A unifying mechanism for the rearrangement of vinyl allene oxide geometric isomers to cyclopentenones.

González-Pérez AB, Grechkin A, de Lera AR

Open source

DOI
10.1039/c4ob00562g
Published
2014 Oct 21
Container
Organic & biomolecular chemistry
Publisher
Not recorded
Open access
unknown

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BibTeX

@article{allodium:10.1039/c4ob00562g,
  title = {A unifying mechanism for the rearrangement of vinyl allene oxide geometric isomers to cyclopentenones.},
  author = {González-Pérez AB and Grechkin A and de Lera AR},
  year = {2014},
  journal = {Organic \& biomolecular chemistry},
  doi = {10.1039/c4ob00562g},
  url = {https://doi.org/10.1039/c4ob00562g}
}

RIS

TY  - JOUR
TI  - A unifying mechanism for the rearrangement of vinyl allene oxide geometric isomers to cyclopentenones.
AU  - González-Pérez AB
AU  - Grechkin A
AU  - de Lera AR
PY  - 2014
JO  - Organic & biomolecular chemistry
DO  - 10.1039/c4ob00562g
UR  - https://doi.org/10.1039/c4ob00562g
ER  - 

APA

AB, G., A, G., & AR, D. L. (2014). A unifying mechanism for the rearrangement of vinyl allene oxide geometric isomers to cyclopentenones.. Organic & biomolecular chemistry. https://doi.org/10.1039/c4ob00562g

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