Catalyst-free photodecarbonylation of ortho-amino benzaldehyde-Reference-Cited by-同舟云学术

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Catalyst-free photodecarbonylation of ortho-amino benzaldehyde

Published:2020 Issue:11 Volume:22 Page:3421-3426
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Zhou Jingwei¹²³⁴⁵^ORCID,Li Lamei¹²³⁴⁵,Wang Songping¹²³⁴⁵,Yan Ming⁶⁷⁸⁹⁵^ORCID,Wei Wentao¹²³⁴⁵^ORCID

Affiliation:

1. Institute of Clinical Pharmacology

2. Science and Technology Innovation Center

3. Guangzhou University of Chinese Medicine

4. Guangzhou 510405

5. China

6. Institute of Drug Synthesis and Pharmaceutical Process

7. School of Pharmaceutical Sciences

8. Sun Yat-sen University

9. Guangzhou 510006

Abstract

Decarbonylation is easily achieved with visible light irradiation by introducing a tertiary amine into the ortho-position of the aldehyde group.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Guangdong Province

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/GC/D0GC01256D

Reference51 articles.

1. Asymmetric Catalysis Special Feature Part II: Mo-catalyzed asymmetric olefin metathesis in target-oriented synthesis: Enantioselective synthesis of (+)-africanol

2. Biomimetic Synthesis of Antimalarial Naphthoquinones

3. Rh-catalyzed C–C bond cleavage by transfer hydroformylation

4. Synthetic and Mechanistic Studies of the Retro-Claisen Rearrangement 4. An Application to the Total Synthesis of (+)-Laurenyne

5. Rh(I)-catalyzed decarbonylation synthesis of carbazoles via C–N cleavage

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