Simplified Modular Access to Enantiopure 1,2-Aminoalcohols via Ni- Electrocatalytic Decarboxylative...
Simplified Modular Access to Enantiopure 1,2-Aminoalcohols via Ni- Electrocatalytic Decarboxylative Arylation
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Washington: American Chemical Society
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English
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Washington: American Chemical Society
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Contents
Chiral aminoalcohols are omnipresent in bioactive compounds. Conventional strategies to access this motif involve multiple-step reactions to install requisite functionalities stere- oselectively using conventional polar bond analysis. This study re- veals that a simple chiral oxazolidine-based carboxylic acid can be readily transformed to substitut...
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Full title
Simplified Modular Access to Enantiopure 1,2-Aminoalcohols via Ni- Electrocatalytic Decarboxylative Arylation
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TN_cdi_proquest_journals_2901563534
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2901563534
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E-ISSN
2573-2293
DOI
10.26434/chemrxiv-2023-rl75s
