(E)-4-(4-(tert-butyl)phenyl)but-3-en-1-ol
DOI: 10.14469/hpc/4151 Metadata
Created: 2018-05-10 15:56
Last modified: 2019-02-05 16:48
License: Creative Commons: Public Domain Dedication 1.0
Funding: (none given)
Co-author: Alan Spivey Co-author: Henry Rzepa
Description
Following the general procedure of synthesis of homoallylic alchols via Wittig olefination
Files
| Filename | Size | Type | Description |
|---|---|---|---|
| 1H.zip | 358KB | application/zip | Bruker 1H data |
| 1H.mnpub | 0 | chemical/x-mnpub | Mestrenova signature file for 1H.zip |
| 13C.zip | 374KB | application/zip | Bruker 13C data |
| 13C.mnpub | 0 | chemical/x-mnpub | Mestrenova signature file for 13C.zip |
| 1H+13C_assigned.mnova | 272KB | chemical/x-mnova | MestreNova data |
| 1H+13C_assigned.mnpub | 0 | chemical/x-mnpub | Mestrenova signature file for 1H+13C_assigned.mnova |
| MS.pdf | 7KB | application/pdf | MS |
| tBu_HA.cdxml | 5KB | chemical/x-cdxml | Chemdraw |
Member of collection / collaboration
| DOI | Description |
|---|---|
| 10.14469/hpc/3943 | FAIR Data: Reversibility and reactivity in an acid catalyzed cyclocondensation to give furanochromanes , a reaction at the oxonium-Prins vs. ortho-quinone methide cycloaddition mechanistic nexus |
Subject Keywords
| Keyword | Value |
|---|---|
| inchi | InChI=1S/C14H20O/c1-14(2,3)13-9-7-12(8-10-13)6-4-5-11-15/h4,6-10,15H,5,11H2,1-3H3/b6-4+ |
| inchikey | IVXXREZCAOVXSV-GQCTYLIASA-N |