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Enzymatic Cascade Reactions for the Synthesis of Chiral Amino Alcohols from L-lysine
Published on: February 16, 2018
A Sequential Homologation of Alkynes and Aldehydes for Chain Elongation with Optional (13)C-Labeling
Andreas Brunner1, Lukas Hintermann2
1Department Chemie, Technische Universität München, Lichtenbergstr. 4, 85748, Garching bei München, Germany.
Abstract:
Terminal alkynes (RCCH) are homologated by a sequence of ruthenium-catalyzed anti-Markovnikov hydration of alkyne to aldehyde (RCH2CHO), followed by Bestmann-Ohira alkynylation of aldehyde to chain-elongated alkyne (RCH2CCH). Inverting the sequence by starting from aldehyde brings about the reciprocal homologation of aldehydes instead. The use of (13)C-labeled Bestmann-Ohira reagent (dimethyl ((1-(13)C)-1-diazo-2-oxopropyl)phosphonate) for alkynylation provides straightforward access to singly or, through additional homologation, multiply (13) C-labeled alkynes. The labeled alkynes serve as synthetic platform for accessing a multitude of specifically (13)C-labeled products. Terminal alkynes with one or two (13)C-labels in the alkyne unit have been submitted to alkyne-azide click reactions; the copper-catalyzed version (CuAAC) was found to display a regioselectivity of >50,000:1 for the 1,4- over the 1,5-triazine isomer, as shown analytically by (13)C NMR spectroscopy.
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