http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1458729-B1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_37f4922dfb7777b019e504b885211b8e http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_9c37762188a56acca3ecbc14acf8881b |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F5-02 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F5-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00 |
| filingDate | 2002-12-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2006-03-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aeb79dcbed7c2a198d99d2896e59d644 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c8c36ca7014465ad1da4f9fc59b0aa6e http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5a4ef77c45a4438922cca1dde6d18d54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_97effa7c5934f5146877191f660cc5a2 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_48d84134b535ed97285a0f6434a3824d |
| publicationDate | 2006-03-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | EP-1458729-B1 |
| titleOfInvention | (aryl) (amino) borane compounds, method for preparing same |
| abstract | Aminoborane derivatives (I) are new. Compounds of formula (I) are new: A-BH-NR<1>R<2> (I) R<1>, R<2> = 2-20C alkyl, 3-20C cycloalkyl or aralkyl, or R<1>+R<2> is alkylene, and preferably the groups are chiral; A = aryl, heteroaryl, vinyl, dienyl, polyenyl or alkynyl, all optionally substituted with alkyl, alkoxy, amino, dialkylamino, halo, CN, ester, amide, (thio)acetal, (thio)ketal, trialkylsilyl and dialkoxyboryl. Independent claims are also included for: (i) a process for preparing compounds (I); (ii) production of arylboratranes by reacting (I) with dihydroxyethylamines; (iii) production of 2-aryl-5,5-dimethyl-1,3,2-dioxaborinanes by reacting (I) with 2,2-dimethyl-1,4-propanediol; (iv) production of arylboronic acids by reaction (I) with excess methanol and hydrolyzing the resulting aryldimethoxyborane; (v) production of B,B-diaryl-aminoboranes by reacting (I) with A-X (not defined) in the presence of a zero-valent palladium (Pd(0)) catalyst and a base; (vi) production of compounds A-A by reacting (I) with A-Z (not defined) in the presence of a Pd(0) catalyst, a base and water. |
| priorityDate | 2001-12-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 77.