Rappe Rearrangement. BicycloOxirane formation, Sn2, cis, GS for TS2/3, 4H2O.Na, Def2-SVPP, G = -3347.581100
DOI: 10.14469/hpc/11188 Metadata
Created: 2022-09-21 17:12
Last modified: 2025-03-27 14:14
License: Creative Commons: Public Domain Dedication 1.0
Funding: (none given)
Description
Gaussian 16 (C01) calculation
Files
| Filename | Size | Type | Description |
|---|---|---|---|
| Rappe3-9-2.gjf | 1KB | chemical/x-gaussian-input | Gaussian input file |
| Rappe3-9-2.log | 2MB | chemical/x-gaussian-log | Gaussian log file |
| Rappe3.fchk | 2MB | chemical/x-gaussian-checkpoint | Formatted checkpoint file |
| opt.cml | 3KB | chemical/x-cml | Optimised geometry |
Member of collection / collaboration
| DOI | Description |
|---|---|
| 10.14469/hpc/11051 | 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. TS2 pathway |
Subject Keywords
| Keyword | Value |
|---|---|
| Gibbs_Energy | -3347.581100 |
| inchi | InChI=1S/C4H6BrO2.Na.4H2O/c1-2-3(5)4(2,6)7;;;;;/h2-3,6H,1H3;;4*1H2/t2-,3+,4+;;;;;/m1...../s1 |
| inchikey | VYIPQKZBGVCDKB-PBRAJOLISA-N |