Photoalkylation/-arylation of <i>ortho</i>-Diketones with Unactivated Organic Halides-Reference-Cited by-同舟云学术

Photoalkylation/-arylation of ortho-Diketones with Unactivated Organic Halides

Published:2023-05-22 Issue:21 Volume:25 Page:3847-3852
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Wang Xiao-Yu¹,He Yong-Qin²,Zhou Yi¹,Lu Lin¹,Song Xian-Rong¹^ORCID,Zhou Zhao-Zhao³,Tian Wan-Fa¹,Xiao Qiang¹^ORCID

Affiliation:

1. Key Laboratory of Organic Chemistry of Jiangxi Province, Jiangxi Science & Technology Normal University, Nanchang 330013, P.R. China

2. School of Pharmaceutical Science, Nanchang University, Nanchang 330006, P. R. China

3. College of Chemistry and Food Science, Nanchang Normal University, Nanchang 330013, P. R. China

Funder

Education Department of Jiangxi Province

National Natural Science Foundation of China

Natural Science Foundation of Jiangxi Province

Jiangxi Science and Technology Normal University

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.3c01191

Reference55 articles.

1. Carey, F. A.; Sundberg, R. J. In Advanced Organic Chemistry: Part B: Reactions and Synthesis; Carey, F. A., Sundberg, R. J., Eds. Springer US: Boston, MA, 2007; pp 619–673.

2. Generation of allylic and benzylic organolithium reagents from the corresponding ester, amide, carbonate, carbamate and urea derivatives

3. Indium mediated Barbier reactions of 1,2-diones: a facile synthesis of α-hydroxy ketones

4. Samarium-mediated Barbier reaction of carbonyl compounds

5. High regio- and stereoselective Barbier reaction of carbonyl compounds mediated by NaBF4/Zn (Sn) in waterElectronic supplementary information (ESI) available: spectral data of Barbier-type reaction products and quantum calculation results. See http://www.rsc.org/suppdata/nj/b3/b303187j/

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