[2+2+2] Cycloadditions of siloxy alkynes with 1,2-diazines: from reaction discovery to identification of an antiglycolytic chemotype.

Angew Chem Int Ed Engl

Chicago Tri-Institutional Center for Chemical Methods and Library Development, Department of Chemistry, The University of Chicago, Chicago, IL 60637 (USA).

Published: December 2013

Cycloaddition uncovered: The title reaction produces novel polycyclic compounds with high efficiency and excellent diastereoselectivity under mild reaction conditions. A small-molecule library, synthesized using this reaction, yielded a novel chemotype which inhibited glycolytic ATP production by blocking glucose uptake in CHO-K1 cells. DMF=N,N-dimethylformamide, Tf=trifluoromethanesulfonyl, TIPS=triisopropylsilyl.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3996828PMC
http://dx.doi.org/10.1002/anie.201305711DOI Listing

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