aminoethyl)polyethylene glycol polymer-bound
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About This Item
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product line
TentaGel™
Quality Level
form
solid
reaction suitability
reaction type: Fmoc solid-phase peptide synthesis
extent of labeling
0.20-0.35 mmol/g N loading
particle size
110-150 μm
application(s)
peptide synthesis
functional group
amine
storage temp.
2-8°C
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Application
TentaGel™ S-NH2 can be used:
- As a support in the synthesis of L-Leu based peptides and oligomers, which are used as catalysts in Julia-Colonna epoxidation of chalcones.
- In the synthesis of 1,3-dialkyl quinazoline-2,4-diones.
- To synthesize N-substituted amidinoaryloxypyridine analogs as potent factor Xa inhibitors.
Legal Information
TentaGel is a trademark of Rapp Polymere GmbH
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Highly enantioselective enone epoxidation catalyzed by short solid phase-bound peptides: dominant role of peptide helicity
Berkessel A, et al.
Organic Letters, 3(24), 3839-3842 (2001)
Solid-phase synthesis of 1, 3-dialkyl quinazoline-2, 4-diones
Buckman BO and Mohan R
Tetrahedron Letters, 37(26), 4439-4442 (1996)
Solid-phase synthesis of N-substituted amidinophenoxy pyridines as factor Xa inhibitors
Mohan R, et al.
Bioorganic & Medicinal Chemistry Letters, 8(14), 1877-1882 (1998)
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