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Merck

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
ABSTRAKT

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.

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