Light‐driven strategies for stereocenter editing

Abstract The more functional groups a molecule contains, the more likely a reaction is going to fail. Despite this challenge, researchers have developed mild methods to invert a stereocenter late in the synthesis, opening the door to new chemical structures.

Authors

Publication Details

Journal
Nachrichten aus der Chemie
Published
2025-12-01
DOI
https://doi.org/10.1002/nadc.20254153841
Primary Topic
Photochromic and Fluorescence Chemistry
Type
article
Field-Weighted Citation Impact
0.00
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article

Light‐driven strategies for stereocenter editing

Kapil Medhi, Alicia Casitas
Nachrichten aus der Chemie
Photochromic and Fluorescence Chemistry
article

Light‐driven strategies for stereocenter editing

Kapil Medhi, Alicia Casitas
article en

Abstract

Abstract The more functional groups a molecule contains, the more likely a reaction is going to fail. Despite this challenge, researchers have developed mild methods to invert a stereocenter late in the synthesis, opening the door to new chemical structures.

Nachrichten aus der ChemieVol. 73(12)
Openalex Percentile: Top 69%
Photochromic and Fluorescence Chemistry
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Light‐driven strategies for stereocenter editing — Kapil Medhi, Alicia Casitas · Nachrichten aus der Chemie (2025) | TGRS Research Map | TGRS