Stereochemical Inversion
Stereochemical Inversion is a stereochemical process in which the spatial arrangement of atoms around a chiral center in a herbicide molecule is reversed, leading to the conversion of one enantiomer into its mirror-image counterpart, thereby potentially altering its biological activity, environmental fate, and selectivity in target and non-target organisms.
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2017–2026
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386
Patrick D. Pohlhaus, Shanina D. Sanders, Andrew T. Parsons et al. · Journal of the American Chemical Society · 2008 · 371 citations
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Czech Academy of Sciences, Institute of Organic Chemistry and Biochemistry, Czechia
4 publications · 49 citations
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Centre National de la Recherche Scientifique
Paris, France
11 h-index
45 publications
1.8K citations

University of Szeged
Szeged, Hungary
8 h-index
20 publications
544 citations
Columbia University
New York, United States
6 h-index
23 publications
1.7K citations

University of Manchester
Manchester, United Kingdom
6 h-index
22 publications
828 citations

Hokkaido University
Sapporo, Japan
5 h-index
16 publications
657 citations

Kyoto University
Kyoto, Japan
5 h-index
19 publications
393 citations
University of Oxford
Oxford, United Kingdom
5 h-index
18 publications
455 citations
The University of Tokyo
Tokyo, Japan
4 h-index
15 publications
723 citations
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JACS · 59 publications · 3.3K citations
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JOC · 18 publications · 638 citations
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