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Enantio- and Diastereoselective Synthesis of syn-β-Hydroxy-α-Vinyl Carboxylic Esters via Reductive Aldol Reactions of Ethyl Allenecarboxylate with 10-TMS-9-Borabicyclo[3.3.2]decane and DFT Analysis of the Hydroboration Pathway

[Image: see text] An enantio- and diastereoselective synthesis of syn-β-hydroxy-α-vinyl carboxylate esters 3 via the reductive aldol reaction of ethyl allenecarboxylate (2) with 10-trimethylsilyl-9-borabicyclo[3.3.2]decane (1R, Soderquist’s borane) has been developed. Density functional theory calcu...

Ausführliche Beschreibung

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Bibliographische Detailangaben
Hauptverfasser: Kister, Jeremy, Ess, Daniel H., Roush, William R.
Format: Artigo
Sprache:Inglês
Veröffentlicht: 2013
Schlagworte:
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3849616/
https://ncbi.nlm.nih.gov/pubmed/24138187
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ol4025277
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