Aerobic oxyfunctionalization of alkynes by a bioinspired flavin–metal ion photocatalytic system-Reference-Cited by-同舟云学术

Aerobic oxyfunctionalization of alkynes by a bioinspired flavin–metal ion photocatalytic system

Published:2023 Issue:11 Volume:10 Page:2653-2662
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Shen Duyi¹^ORCID,Zhong Fubi¹,Li Linghui¹,Zhang Haixing¹,Ren Ting¹,Sun Chaoyue¹,Wang Bin²^ORCID,Guo Mian³,Chao Mianran¹,Fukuzumi Shunichi⁴^ORCID

Affiliation:

1. Key Laboratory of Life-Organic Analysis of Shandong Province, School of Chemistry and Chemical Engineering, Qufu Normal University, Qufu 273165, P. R. China

2. School of Chemistry and Chemical Engineering, University of Jinan, Jinan 250022, P. R. China

3. College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, P. R. China

4. Department of Chemistry and Nano Science, Ewha Womans University, Seoul 03760, Republic of Korea

Abstract

α-Keto ketals and benzannulated oxo-spiroketals have been regioselectively synthesized using a Sc3+-coordinated riboflavin tetraacetate photocatalyst with electron-deficient alkynes and alkynediols, respectively.

Funder

National Natural Science Foundation of China

Ministry of Education, Culture, Sports, Science and Technology

Natural Science Foundation of Shandong Province

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/QO/D3QO00375B

Reference67 articles.

1. Benzannulated spiroketal natural products: isolation, biological activity, biosynthesis, and total synthesis