| Predicate |
Object |
| contentType |
Journal Article |
| endingPage |
284 |
| issn |
1861-471X
1861-4728 |
| issueIdentifier |
2 |
| pageRange |
272-284 |
| publicationName |
Chemistry – An Asian Journal |
| startingPage |
272 |
| bibliographicCitation |
Stadler D, Bach T. Highly diastereoselective Friedel-Crafts alkylation reactions via chiral alpha-functionalized benzylic carbocations. Chem Asian J. 2008 Feb 01;3(2):272–84. doi: 10.1002/asia.200700241. PMID: 17985329. |
| creator |
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_48bc77d0c98e87e3027be124a6c76088
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_f5f1faa7be454331b45feb5533b19de0
http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-1342-0202 |
| date |
2008-01-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| identifier |
https://doi.org/10.1002/asia.200700241
https://pubmed.ncbi.nlm.nih.gov/17985329 |
| isPartOf |
https://portal.issn.org/resource/ISSN/1861-471X
https://portal.issn.org/resource/ISSN/1861-4728
http://rdf.ncbi.nlm.nih.gov/pubchem/journal/33302 |
| language |
English |
| source |
https://pubmed.ncbi.nlm.nih.gov/
https://www.crossref.org/ |
| title |
Highly diastereoselective Friedel-Crafts alkylation reactions via chiral alpha-functionalized benzylic carbocations |
| discussesAsDerivedByTextMining |
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID961
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5975
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11126
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID313 |