http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2002525376-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K1-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K7-64
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K1-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K1-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K7-64
filingDate 1999-09-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2002-08-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2002525376-A
titleOfInvention Auxiliary groups for amide bond formation
abstract (57) [Summary]nThe present invention relates to novel auxiliary groups for the formation of amide bonds and to the use of these auxiliary groups in various synthetic applications such as the synthesis of peptides and peptidomimetic compounds, in particular the "small cyclic peptides", so-called "difficulty". A new peptide group and a new auxiliary group for the synthesis of large peptides having a native peptide backbone. The auxiliary groups of the present invention are also useful as peptide synthesis for C-terminally modified peptides, on-resin cyclization of organic molecules, ligation chemistry, backbone substitution, and backbone linkers. In a particularly preferred embodiment, the present invention provides an auxiliary group that can be removed by photolysis. Synthetic methods for on-resin cyclization of linear or cyclic peptides, C-terminally modified peptides, or peptide molecules include the use of an amine nitrogen atom with an auxiliary compound of the present invention, a specific auxiliary compound (which may be (Which may be linked).
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2020529472-A
priorityDate 1998-09-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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