Straightforward and Efficient Deuteration of Terminal Alkynes with Copper Catalysis

DOI: 10.14469/hpc/12314 Metadata

Created: 2023-02-27 20:33

Last modified: 2024-11-27 17:00

Author: Silvia Diez-Gonzalez

License: Creative Commons: Public Domain Dedication 1.0

Funding: (none given)

Co-author: Silvia Diez-Gonzalez

Description

The mild and effective preparation of deuterated organic molecules is an active area of research due to their important applications. Herein, we report an air-stable and easy to access copper(I) complex as catalyst for the deuteration of mono-substituted alkynes. Reactions were carried out in technical solvents and in the presence of air, to obtain excellent deuterium incorporation in a range of functionalized alkynes.

Members

DOIDescription
10.14469/hpc/12319 1a-D, 1-Deutero-oct-1-yne
10.14469/hpc/12323 1e-D, 4-Deutero-2-methylbut-3-yn-2-ol
10.14469/hpc/12324 1f-D, 3-Deutero-1,1-diphenylprop-2-yn-1-ol
10.14469/hpc/12326 1h-D, Deutero(trimethylsilyl)acetylene
10.14469/hpc/12320 1b-D, 1,8-Deutero-octa-1,7-diyne
10.14469/hpc/12321 1c-D, 5-Chloro-1-deutero-pent-1-yne
10.14469/hpc/12322 1d-D, 5-Deuterohex-5-yn-1-ol
10.14469/hpc/12325 1g-D, 1-Deutero-ethynyl-1-cyclohexanol
10.14469/hpc/12327 1i-D, Deutero(triphenylsilyl)acetylene
10.14469/hpc/12328 1j-D, 3-Deutero N,N-diethyl-prop-2-ynyl amine
10.14469/hpc/12329 1k-D, Tris(prop-2-ynyl-3-deutero)amine
10.14469/hpc/12330 1l-D, 2-(Prop-2-ynyl-3-deutero)isoindoline-1,3-dione
10.14469/hpc/12331 1m-D, Phenyl(prop-2-ynyl-3-deutero)sulfane
10.14469/hpc/12333 1n-D, Ethyl Deuteropropiolate
10.14469/hpc/12334 1o-D, Dimethyl-2-(3-deutero-prop-2-ynyl) (deutero)malonate
10.14469/hpc/12335 1p-D, 1-Deutero-3,3-diethoxyprop-1-yne
10.14469/hpc/12336 1q-D, 1-Deutero-p-tolylacetylene
10.14469/hpc/12337 1r-D, 1-Deutero-p-anisylacetylene
10.14469/hpc/12338 1s-D, 1-Bromo-4-(deuteroethynyl)-benzene
10.14469/hpc/12339 1t-D, 1,3-Bis(deuteroethynyl)benzene
10.14469/hpc/12340 1u-D, 3-(Deuteroethynyl)pyridine
10.14469/hpc/12341 1v-D, 2-(Deuteroethynyl)pyridine

Associated DOIs

Current dataset ...DOIDescription
References 10.3390/catal13040648 Published reference

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