Rappe Rearrangement. Bicyclooxirane formation, final opening retro 2+2, TS4, OH...Br H bond, trans, Def2-SVPP, G = -2880.032364
DOI: 10.14469/hpc/10894 Metadata
Created: 2022-08-17 06:52
Last modified: 2025-03-27 14:17
License: Creative Commons: Public Domain Dedication 1.0
Funding: (none given)
Description
Gaussian 16 (C01) calculation
Files
| Filename | Size | Type | Description |
|---|---|---|---|
| Rappe3-8-3-2.gjf | 996 | chemical/x-gaussian-input | Gaussian input file |
| Rappe3-8-3-2.log | 727KB | chemical/x-gaussian-log | Gaussian log file |
| checkpoint.fchk | 844KB | chemical/x-gaussian-checkpoint | Formatted checkpoint file |
| opt.cml | 1KB | chemical/x-cml | Optimised geometry |
Member of collection / collaboration
| DOI | Description |
|---|---|
| 10.14469/hpc/11044 | The Rappe Rearrangement. The origin of cis-stereoselectivity in the conversion of 2,3-dibromo-2-methyl-cyclopropan-1-one to (Z)-but-2-enoic acid. TS3 and TS4 pathways |
Subject Keywords
| Keyword | Value |
|---|---|
| Gibbs_Energy | -2880.032364 |
| inchi | InChI=1S/C4H6O2.Br/c1-3-2-4(3,5)6;/h2-3,5H,1H3;/t3-,4+;/m0./s1 |
| inchikey | DRQLWZQTXDGOIW-RFKZQXLXSA-N |