Development of the Inverse Sonogashira Reaction for DEL Synthesis.

ACS Med Chem Lett

Pharmaron (Ningbo) Technology Development Co., Ltd., No. 800 Bin-Hai Fourth Road, Hangzhou Bay New Zone, Ningbo 315336, P. R. China.

Published: March 2023

An efficient approach for aryl acetylene DNA-encoded library (DEL) synthesis was developed in this study by transition-metal-mediated inverse Sonogashira reaction of 1-iodoalkyne with boronic acid under ambient conditions, with moderate to excellent conversions and broad substrate adaptability for the first time. Compared to palladium-phosphine, copper iodide performed better in the on-DNA inverse Sonogashira reaction. Interestingly, substrate diversity can be enhanced by first interrogating coupling reagents under copper-promoted conditions, and then revalidating them under palladium-facilitated conditions for those reagents which failed under the former. This complementary validation strategy is particularly well-fitted to any DEL validation studies.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10009795PMC
http://dx.doi.org/10.1021/acsmedchemlett.2c00477DOI Listing

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Development of the Inverse Sonogashira Reaction for DEL Synthesis.

ACS Med Chem Lett

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Pharmaron (Ningbo) Technology Development Co., Ltd., No. 800 Bin-Hai Fourth Road, Hangzhou Bay New Zone, Ningbo 315336, P. R. China.

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