Predicate |
Object |
assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_07c9542186133097bd6bbb7d92393090 |
classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2601-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B2200-07 |
classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C269-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C227-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C213-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D209-26 |
classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C269-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C271-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C217-64 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C215-28 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C213-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-26 |
filingDate |
2007-03-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate |
2010-10-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6efd4afd80b13359f3d4aed3cf4af553 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4659a9124403adb5e46271508686ee45 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e3c507947febb3127aa72b1b88614677 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3f3e94d6b6f8003d9741ad6ab37600b9 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_49078be98876a72ebf22bf65e59a8f6a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bbdf8a5b9358c2520ee43a88125bea46 |
publicationDate |
2010-10-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber |
US-7820858-B2 |
titleOfInvention |
Concise β2-amino acid synthesis via organocatalytic aminomethylation |
abstract |
The present invention provides a method for the synthesis of β 2 -amino acids. The method also provides methods yielding α-substituted β-amino aldehydes and β-substituted γ-amino alcohols. The present method according to this invention allows for increased yield and easier purification using minimal chromatography or crystallization. The methods described herein are based on an aldehyde aminomethylation which involves a Mannich reaction between an aldehyde and a formaldehyde-derived N,O-acetal (iminium precursor) and a catalyst, such as, for example, L-proline or a pyrrolidine. The invention allows for large scale, commercial preparation of β 2 -amino acids. |
priorityDate |
2006-03-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type |
http://data.epo.org/linked-data/def/patent/Publication |