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Regioselective allene synthesis and propargylations with propargyl diethanolamine boronates.

Organic letters (2009-11-03)
Daniel R Fandrick, Jonathan T Reeves, Zhulin Tan, Heewon Lee, Jinhua J Song, Nathan K Yee, Chris H Senanayake
ZUSAMMENFASSUNG

The utility of propargyl diethanolamine boronates as reagents for the preparation of allenes and homopropargylic alcohols is presented. Protonolysis with TFA and electrophilic substitution with N-halosuccinimides proceeded with inversion to provide the corresponding allene in high yield and regioselectivity. Alternatively, the propargylation of aldehydes was achieved with use of the in situ generated lithiated complex.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
Diethanolamin, reagent grade, ≥98.0%
Sigma-Aldrich
Diethanolamin, BioUltra, ≥99.5% (GC)
Sigma-Aldrich
Diethanolamin, puriss. p.a., ACS reagent, ≥99.0% (GC)
Sigma-Aldrich
Diethanolamin, ACS reagent, ≥98.5%
Sigma-Aldrich
Diethanolamin -hydrochlorid, 98%
Supelco
Diethanolamin, analytical standard