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Regioselective di- and tetra-functionalisation of γ-cyclodextrin using capping methodology.
| Content Provider | Semantic Scholar |
|---|---|
| Author | Jouffroy, Matthieu Armspach, Dominique Matt, Dominique Toupet, Loïc |
| Copyright Year | 2013 |
| Abstract | Alkylation of γ-cyclodextrin with 3 equiv. of 1,3-bis[bis(4-tert-butylphenyl)chloromethyl]benzene, followed by permethylation afforded selectively a singly capped (A,B), as well as two doubly capped (A,B:D,E and A,B:E,F) methylated γ-CDs. Deprotection with HBF4 gave quantitatively the corresponding diols and tetrols, which constitute valuable starting compounds for further functionalisation. |
| File Format | PDF HTM / HTML |
| DOI | 10.1039/c3ob40234g |
| PubMed reference number | 23624961 |
| Journal | Medline |
| Volume Number | 11 |
| Issue Number | 22 |
| Alternate Webpage(s) | http://www.rsc.org/suppdata/ob/c3/c3ob40234g/c3ob40234g.pdf |
| Alternate Webpage(s) | http://pdfs.semanticscholar.org/3f05/9faf49876e1c5f0542476ac6638a0a4e6438.pdf |
| Alternate Webpage(s) | https://doi.org/10.1039/c3ob40234g |
| Journal | Organic & biomolecular chemistry |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |