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An efficient process for recycle S-valsartan from the racemic coproduct via diastereomeric crystallization by using natural dehydroabietylamine as the enantioselective recognition media
Research article (Separation and Purification Technology, 2021) · cited 12× · AI/ML
An efficient process for recycle S-valsartan from the racemic coproduct via diastereomeric crystallization by using natural dehydroabietylamine as the enantioselective recognition media
Summary
An efficient process for recycle S-valsartan from the racemic coproduct via diastereomeric crystallization by using natural dehydroabietylamine as the enantioselective recognition media is a scholarly article[1].
Key Facts
An efficient process for recycle S-valsartan from the racemic coproduct via diastereomeric crystallization by using natural dehydroabietylamine as the enantioselective recognition media's instance of is recorded as scholarly article[2].
References
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Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.
APA4ort.xyz Knowledge Graph. (2026). An efficient process for recycle S-valsartan from the racemic coproduct via diastereomeric crystallization by using natural dehydroabietylamine as the enantioselective recognition media. Retrieved May 24, 2026, from https://4ort.xyz/entity/an-efficient-process-for-recycle-s-valsartan-from-the-racemic-coproduct-via-diastereomeric-crystallization-by-using-natu
MLA“An efficient process for recycle S-valsartan from the racemic coproduct via diastereomeric crystallization by using natural dehydroabietylamine as the enantioselective recognition media.” 4ort.xyz Knowledge Graph, 4ort.xyz, 24 May. 2026, https://4ort.xyz/entity/an-efficient-process-for-recycle-s-valsartan-from-the-racemic-coproduct-via-diastereomeric-crystallization-by-using-natu.
BibTeX@misc{4ortxyz_an-efficient-process-for-recycle-s-valsartan-from-the-racemic-coproduct-via-diastereomeric-crystallization-by-using-natu_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{An efficient process for recycle S-valsartan from the racemic coproduct via diastereomeric crystallization by using natural dehydroabietylamine as the enantioselective recognition media}}, year = {2026}, url = {https://4ort.xyz/entity/an-efficient-process-for-recycle-s-valsartan-from-the-racemic-coproduct-via-diastereomeric-crystallization-by-using-natu}, note = {Accessed: 2026-05-24}}
LLM promptAccording to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): An efficient process for recycle S-valsartan from the racemic coproduct via diastereomeric crystallization by using natural dehydroabietylamine as the enantioselective recognition media — https://4ort.xyz/entity/an-efficient-process-for-recycle-s-valsartan-from-the-racemic-coproduct-via-diastereomeric-crystallization-by-using-natu (retrieved 2026-05-24)
