DTBP-promoted site-selective α-alkoxyl C–H functionalization of alkyl esters: synthesis of 2-alkyl ester substituted chromanones-Reference-Cited by-同舟云学术

DTBP-promoted site-selective α-alkoxyl C–H functionalization of alkyl esters: synthesis of 2-alkyl ester substituted chromanones

Published:2021 Issue:20 Volume:19 Page:4520-4528
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Yu Jin-Tao¹²³⁴⁵^ORCID,Li Yiting¹²³⁴⁵,Chen Rongzhen¹²³⁴⁵,Yang Zixian¹²³⁴⁵,Pan Changduo¹²³⁴⁵^ORCID

Affiliation:

1. School of Petrochemical Engineering

2. Jiangsu Key Laboratory of Advanced Catalytic Materials & Technology

3. Changzhou University

4. Changzhou 213164

5. P. R. China

Abstract

DTBP-promoted site-selective α-alkoxyl C–H functionalization of alkyl esters towards 2-alkyl ester substituted chromanones via a radical pathway was developed.

Funder

National Natural Science Foundation of China

Qinglan Project of Jiangsu Province of China

Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology Department

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/OB/D1OB00605C

Reference46 articles.

1. Controlling Site Selectivity in Palladium-Catalyzed C–H Bond Functionalization

2. Transition Metal-Catalyzed C–H Amination: Scope, Mechanism, and Applications

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4. Innate and Guided C–H Functionalization Logic

5. From Pd(OAc)2 to Chiral Catalysts: The Discovery and Development of Bifunctional Mono-N-Protected Amino Acid Ligands for Diverse C–H Functionalization Reactions

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