Catalytic Deprotonative α-Formylation of Heteroarenes by an Amide Base Generated in Situ from Tetramethylammonium Fluoride and Tris(trimethylsilyl)amine-Reference-Cited by-同舟云学术

Catalytic Deprotonative α-Formylation of Heteroarenes by an Amide Base Generated in Situ from Tetramethylammonium Fluoride and Tris(trimethylsilyl)amine

Published:2018-10-29 Issue:4 Volume:23 Page:443-451
ISSN:1083-6160
Container-title:Organic Process Research & Development
language:en
Short-container-title:Org. Process Res. Dev.

Author:

Shigeno Masanori¹^ORCID,Fujii Yuki¹,Kajima Akihisa¹,Nozawa-Kumada Kanako¹^ORCID,Kondo Yoshinori¹

Affiliation:

1. Department of Biophysical Chemistry, Graduate School of Pharmaceutical Science, Tohoku University, Aoba, Sendai 980-8578, Japan

Funder

Sumitomo Foundation

Japan Agency for Medical Research and Development

Japan Society for the Promotion of Science

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.oprd.8b00247

Reference66 articles.

1. The 2×3 Toolbox of Organometallic Methods for Regiochemically Exhaustive Functionalization

2. Deprotonative Metalation Using Ate Compounds: Synergy, Synthesis, and Structure Building

3. Polyfunctional Zinc and Magnesium Organometallics for Organic Synthesis: Some Perspectives

4. CH Bond Functionalization: Emerging Synthetic Tools for Natural Products and Pharmaceuticals

5. Beyond C2 and C3: Transition-Metal-Catalyzed C–H Functionalization of Indole

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