Computational Studies on the Mechanism and Origin of the Different Regioselectivities of Manganese Porphyrin-Catalyzed C–H Bond Hydroxylation and Amidation of Equilenin Acetate-Reference-Cited by-同舟云学术

Computational Studies on the Mechanism and Origin of the Different Regioselectivities of Manganese Porphyrin-Catalyzed C–H Bond Hydroxylation and Amidation of Equilenin Acetate

Published:2020-11-23 Issue:23 Volume:85 Page:14879-14889
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Jin Liyuan¹,Wang Qunmin¹,Chen Xiahe¹,Liu Ning¹,Fang Xiaoli¹,Yang Yun-Fang¹^ORCID,She Yuan-Bin¹^ORCID

Affiliation:

1. College of Chemical Engineering, Zhejiang University of Technology, Hangzhou, Zhejiang 310014, China

Funder

National Natural Science Foundation of China

State Key Laboratory of Green Chemistry-Synthesis Technology, Zhejiang University of Technology

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.0c01444

Reference88 articles.

1. Catalytic C–H functionalization by metalloporphyrins: recent developments and future directions

2. Selective functionalisation of saturated C–H bonds with metalloporphyrin catalysts

3. Oxygen Activation and Radical Transformations in Heme Proteins and Metalloporphyrins

4. Metalloporphyrin Catalyzed C–H Amination

5. Stereoselectivity, Different Oxidation States, and Multiple Spin States in the Cyclopropanation of Olefins Catalyzed by Fe–Porphyrin Complexes

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