Chiral Cp<sup><i>x</i></sup>Rh<sup>III</sup>-catalyzed enantioselective C–H annulation to access fused tricyclic sulfur-stereogenic and medium-sized aza-heterocycles

Chiral Cp x Rh-catalyzed enantioselective sp 2 C–H bond activation/annulation reactions give S-stereogenic poly-heterocyclic sulfoximines in up to 99% ee. The tricyclic products can be converted into 10-membered S-stereogenic products upon oxidation.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2024-11-15
DOI
https://doi.org/10.1039/d4qo01749h
Citations
9
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
2.25

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article

Chiral CpxRhIII-catalyzed enantioselective C–H annulation to access fused tricyclic sulfur-stereogenic and medium-sized aza-heterocycles

Muhammad Suleman, Yuping Xiong, Shujuan Xu, Zhiyuan Chen
9 citations
Organic Chemistry Frontiers
Catalytic C–H Functionalization Methods
2.25
article

Chiral CpxRhIII-catalyzed enantioselective C–H annulation to access fused tricyclic sulfur-stereogenic and medium-sized aza-heterocycles

Muhammad Suleman, Yuping Xiong, Shujuan Xu, Zhiyuan Chen
article en
9 citations

Abstract

Chiral Cp x Rh-catalyzed enantioselective sp 2 C–H bond activation/annulation reactions give S-stereogenic poly-heterocyclic sulfoximines in up to 99% ee. The tricyclic products can be converted into 10-membered S-stereogenic products upon oxidation.

Organic Chemistry FrontiersVol. 12(2)
Hangzhou City University
National Natural Science Foundation of China
Clean water and sanitation
Openalex Percentile: Top 12%
Catalytic C–H Functionalization Methods
2.25
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