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C–H Methylation of Heteroarenes Inspired by Radical SAM Methyl Transferase

[Image: see text] A practical C–H functionalization method for the methylation of heteroarenes is presented. Inspiration from Nature’s methylating agent, S-adenosylmethionine (SAM), allowed for the design and development of zinc bis(phenylsulfonylmethanesulfinate), or PSMS. The action of PSMS on a h...

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Autores principales: Gui, Jinghan, Zhou, Qianghui, Pan, Chung-Mao, Yabe, Yuki, Burns, Aaron C., Collins, Michael R., Ornelas, Martha A., Ishihara, Yoshihiro, Baran, Phil S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3988686/
https://www.ncbi.nlm.nih.gov/pubmed/24611732
http://dx.doi.org/10.1021/ja5007838
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author Gui, Jinghan
Zhou, Qianghui
Pan, Chung-Mao
Yabe, Yuki
Burns, Aaron C.
Collins, Michael R.
Ornelas, Martha A.
Ishihara, Yoshihiro
Baran, Phil S.
author_facet Gui, Jinghan
Zhou, Qianghui
Pan, Chung-Mao
Yabe, Yuki
Burns, Aaron C.
Collins, Michael R.
Ornelas, Martha A.
Ishihara, Yoshihiro
Baran, Phil S.
author_sort Gui, Jinghan
collection PubMed
description [Image: see text] A practical C–H functionalization method for the methylation of heteroarenes is presented. Inspiration from Nature’s methylating agent, S-adenosylmethionine (SAM), allowed for the design and development of zinc bis(phenylsulfonylmethanesulfinate), or PSMS. The action of PSMS on a heteroarene generates a (phenylsulfonyl)methylated intermediate that can be easily separated from unreacted starting material. This intermediate can then be desulfonylated to the methylated product or elaborated to a deuteriomethylated product, and can divergently access medicinally important motifs. This mild, operationally simple protocol that can be conducted in open air at room temperature is compatible with sensitive functional groups for the late-stage functionalization of pharmacologically relevant substrates.
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spelling pubmed-39886862014-04-17 C–H Methylation of Heteroarenes Inspired by Radical SAM Methyl Transferase Gui, Jinghan Zhou, Qianghui Pan, Chung-Mao Yabe, Yuki Burns, Aaron C. Collins, Michael R. Ornelas, Martha A. Ishihara, Yoshihiro Baran, Phil S. J Am Chem Soc [Image: see text] A practical C–H functionalization method for the methylation of heteroarenes is presented. Inspiration from Nature’s methylating agent, S-adenosylmethionine (SAM), allowed for the design and development of zinc bis(phenylsulfonylmethanesulfinate), or PSMS. The action of PSMS on a heteroarene generates a (phenylsulfonyl)methylated intermediate that can be easily separated from unreacted starting material. This intermediate can then be desulfonylated to the methylated product or elaborated to a deuteriomethylated product, and can divergently access medicinally important motifs. This mild, operationally simple protocol that can be conducted in open air at room temperature is compatible with sensitive functional groups for the late-stage functionalization of pharmacologically relevant substrates. American Chemical Society 2014-03-10 2014-04-02 /pmc/articles/PMC3988686/ /pubmed/24611732 http://dx.doi.org/10.1021/ja5007838 Text en Copyright © 2014 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html)
spellingShingle Gui, Jinghan
Zhou, Qianghui
Pan, Chung-Mao
Yabe, Yuki
Burns, Aaron C.
Collins, Michael R.
Ornelas, Martha A.
Ishihara, Yoshihiro
Baran, Phil S.
C–H Methylation of Heteroarenes Inspired by Radical SAM Methyl Transferase
title C–H Methylation of Heteroarenes Inspired by Radical SAM Methyl Transferase
title_full C–H Methylation of Heteroarenes Inspired by Radical SAM Methyl Transferase
title_fullStr C–H Methylation of Heteroarenes Inspired by Radical SAM Methyl Transferase
title_full_unstemmed C–H Methylation of Heteroarenes Inspired by Radical SAM Methyl Transferase
title_short C–H Methylation of Heteroarenes Inspired by Radical SAM Methyl Transferase
title_sort c–h methylation of heteroarenes inspired by radical sam methyl transferase
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3988686/
https://www.ncbi.nlm.nih.gov/pubmed/24611732
http://dx.doi.org/10.1021/ja5007838
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