| Predicate |
Object |
| contentType |
Journal Article |
| endingPage |
8653 |
| issn |
0002-7863
1520-5126 |
| issueIdentifier |
28 |
| pageRange |
8652-8653 |
| publicationName |
Journal of the American Chemical Society |
| startingPage |
8652 |
| bibliographicCitation |
Yadav VK, Kumar NV. Highly stereoselective prins cyclization of silylmethyl-substituted cyclopropyl carbinols to 2,4,6-trisubstituted tetrahydropyrans. J Am Chem Soc. 2004 Jul 21;126(28):8652–3. doi: 10.1021/ja048000c. PMID: 15250708. |
| creator |
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_76e46d441e7abd44ea72a1f634cc4755
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_bdbc5ac554022dbe8b91071261b88b4c |
| date |
2004-06-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| identifier |
https://doi.org/10.1021/ja048000c
https://pubmed.ncbi.nlm.nih.gov/15250708 |
| isPartOf |
https://portal.issn.org/resource/ISSN/0002-7863
http://rdf.ncbi.nlm.nih.gov/pubchem/journal/4435
https://portal.issn.org/resource/ISSN/1520-5126 |
| language |
English |
| source |
https://www.crossref.org/
https://pubmed.ncbi.nlm.nih.gov/ |
| title |
Highly Stereoselective Prins Cyclization of Silylmethyl-Substituted Cyclopropyl Carbinols to 2,4,6-Trisubstituted Tetrahydropyrans |
| discussesAsDerivedByTextMining |
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_84e576a38922e4459d15cdc16b83f337
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID75644 |