Enantiospecific Alkynylation of Alkylboronic Esters |
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| Authors: | Dr. Yahui Wang Dr. Adam Noble Dr. Eddie L. Myers Prof. Dr. Varinder K. Aggarwal |
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| Affiliation: | School of Chemistry, University of Bristol, Bristol, UK |
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| Abstract: | Enantioenriched secondary and tertiary alkyl pinacolboronic esters undergo enantiospecific deborylative alkynylation through a Zweifel‐type alkenylation followed by a 1,2‐elimination reaction. The process involves use of α‐lithio vinyl bromide or vinyl carbamate species, for which application to Zweifel‐type reactions has not previously been explored. The resulting functionalized 1,1‐disubstituted alkenes undergo facile base‐mediated elimination to generate terminal alkyne products in high yield and excellent levels of enantiospecificity over a wide range of pinacolboronic ester substrates. Furthermore, along with terminal alkynes, internal and silyl‐protected alkynes can be formed by simply introducing a suitable carbon‐ or silicon‐based electrophile after the base‐mediated 1,2‐elimination reaction. |
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| Keywords: | alkynes alkynylation boronic esters synthetic methods |
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