Rappe Rearrangement. BicycloOxirane formation, Sn2, cis, TS3, Na+.4H2O, Def2-TZVPP, G = -3348.724114, DG = 36.4

DOI: 10.14469/hpc/11199 Metadata

Created: 2022-09-22 16:42

Last modified: 2025-03-27 14:16

Author: Henry Rzepa

License: Creative Commons: Public Domain Dedication 1.0

Funding: (none given)

Description

Gaussian 16 (C01) calculation

Files

FilenameSizeTypeDescription
checkpoint.gjf 1KB chemical/x-gaussian-input Gaussian input file
checkpoint.log 772KB chemical/x-gaussian-log Gaussian log file
checkpoint.fchk 14MB chemical/x-gaussian-checkpoint Formatted checkpoint file
opt.cml 3KB chemical/x-cml Optimised geometry

Member of collection / collaboration

DOIDescription
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

KeywordValue
Gibbs_Energy -3348.724114
inchi InChI=1S/C4H6O2.Br.Na.4H2O/c1-3-2-4(3,5)6;;;;;;/h2-3,5H,1H3;;;4*1H2/t3-,4-;;;;;;/m1....../s1
inchikey OONPFAAKRCDHRN-ABNGRBDBSA-N

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