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Novabiochem Innovations
2008
Latest up-date: July. 2008
No. 1/08:
Overcoming aspartimide in Fmoc SPPS
No. 2/08:
Synthesis of β-amyloid using an isoacyl dipeptide
2007
No. 1/07: Synthesis of wild-type and phosphorylated phospholamban
No. 2/07: Synthesis of peptides containing methylated lysine residues
No. 3/07: Synthesis of the transmembrane region of bradykinin receptor
No. 4/07: Comparison of pseudoproline and isoacyl dipeptides in the synthesis of difficult peptides
No. 5/07
2006
No. 1/06: Synthesis of thymosin-α
1
using pseudoproline dipeptides.
No. 2/06: The role of HOBt in coupling reactions
No. 3/06: Synthesis of neurotoxic prion peptide (106 - 126)
No. 4/06: Smart peptide synthesis: Synthesis of PADRE-Muc chimeric peptide
No. 5/06: Synthesis of peptides containing arginine residues
No. 6/06: Smart peptide synthesis: Synthesis of the Rantes
2005
No. 1/05: New tools for the SPPS of FRET peptides.
No. 2/05: SPPS of biotinylated peptides.
No. 3/05: Synthesis of highly amyloidogenic human IAPP using pseudoproline dipeptides.
No. 4/05: New tools for SPPS of labeled peptides.
No. 5/05: Expediting convergent synthesis with pseudoproline dipeptides.
No. 6/05: Solid phase synthesis of AMC-based enzyme substrates.
2004
No. 1/04: Guidelines for the use of Pseudoproline Dipeptides
No. 2/04: Microwave accelerated Suzuki couplings employing a polymer-supported palladium phosphine
No. 3/04: Synthesis design using Pseudoproline Dipeptides
No. 4/04: Exploring strategies for peptide synthesis
No. 5/04: Strategies for the synthesis of peptide aldehydes
No. 6/04: Epimerization-free fragment condensation with
pseudoproline (oxazolidine) dipeptides.
2003
No. 1/03: New derivatives for overcoming aspartimide formation
No. 2/03: Synthesis of long peptides using pseudoproline dipeptides
No. 3/03: IBX Polystyrene
No. 4/03: Stability of polymer-supports to microwave heating
2002
No. 1/02: Immobilized T2/T2* triazenes: efficient tools for the synthesis of esters, amides, and guanidines
No. 2/02: Selenocysteine in native ligations and as a dehydroalanine precursor
No. 3/02: Polymer-supported alkylation reagents for the esterification of carboxylic acids
No. 4/02: Optimized coupling procedures for unusual amino acids
2001
No. 1/01: Reagent for the selective iodination of alkenes, alkynes and arenes
No. 2/01: Optimized protocols for the use of Fmoc-Dpr(ivDde)-OH
No. 3/01: Phosphopeptide synthesis using Fmoc-Tyr(PO(NMe2)2)-OH
No. 4/01: Optimized protocols for the addition of Fmoc-Aaa(PO(OBzl)OH)-OH
No. 5/01: Synthesis of amides using polymer-bound HOBt resin
2000
No. 2/00: Resin-bound thiophenol as SNAR-labile linkers
Synthesis of substituted arenes using mercaptophenyl resins by nucleophilic cleavage
No. 3/00: New resins for the SPOS of carboxamides and sulfonamides
Protocols for the use of formylindole resins in the synthesis of N-alkylcarboxamides and sulfonamides
No. 4/00: Polymer-supported oxidants for the conversion of primary alcohols
Protocols for the use of polymer-supported perruthenate
No. 5/00: Derivatives for the synthesis of difficult peptides
No. 6/00: Synthesis of peptide thioesters for chemoselective ligation
Protocols for the use of sulfamyl resins to prepare peptide thioesters
1999
No. 1/99: Orthogonally protected diamino acid derivatives
Protocols for selective removal of ivDde protecting group and the use of ivDde amino acids in SPPS
No. 2/99: Triazene-based resin for the traceless synthesis of arenes
Protocols for the preparation arenes and substituted arenes via immobilized triazenes prepared from diazonium compounds
No. 3/99: NovaGel resins
Use of PEG-PS NovaGel resins in SPPS
No. 4/99: Sulfonamide based safety-catch resins
Cleavage protocols for preparing peptide alkylamides and esters using sulfamyl-based resins
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©2008
Calbiochem
,
Novabiochem
, &
Novagen
are brands of EMD Chemicals Inc., an Affiliate of
Merck KGaA
, Darmstadt, Germany.