HDA-2+4 mechanism, Product, trans + HCl, p=OMe -1383.430568
DOI: 10.14469/hpc/4089 Metadata
Created: 2018-04-19 12:42
Last modified: 2019-02-05 16:48
License: Creative Commons: Public Domain Dedication 1.0
Funding: (none given)
Description
Gaussian Calculation
Files
Filename | Size | Type | Description |
---|---|---|---|
input.gjf | 2KB | chemical/x-gaussian-input | Gaussian input file |
gaussian.log | 1MB | chemical/x-gaussian-log | Gaussian log file |
checkpoint.fchk | 38MB | chemical/x-gaussian-checkpoint | Formatted checkpoint file |
cml.xml | 5KB | application/xml | Optimised geometry |
wavefunction.wfn | 0 | chemical/x-gaussian-wavefunction | 'Wavefunction' |
Member of collection / collaboration
DOI | Description |
---|---|
10.14469/hpc/3985 | FAIR data for Acid Catalyzed Furanochromane Formation â Stepwise via an Oxonium Prins Reaction or Concerted via a Hetero Diels Alder Reaction? HCl catalyzed trans stereochemistry |
Subject Keywords
Keyword | Value |
---|---|
inchi | InChI=1S/C18H18O3.ClH/c1-19-13-8-6-12(7-9-13)17-15-10-11-20-18(15)14-4-2-3-5-16(14)21-17;/h2-9,15,17-18H,10-11H2,1H3;1H/t15-,17-,18-;/m1./s1 |
inchi | InChI=1S/C18H19ClO3/c1-20-13-8-6-12(7-9-13)18-15-10-11-21-17(15)14-4-2-3-5-16(14)22(18)23-19/h2-9,15,17-18H,10-11H2,1H3/t15-,17+,18+/m0/s1 |
inchi | InChI=1S/C18H18O3.ClH/c1-19-13-8-6-12(7-9-13)17-15-10-11-20-18(15)14-4-2-3-5-16(14)21-17;/h2-9,15,17-18H,10-11H2,1H3;1H/t15-,17-,18-;/m1./s1 |
inchikey | HBHGXHAACXORRP-GUCVWDHMSA-N |
inchikey | QNRZUEFZIZBBKV-CGTJXYLNSA-N |
inchikey | HBHGXHAACXORRP-GUCVWDHMSA-N |