Oxidation of NOBINs Toward α-Spiropyrrolidones

While the oxidation of phenols and BINOLs is well documented to lead to a broad range of useful organic scaffolds, that of NOBINs is far less explored. We investigate herein their oxidation with a number of standard chemical oxidants, leading upon skeletal rearrangement to the corresponding α-spiropyrrolidones, which represent a rare and highly valuable heterocyclic core.

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Publication Details

Journal
Organic Letters
Published
2024-09-03
DOI
https://doi.org/10.1021/acs.orglett.4c02499
Citations
1
Primary Topic
Axial and Atropisomeric Chirality Synthesis
Type
article
Field-Weighted Citation Impact
0.25

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article

Oxidation of NOBINs Toward α-Spiropyrrolidones

Iris M. Oppel, Yun Yang, Ben Ebel, Frédéric W. Patureau
1 citations
Organic Letters
Axial and Atropisomeric Chirality Synthesis
0.25
article

Oxidation of NOBINs Toward α-Spiropyrrolidones

Iris M. Oppel, Yun Yang, Ben Ebel, Frédéric W. Patureau
article en
1 citations

Abstract

While the oxidation of phenols and BINOLs is well documented to lead to a broad range of useful organic scaffolds, that of NOBINs is far less explored. We investigate herein their oxidation with a number of standard chemical oxidants, leading upon skeletal rearrangement to the corresponding α-spiropyrrolidones, which represent a rare and highly valuable heterocyclic core.

Organic LettersVol. 26(36)
RWTH Aachen University (DE)
China Scholarship Council
Openalex Percentile: Top 49%
Axial and Atropisomeric Chirality Synthesis
0.25
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