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filingDate 1992-07-15^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1994-04-19^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_84422ff70f8279a366c9353ec2f680f1
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publicationDate 1994-04-19^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5304497-A
titleOfInvention Method of forming N-protected amino acid thiohydantoins
abstract A method of forming a thiohydantoin from an N-protected amino acid. The method employs a uronium or phosphonium compound to activate the terminal carboxyl group of the amino acid and a thiocyanate reagent to cyclize the activated amino acid to the thio-hydantoin. The thiohydantoin can be cleaved from its N-protecting group, for use in C-terminal peptide sequencing. Particularly preferred uronium compounds include salts of 2-chlorouronium. Preferred thiocyanate reagents include trimethylsilyl isothiocyanate and crown ether adducts of metallothiocyanates, such as the 18-crown-6 adduct of KSCN.
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