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  • Synthesis of highly substituted oxetanes via [2+2] cycloaddition reactions of allenoates catalyzed by a guanidine Lewis base.

Synthesis of highly substituted oxetanes via [2+2] cycloaddition reactions of allenoates catalyzed by a guanidine Lewis base.

Chemical communications (Cambridge, England) (2013-03-06)
Philipp Selig, Aleksej Turočkin, William Raven
ZUSAMMENFASSUNG

The first synthesis of highly substituted 3-alkyl-oxetan-2-ylidenes from allenoates was developed by using the bicyclic guanidine 1,5,7-triazabicyclo[4.4.0]dec-5-ene (TBD) as an exceptionally active nitrogen Lewis base catalyst.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
Guanidin -hydrochlorid, for molecular biology, ≥99%
Sigma-Aldrich
Guanidin -hydrochlorid, ≥98%
Sigma-Aldrich
Guanidin -hydrochlorid, ≥99% (titration), organic base and chaeotropic agent
Sigma-Aldrich
Guanidin -hydrochlorid -Lösung, Colorless liquid, 7.8 - 8.3 M, pH- 4.5 - 5.5
Sigma-Aldrich
Guanidin -hydrochlorid -Lösung, BioUltra, ~8 M in H2O
Sigma-Aldrich
Guanidin -hydrochlorid, ≥99.0% (AT)
Sigma-Aldrich
Guanidin -hydrochlorid, BioUltra, for molecular biology, ≥99.5% (AT)
Sigma-Aldrich
Trimethylenoxid, 97%
Sigma-Aldrich
Guanidin -sulfat (Salz), 99%